<i>Lignosus rhinocerus</i> (Cooke) Ryvarden: A Medicinal Mushroom That Stimulates Neurite Outgrowth in PC-12 Cells

Eik, Lee-Fang; Naidu, Murali; David, Pamela; Wong, Kah-Hui; Tan, Yee-Shin; Sabaratnam, Vikineswary

doi:https://doi.org/10.1155/2012/320308

Evidence-Based Complementary and Alternative Medicine

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Abstract Introduction Methods Results and Discussion Conclusion Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2012 | Article ID 320308 | https://doi.org/10.1155/2012/320308

Lignosus rhinocerus (Cooke) Ryvarden: A Medicinal Mushroom That Stimulates Neurite Outgrowth in PC-12 Cells

Lee-Fang Eik,^1,2Murali Naidu,^1,3Pamela David,^1,3Kah-Hui Wong,^1,2Yee-Shin Tan,^1,2and Vikineswary Sabaratnam^1,2

Academic Editor: José Luis Ríos

Received16 Jun 2011

Revised06 Sept 2011

Accepted07 Sept 2011

Published06 Dec 2011

Abstract

A national treasure mushroom, Lignosus rhinocerus, has been used to treat variety of ailments by local and indigenous communities in Malaysia. The aim of this study was to investigate the potential of the most valuable part of L. rhinocerus, the sclerotium, on neurite outgrowth activity by using PC-12Adh cell line. Differentiated cells with one thin extension at least double the length of the cell diameter were scored positive. Our results showed that aqueous sclerotium L. rhinocerus extract induced neurite outgrowths of 24.4% and 42.1% at 20 μg/mL (w/v) of aqueous extract alone and a combination of 20 μg/mL (w/v) aqueous extract and 30 ng/mL (w/v) of NGF, respectively. Combination of NGF and sclerotium extract had additive effects and enhanced neurite outgrowth. Neuronal differentiation was demonstrated by indirect immunofluorescence of neurofilament protein. Aqueous sclerotium extract contained neuroactive compounds that stimulated neurite outgrowth in vitro. To our knowledge this is the first report on neurite-stimulating activities of L. rhinocerus.

1. Introduction

Formation of central nervous system (CNS) network requires active axonal elongation and systematic explorations activity of environment by growing of axons in order to be directed to their correct target [1]. Neuronal cells are able to sense the surrounding and form branches in response to molecular information from extracellular milieu that instruct the maturation process and induce neurite regeneration in pathological situations such as trauma or degenerative diseases [1]. Neurite outgrowth in cultured neurons is considered as an indication of neuroregenerative potential [2].

Extension and remodeling of neurites play essential roles in development and neuronal plasticity regulated by neuroserpin [3]. Cultured rat pheochromocytoma PC-12 cells have been used extensively as an in vitro model system for investigation of neuronal differentiation. Epidermal growth factor (EGF) and nerve growth factor (NGF) both activate extracellular signal-regulated kinase (ERK) and p38 mitogen-activated protein kinase (MAPK) [4]. But PC-12 cells only respond to neurotrophin NGF and differentiate into sympathetic neuron phenotype and extending axon-like processes called neurites [3]. This serves as an excellent model to study the effects of molecules both synthetic and natural that will stimulate the outgrowth of neurites.

Of the many diseases that threaten humans, neurodegenerative diseases can be very traumatic as one ages. Neurohealth is the concern for the predicted silver tsunami to hit humans—the aging tsunami is projected to be 80–90 million of 65-plus population in 2050 [5]. Why the concern? Alzheimer and neurogenerative diseases are high on the list of chronic diseases of the aged. Alzheimer’s disease is primarily a disorder of aging with loss of cognitive function. This disease is characterized biologically by the death of neurons in the forebrain, hippocampus, and cerebral cortex accompanied by the presence of amyloid deposition.

Many of the drugs in the market only delay further deterioration and do not reverse the damage done to cognitive functions. The search is now for small molecules that can cross the brain-blood and induce the production of nerve growth factor (NGF), a family of proteins responsible for maintenance, survival, and regeneration of neurons during adult life. It has been shown that NGF absence causes an Alzheimer’s like symptoms in the adult brain of mice. We may have to turn to nature to prevent or reduce the severity of nerve-related diseases as we age. Prevention will be definitely better than cure. Many plants and spices such as turmeric are said to help. For example, in India, it is noted that Alzheimer among the older generation is not in alarming numbers. The regular consumption of spices including turmeric and pepper may be the reason and currently this is actively been studied. Currently mushrooms are also being investigated as sources of NGF stimulators.

Mushroom, a macrofungus that has either culinary or medicinal properties, has a visible fruiting body. Culinary mushrooms have been known as famous appetizing and nutritious food all over the world. Historically, medicinal mushrooms used by different tribes are best documented in the eastern world.

In Malaysia, several macrofungi are used by the Malays, Chineses, and indigenous communities for treatment of variety ailments. Lignosus rhinocerus has been singled out as one of the most potent mushrooms for medicinal purposes dating to the 1700s by Tuan Haji Mat Yusop, a Malay in Pahang [6, 7]. Lignosus rhinocerus is a unique “National Treasure” that can only be found in a small geographic region encompassing South China, Thailand, Malaysia, Indonesia, Philippines, Papua New Guinea, New Zealand, and Australia [6]. Lignosus rhinocerus (Cooke) Ryvarden is also known as “cendawan susu rimau” in Malay language or Tiger’s Milk mushroom in English. The medicinal properties recorded by ethno-mycological surveys are yet to be validated scientifically.

Lignosus rhinocerus has more than 15 medicinal uses. Different natives use it as an antipruritic, antipyretic, general tonic, starve off hunger, cancer, food poisoning, swollen breasts [7], fever, cough, asthma, wound healing, and others [6]. Although this mushroom has been recorded to have a number medicinal properties, usage is limited due to unavailability of the mushroom. The underground fungus tuber or sclerotium is the part with medicinal value and it can only be noticed when the fruiting body sprouts out from the ground when nature calls. Recently, efforts made to cultivate this medicinal mushroom have been successful [8] and the mushrooms are now available for scientific studies.

The aim of the study was to assess the presence of active agents in aqueous extract of L. rhinocerus sclerotium that can stimulate neurite outgrowth in PC-12 and the enhancement of neurite outgrowth with the combination of NGF and aqueous extract in PC-12 cells. Quantitative morphological methods and neurofilament formation were used to study the differentiation effects on neurite outgrowth activities in PC-12 cell line. To our knowledge, this is the first report on the application of sclerotium of L. rhinocerus in neurite outgrowth stimulation activity.

2. Methods

2.1. Preparation of Aqueous Extract Sclerotium

Lignosus rhinocerus sclerotium freeze-dried powder was from Dr. Tan Chon Seng of Malaysian Agricultural Research and Development Institute (MARDI). The aqueous extraction method was modified by Wong et al. [9]. Sclerotium powder was weighed; distilled water at a ratio of 1 : 20 (w/v) was added and left for 24 hr at 27 ± 2°C at 150 rpm. Then the mixture was double boiled for 30 min, cooled, and filtered through Whatman filter paper No. 4. The aqueous extract was then freeze-dried at −50 ± 2°C for 48 hr and stored in airtight bottles at −40°C prior to assay.

2.2. In Vitro Cell Culture

PC-12 cell line, derived from transplantable rat pheochromocytoma, has been widely used as neuronal model because it proliferates in growth medium, and stop proliferating and differentiate into neuron-like cells as they respond to NGF [10]. The cell line has been used to study mechanisms of action of neurotoxicants and potential of chemical to alter neurite differentiation [11]. PC-12 cells are grown as floating clusters and few scattered lightly attached cells; therefore adherent variant (PC-12Adh) was designed to improve cell attachment on flask.

PC-12Adh was chosen for this study because it is NGF-dependent and does not synthesize epinephrine. PC-12 cell line was purchased from American Type Culture Collection (Cat #: CRL-1721.1) and only early passage cells were used in this study. The cells were cultured in ATCC-formulated F-12K Medium (Kaighn’s Modification of Ham’s F-12 Medium) supplemented with 2.5% (v/v) fetal bovine serum and 15% (v/v) horse serum with final pH 6.8–7.2 and incubated in 5% CO₂ humidified incubator at 37 ± 2°C [12]. The cells were subcultured every 2 to 3 days as needed. PC-12 cells tend to form clusters and clumps. For subculturing, cells were detached from culture flask by scraping and this forceful aspiration was employed to break up cell clusters [13]. For storage, the cells were frozen in complete F-12K medium with 5% (v/v) dimethylsulfoxide (DMSO) [10].

2.3. Neurite Stimulation Activity Assay

Cells were cultured for 2 to 3 days until 60–70% confluent prior to assay. They were plated into 12-well plates at cell density of 5 × 10⁴ cells per well in complete F-12K medium with concentrations 1 to 500 μg/mL (w/v) of sclerotium aqueous extract. Concentrations of NGF-7S from murine submaxillary gland (Sigma, St. Louis, MO, USA) ranging from 10 ng/mL (w/v) to 100 ng/mL (w/v) were tested to examine the optimum concentration for neurite stimulation activity. The optimum concentration was used as positive control for the following assays. Cells in complete F-12K medium without treatment served as negative control. Freeze-dried aqueous extracts were diluted to various concentration with sterilized distilled water. After the preliminary test, optimum concentration of the sclerotium aqueous extract in combination with NGF ranging from 10 ng/mL (w/v) to 50 ng/mL (w/v) was tested to evaluate synergistic interaction, if any, between sclerotium aqueous extract and NGF. Assay plates were incubated at 37 ± 2°C in a 5% CO₂-humidified incubator. Differentiation activity of cells in terms of neurite outgrowth and branching was observed after 48 hr of incubation at 37 ± 2°C in 5% CO₂-humidified incubator.

2.4. Neurites Scoring

A cell was scored positive for bearing neurites if it has a thin neurite extension that double the length of the cell body diameter. Morphology of the cells is polygonal. Cells with irregular patterns such as sheet-like spreading cells, rare radially oriented possess, and apparently arising by “shrink-age” were excluded [9, 12] and cell clumps with more than five cells in a clump were excluded [9]. Ten fields per well were randomly examined and photographed under Nikon Eclipse TS100 with 10 × 10.25 Nikon objective and captured with Nikon DS-Fi1 camera and Nikon’s Imaging Software, NIS-Elements. The percentage of neurite-bearing cells were quantified by scoring total number of neurite-bearing cells and total number of viable cells in 10 microscopic fields with average of 200 to 300 cells per well.

2.5. Immunofluorescence Staining of Neurofilaments

Immunofluorescence staining of neurofilament protein was carried out according to the method of Schimmelpfeng et al. [18]. Cells were seeded onto 6-well plates where each well contained two sterilized coverslips and incubated for 2 days at 37 ± 2°C in a 5% CO₂-humidified incubator. On the day of experiment cells were 20% to 50% confluent and were fixed with 4% parafamaldehyde at room temperature for 20 min. The cells were then incubated with primary antibody, anti-neurofilament 200 antibody produced in rabbit (1 : 80 dilution in blocking buffer, Sigma, St. Louis, MO, USA) at room temperature for 1 hr, washed with washing buffer, and followed by further reaction with the secondary antibody, Fluorophore-conjugated secondary antibody, Anti-Rabbit IgG-Fluorescein isothiocyanate (FITC) antibody produced in sheep (1 : 80 dilution in blocking buffer, Sigma, St. Louis, MO, USA) at room temperature for 1 to 2 hr in dark. After the same washing procedure, cells were mounted onto slides with aqueous mounting medium, with 4′-6-Diamidino-2-phenylindole (DAPI). DAPI is used to stain nuclei. Finally, slides were observed under Nikon Eclipse 80i microscope under fluorescence illumination using FITC and DAPI filters and images were captured with Nikon’s Imaging Software, NIS-Elements.

2.6. Statistical Analysis

Statistical analysis was performed using the computing environment R (R Development Core Team, 2011) (Vienna, Austria). Permutation test was used to examine the statistical significance of the differences [15]. Confidence intervals provide information on the direction and strength of the effect of the treatment [16, 17]. Therefore, confidence intervals (CIs) for all data were set to 95% () [16].

3. Results and Discussion

3.1. Neurite Stimulation Activity Assay

Neurite outgrowth stimulatory of NGF and aqueous extract of L. rhinocerus was observed after 48 hr of incubation. The uniqueness of PC-12 cell line is that it responds to NGF with a drastic change in its phenotype and cause proliferation, extension of neurite [11]. Figure 1 shows the effect of various concentrations of NGF on neurite stimulation activity of PC-12 cell line.

Figure 1

Percentage of neurite-bearing cells in the cell line PC-12 in response to treatment with various concentrations of NGF (ng/mL). Neurite growth (vertical axis) was quantified as the percentage of cells bearing axodendritic processes longer than two times cell diameters in length. Negative control consists of PC-12 cells in medium only. Data are expressed as means ± standard deviation (). Means with different alphabets show significant difference (Duncan’s Multiple Range Test (DMRT)) (permuted-).

NGF concentration plot (Figure 1) determined the optimum concentration needed to induce maximal neurite outgrowth of PC-12. Percentage of neurite-bearing cell increased when exposed to NGF ranging from negative control which is medium alone to 50 ng/mL (w/v) and decreased when exposed to 60 ng/mL to 100 ng/mL (w/v) of NGF. When the cells were exposed to 50 ng/mL (w/v) of NGF, it showed a maximal effect with an increase of 33% (95% CI: 31–34) or almost five times increase of percentage of neurite-bearing cells compared with medium alone (negative control). Therefore, 50 ng/mL (w/v) of NGF was used as positive control for the subsequent assays.

Aqueous extract of Lignosus rhinocerus showed visible neurite outgrowth activity of PC-12 after 48 hr of incubation (Figure 2). Maximal stimulation was recorded at 24.4% at 20 μg/mL (w/v) with an increase of 15% (95% CI: 13–16) compared to negative control and 2.5% (95% CI: 1–4) higher compared to positive control. Increasing the concentration showed minimal or even negative effect on the number of neurite-bearing cells. There were no significant differences between negative control and addition of extract at concentration of 80 μg/mL (w/v) and 90 μg/mL (w/v). At 100 μg/mL (w/v) when compared to a negative control, a reduction of 1.3% (95% CI: (−2)–(−0.3)) of percentage of neurite-bearing cells was recorded.

Figure 2

Percentage of neurite-bearing cells in the cell line PC-12 incubated with various concentrations of L. rhinocerus aqueous extract (μg/mL). Neurite growth (vertical axis) was quantified as the percentage of cells bearing axodendritic processes longer than two times of cell diameters in length. Negative control consists of PC-12 cells in medium only whereas in positive control the cells were treated with 50 ng/mL (w/w) NGF. Data are expressed as means ± standard deviation (). Means with different alphabets show significant difference (; Duncan’s Multiple Range Test (DMRT)) (permuted-).

From the above results (Figure 2), 20 μg/mL (w/v) of aqueous extract of L. rhinocerus was selected as the optimum concentration for neurite outgrowth activity. The percentage of cells treated with various concentrations of NGF and optimum concentration of aqueous extract at 20 μg/mL (w/v) showed increase in number of neurite-bearing cells compared to cells treated with optimum concentration of aqueous extract alone (Figure 3). This showed that combination of NGF and aqueous extract could enhance stimulation of neurite outgrowth. Optimum concentration of aqueous extract added with 30 ng/mL of NGF showed the best stimulation of neurite outgrowth (42.12%) and a 17% (95% CI: 16–19) increase in neurite-bearing cells compared to aqueous extract alone. Our data showed that the combination of aqueous extract and a lower NGF concentration was able to enhance neurite outgrowth activity comparable to the stimulation activity of a higher concentration of NGF at 50 ng/mL (w/v).

3.2. Immunofluorescence Staining of Neurofilaments

Differentiation of cells is most often assessed by semiquantitative or quantitative morphological methods such as determination of cell size, number of extensions over number of cells, and extent of neurite growth or neurite length [11]. Neurofilaments are dominant intermediate filament found in neuronal cells that provide specific support for developing neurite and maintaining neuronal caliber by formation of filamentous cross-bridge [14]. Another method to study neuronal differentiation is to investigate the formation of neurofilaments, the major structural components of neuron [18]. Regeneration of peroneal neurite can be qualitatively evaluated by immunofluorescence staining of neurofilaments. Anti-neurofilament is a useful immunocytochemical marker for axons [19, 20]. Neuronal cells were treated with aqueous extract at 20 μg/mL (w/v) and incubated for 48 hr. Figures 4(a)–4(c) show immunofluorescene staining of PC-12 cells. After incubation with L. rhinocerus extracts obvious enhancement of neurite outgrowth with extension that double the length of cell body diameter can be observed.

(a)

(b)

(c)

Cold water extraction has been reported to yield lower amount of extract than hot water extraction but it is usually applied in traditional medicine preparation [21]. Most of Basidiomycetes mushrooms contain biologically active polysaccharides which are important for modern medicine [22]. Aqueous extracts contained high proportion of water-soluble constituents such as polysaccharides, such as β-glucan and water soluble components. Studies showed that aqueous extraction was employed to extract water-soluble polysaccharide from edible medicinal mushrooms. However, bioactive compounds from medicinal plants extracted with ethanol performed better activities than aqueous extractions [23] but aqueous extraction is believed to have lower cytotoxicity effect than ethanol extraction [24].

Wong et al. reported that freeze drying may be the best method for long-term preservation of bioactive compounds in mushroom responsible for neurite outgrowth stimulation activity. Inactivation of bioactive compound via oxidation could cause short cellular outgrowth of neurite and insufficient elongation to be scored as neurite [9]. Lower concentrations of aqueous extract may contain less active compounds and therefore insufficient for neuron to sense and instruct neuronal elongation process. Higher concentrations of extract could have toxic effect and eventually cause nerve cell damage. Based on the data collected, sclerotium of L. rhinocerus displayed NGF-like properties due to obvious morphological alteration shown by PC-12 cells. Further work on fractionation of L. rhinocerus extract that possesses NGF-like properties needs to be explored.

NGF is a signaling molecule that plays an important role in the differentiation and survival of peripheral sensory and sympathetic neurons [25]. When PC-12 cells were treated with NGF, G1 phase of Interphase was blocked and differentiation was initiated [26]. PC-12 experienced a dramatic phenotypic change when treated with NGF [10]. Percentage of neurite bearing cells of NGF-treated cells at optimum concentration of NGF increased as much as five times compared to non-NGF-treated cells. NGF activates extracellular signal-regulated kinase (ERK)—mitogen-activated protein (MAP) kinase pathway is responsible of neurotrophic responses in PC-12 cells [27].

Neurite outgrowth takes place in neuron (in vivo and in vitro differentiation). When neurosecretory cells, a type of neuron, were exposed to neurotrophins, peptides, and adhesion proteins, such as glycoproteins [28, 29], the activity took several hours to few days to perform differentiation [28]. Two major growth factor receptor downstream cascades involved in cell survival and neurite outgrowth are the phosphatidylinositol-3-kinase-Akt (PI3K-Akt) pathway and Ras-mitogen-activated protein kinase (Ras-MAPK) pathway. PI3K-Akt is vital in mediating neurotrophin-promoted cell survival whereas Ras-MAPK may be involved in mediating neurite-outgrowth [30]. Atwal et al. study showed that activation of TrkB-Shc site mediates neuronal survival and axonal outgrowth via PI3K-Akt and Ras-MAPK pathway [31]. EGF and NGF are a potent activator of ERK1/2 pathway in PC-12 cell line [31] and sustained activation of NGF is crucial for neurite outgrowth [32]. Lignosus rhinocerus extract that possessed NGF-like properties may be responsible for the activation able to activate Akt which is required in combination with activated MAPK cascade proteins for neurite outgrowth.

Neurofilament protein acts as a major component of the axonal cytoskeleton and was synthesized and assembled for axonal transport in cell body. After axon has grown and connected to its target cell, diameter of axon may increase as much as fivefold. Therefore, neurofilament proteins increased during NGF-induced PC-12 differentiation [32] and also conferring some degree of cellular protection rather than causing rapid cell death during cell death mechanism [33]. Besides that, morphological alteration cells observation under microscope, indirect immunofluorescence technique is an alternative to assess neuronal differentiation by neuronal marker on PC-12 cell line.

Additive effect occurs when there is a combination of two or more drugs with same therapeutic effect and the result is the sum of the drug’s effects [34]. NGF action was enhanced by the aqueous extract at concentrations of 10, 20, 30, and 40 μg/mL (w/v) whereas showed a weaker activity at combination with 50 μg/mL (w/v). Combination of aqueous extract and NGF neurite showed outgrowth activity.

Researchers found that some compounds extracted from mushrooms, for instance, tricholomalides from Tricholoma sp. [35], termitomycesphins from Termitomyces albuminosus [36], and dictyoquinazol and dictyophorines from Dictyophora indusiata [37, 38], were active toward neurons. Lysophosphatidylethanolamine from Grifola frondosa was found to induce activation of MAP kinase cascade in PC-12 cells and resulted in neuronal differentiation and suppression of serum deprivation-induced apoptosis [39]. Tremella fuciformis crude aqueous extract contains polysaccharides, including glycosaminoglycan, promoted neuritogenesis, peripheral nerve regeneration, and muscle reinnervation following a sciatic nerve lesion [40–42]. Park et al. reported that exo-polysaccharides from the culture broth of Hericium erinaceus were shown to enhance the growth and neuronal differentiation of rat pheochromocytoma cells (PC-12) [43]. Nonpolar compounds of H. erinaceus known as erinacines extracted from mycelium have been well investigated and proven as strong stimulators of NGF [44, 45]. It promotes NGF gene expression via JNK signaling by inducing phosphorylation of JNK and its downstream substrate c-Jun and increased c-fos expression [46].

Water extracts of the rhizome of a traditional herb, Coptis chinensis, induced the growth of axon and dendrite and showed a sustained neurite outgrowth for a longer period whereas NGF-induced neurite did not maintain a fully differentiated state after 14 days in culture [47]. The nonpolar fraction of an Ayurvedic herb, Centella asiatica, known as asiatic acid showed significant neurite outgrowth activity on human SH-SY5Y cells [48].

Our results indicated that aqueous extract of L. rhinocerus contained compound/s that have potent NGF-addtive effect. It will be important to discover the compounds in L. rhinocerus that stimulate neurite outgrowth activity. As this mushroom is currently being investigated to validate traditional uses, the chemistry is not well known. Aqueous extracts are said to certain high molecular weight polysaccharides that have anti-inflammatory properties [49]. To our knowledge, this is the first report on neurite outgrowth activity of L. rhinocerus. With further development and investigation, L. rhinocerus and its bioactive compounds may be developed as mushroom nutraceutical to enhance process of neurite outgrowth activity in an aging population of humans.

Further detailed investigations are needed to ascertain clinical use of the extract in treating any neurodegenerative diseases and bioactive compounds that are responsible for neurite outgrowth activity have to be elucidated. This mushroom has been used as traditional medicine by indigenous folks of Malaysia for more than 15 diseases. The ethnopharmacological knowledge has to be scientifically validated to enable use of this mushroom as a nutraceutical or pharmaceutical. The findings warrant further studies of L. rhinocerus not only for nerve regeneration but also as a therapeutic agent for neurodegenerative diseases.

4. Conclusion

Aqueous extract of L. rhinocerus sclerotium contained NGF-like compound/s that enhanced neurite outgrowth activity. There was an enhanced stimulation of 17% of neurite outgrowth when a combination of 20 μg/mL (w/v) aqueous extract and 30 ng/mL (w/v) NGF was added to PC-12 compared to the aqueous extract alone.

Funding

This work was supported by grants from the University of Malaya RG 136/10AFR, PS311/2010B, TA021-2010, 66-02-03-0074, and F000002-21001.

Acknowledgments

The authors would like to thank Dr. Tan Chon Seng (MARDI) and Ligno Biotech Sdn. Bhd. for mushroom samples. The helpful suggestions on statistical analysis by Dr. Khang Tsung Fei of the University of Malaya are greatly appreciated.

References

N. Díez-Revuelta, S. Velasco, S. André et al., “Phosphorylation of adhesion- and growth-regulatory human galectin-3 leads to the induction of axonal branching by local membrane L1 and ERM redistribution,” Journal of Cell Science, vol. 123, no. 5, pp. 671–681, 2010.
View at: Publisher Site | Google Scholar
P. J. Mitchell, J. C. Hanson, A. T. Quets-Nguyen, M. Bergeron, and R. C. Smith, “A quantitative method for analysis of in vitro neurite outgrowth,” Journal of Neuroscience Methods, vol. 164, no. 2, pp. 350–362, 2007.
View at: Publisher Site | Google Scholar
P. K. Parmar, L. C. Coates, J. F. Pearson, R. M. Hill, and N. P. Birch, “Neuroserpin regulates neurite outgrowth in nerve growth factor-treated PC12 cells,” Journal of Neurochemistry, vol. 82, no. 6, pp. 1406–1415, 2002.
View at: Publisher Site | Google Scholar
Y. Kim, R. Seger, C. V. Suresh Babu, S. Y. Hwang, and Y. S. Yoo, “A positive role of the PI3-K/Akt signaling pathway in PC12 cell differentiation,” Molecules and Cells, vol. 18, no. 3, pp. 353–359, 2004.
View at: Google Scholar
“The Fire within,” The Sun, 2011.
View at: Google Scholar
C.S. Tan, “Lignosus rhinocerus (Cooke) Ryvarden 1972,” Encyclopedia of Life, 2009, http://www.eol.org/pages/192772.
View at: Google Scholar
C. S. Tan, S. T. Ng, S. Vikineswary, F. P. Lo, and C. S. Tee, “Genetic markers for identification of a Malaysian medicinal mushroom, Lignosus rhinocerus (Cendawan Susu Rimau),” Acta Horticulturae, vol. 859, pp. 161–168, 2010.
View at: Google Scholar
S. Vikineswary, A. Noorlidah, I. Normah, Y. H. Tan, D. Fauzi, and E. B. G. Jones, “Edible and medicinal mushrooms,” in Malaysian Fungal Diversity, E. B. G. Jones, K. D. Hyde, and S. Vikineswary, Eds., pp. 287–305, Mushroom Research Centre, University of Malaysia and Ministry of National Resources and Environment, Kuala Lumpur, Malaysia, 2007.
View at: Google Scholar
K. H. Wong, S. Vikineswary, N. Abdullah, M. Naidu, and R. Keynes, “Activity of aqueous extracts of lion's mane mushroom Hericium erinaceus (Bull.: Fr.) Pers. (Aphyllophoromycetideae) on the neural cell line NG108-15,” International Journal of Medicinal Mushrooms, vol. 9, no. 1, pp. 57–65, 2007.
View at: Publisher Site | Google Scholar
K. Ohnuma, Y. Hayashi, M. Furue, K. Kaneko, and M. Asashima, “Serum-free culture conditions for serial subculture of undifferentiated PC12 cells,” Journal of Neuroscience Methods, vol. 151, no. 2, pp. 250–261, 2006.
View at: Publisher Site | Google Scholar
K. P. Das, T. M. Freudenrich, and W. R. Mundy, “Assessment of PC12 cell differentiation and neurite growth: a comparison of morphological and neurochemical measures,” Neurotoxicology and Teratology, vol. 26, no. 3, pp. 397–406, 2004.
View at: Publisher Site | Google Scholar
N. R. Smalheiser and N. B. Schwartz, “Kinectic analysis of “rapid onset“ neurite formation in NG108-15 cells reveals a dual role for substratum-bound laminin,” Developmental Brain Research, vol. 34, no. 1, pp. 111–121, 1987.
View at: Google Scholar
“American type culture collection. Product information sheet for ATCC CRL-1721.1TM,” 2011, http://www.atcc.org.
View at: Google Scholar
A. Murphy, K. C. Breen, A. Long, C. Feighery, E. B. Casey, and D. Kelleher, “Neurofilament expression in human T lymphocytes,” Immunology, vol. 79, no. 1, pp. 167–170, 1993.
View at: Google Scholar
P. Good, Permutation Tests: A Practical Guide to Resampling Methods for Testing Hypotheses, Springer, New York, NY, USA, 2nd edition, 2000.
J. B. Du Prel, G. Hommel, B. Röhrig, and M. Blettner, “Confidence interval or p-value? Part 4 of a series on evaluation of scientific publications,” Deutsches Arzteblatt, vol. 106, no. 19, pp. 335–339, 2009.
View at: Publisher Site | Google Scholar
T. P. Shakespeare, V. J. Gebski, M. J. Veness, and J. Simes, “Improving interpretation of clinical studies by use of confidence levels, clinical significance curves, and risk-benefit contours,” Lancet, vol. 357, no. 9265, pp. 1349–1353, 2001.
View at: Publisher Site | Google Scholar
J. Schimmelpfeng, K. F. Weibezahn, and H. Dertinger, “Quantification of NGF-dependent neuronal differentiation of PC-12 cells by means of neurofilament-L mRNA expression and neuronal outgrowth,” Journal of Neuroscience Methods, vol. 139, no. 2, pp. 299–306, 2004.
View at: Publisher Site | Google Scholar
T. Tojima, Y. Yamane, M. Takahashi, and E. Ito, “Acquisition of neuronal proteins during differentiation of NG108-15 cells,” Neuroscience Research, vol. 37, no. 2, pp. 153–161, 2000.
View at: Publisher Site | Google Scholar
A. Matus, “Neurofilament protein phosphorylation—where, when and why,” Trends in Neurosciences, vol. 11, no. 7, pp. 291–292, 1988.
View at: Google Scholar
E. Nwachukwu and H. O. Uzoeto, “Antimicrobial activity of some local mushrooms on pathogenic isolates,” Journal of Medicinal Plant Research, vol. 4, no. 23, pp. 2460–2465, 2010.
View at: Google Scholar
S. Wasser, “Medicinal mushrooms as a source of antitumor and immunomodulating polysaccharides,” Applied Microbiology and Biotechnology, vol. 60, no. 3, pp. 258–274, 2002.
View at: Publisher Site | Google Scholar
V. I. Obi and C. Onuoha, “Extraction and characterization methods of plants and plant products,” in Biological and Agricultural Techniques, pp. 271–286, Websmedia publishers, Owerri, Nigeria, 2nd edition, 2000.
View at: Google Scholar
R. M. Faridur, K. M. Rezaul, I. M. Farhadul, H. M. Rowshanul, and H. M. Tofazzal, “Phytochemical and cytotoxic investigation on oyester mushroom (Pleurotus ostreatus),” International Research Journal of Pharmacy, vol. 1, no. 1, pp. 342–345, 2010.
View at: Google Scholar
M. Fiore, G. N. Chaldakov, and L. Aloe, “Nerve growth factor as a signaling molecule for nerve cells and also for the neuroendocrine-immune systems,” Reviews in the Neurosciences, vol. 20, no. 2, pp. 133–145, 2009.
View at: Google Scholar
L. A. Van Grunsven, N. Billon, P. Savatier, A. Thomas, J. L. Urdiales, and B. B. Rudkin, “Effect of nerve growth factor on the expression of cell cycle regulatory proteins in PC12 cells: dissection of the neurotrophic response from the anti-mitogenic response,” Oncogene, vol. 12, no. 6, pp. 1347–1356, 1996.
View at: Google Scholar
J. Xing, J. M. Kornhauser, Z. Xia, E. A. Thiele, and M. E. Greenberg, “New growth factor activates extracellular signal-regulated kinase and p38 mitogen-activated protein kinase pathways to stimulate CREB serine 133 phosphorylation,” Molecular and Cellular Biology, vol. 18, no. 4, pp. 1946–1955, 1998.
View at: Google Scholar
G. Racchetti, A. Lorusso, C. Schulte et al., “Rapid neurite outgrowth in neurosecretory cells and neurons is sustained by the exocytosis of a cytoplasmic organelle, the enlargeosome,” Journal of Cell Science, vol. 123, no. 2, pp. 165–170, 2010.
View at: Publisher Site | Google Scholar
A. Ravni, S. Bourgault, A. Lebon et al., “The neurotrophic effects of PACAP in PC12 cells: control by multiple transduction pathways,” Journal of Neurochemistry, vol. 98, no. 2, pp. 321–329, 2006.
View at: Publisher Site | Google Scholar
M. Naidu, R. P. David, R. Asher, and J. Fawcett, “Expression of akt and MAPK in the normal and regenerating peripheral nerves and their dorsal root ganglia,” Malaysian Journal of Biochemistry and Molecular Biology, vol. 17, no. 1, pp. 16–19, 2009.
View at: Google Scholar
J. K. Atwal, B. Massie, F. D. Miller, and D. R. Kaplan, “The TrkB-Shc site signals neuronal survival and local axon growth via MEK and PI3-Kinase,” Neuron, vol. 27, no. 2, pp. 265–277, 2000.
View at: Google Scholar
T. Ohuchi, S. Maruoka, A. Sakudo, and T. Arai, “Assay-based quantitative analysis of PC12 cell differentiation,” Journal of Neuroscience Methods, vol. 118, no. 1, pp. 1–8, 2002.
View at: Publisher Site | Google Scholar
C. E. Shepherd, H. McCann, E. Thiel, and G. M. Halliday, “Neurofilament-immunoreactive neurons in Alzheimer's disease and dementia with Lewy bodies,” Neurobiology of Disease, vol. 9, no. 2, pp. 249–257, 2002.
View at: Publisher Site | Google Scholar
D. S. Aschenbrenner and S. J. Venable, Drug Therapy in Nursing, Lippincott Williams & Wilkins, Philadelphia, Pa, USA, 3rd edition, 2008.
S. Tsukamoto, A. D. Macabalang, K. Nakatani, Y. Obara, N. Nakahata, and T. Ohta, “Tricholomalides A-C, new neurotrophic diterpenes from the mushroom Tricholoma sp,” Journal of Natural Products, vol. 66, no. 12, pp. 1578–1581, 2003.
View at: Publisher Site | Google Scholar
J. Qi, M. Ojika, and Y. Sakagami, “Termitomycesphins A-D, novel neuritogenic cerebrosides from the edible Chinese mushroom Termitomyces albuminosus,” Tetrahedron, vol. 56, no. 32, pp. 5835–5841, 2000.
View at: Google Scholar
I. K. Lee, B. S. Yun, G. Han, D. H. Cho, Y. H. Kim, and I. D. Yoo, “Dictyoquinazols A, B, and C, new neuroprotective compounds from the mushroom Dictyophora indusiata,” Journal of Natural Products, vol. 65, no. 12, pp. 1769–1772, 2002.
View at: Publisher Site | Google Scholar
H. Kawagishi, D. Ishiyama, H. Mori et al., “Dictyophorines A and B, two stimulators of NGF-synthesis from the mushroom Dictyophora indusiata,” Phytochemistry, vol. 45, no. 6, pp. 1203–1205, 1997.
View at: Publisher Site | Google Scholar
A. Nishina, H. Kimura, A. Sekiguchi, R. H. Fukumoto, S. Nakajima, and S. Furukawa, “Lysophosphatidylethanolamine in Grifola frondosa as a neurotrophic activator via activation of MAPK,” Journal of Lipid Research, vol. 47, no. 7, pp. 1434–1443, 2006.
View at: Publisher Site | Google Scholar
J. H. Kim, H. C. Ha, M. S. Lee et al., “Effect of Tremella fuciformis on the neurite outgrowth of PC12h cells and the improvement of memory in rats,” Biological and Pharmaceutical Bulletin, vol. 30, no. 4, pp. 708–714, 2007.
View at: Publisher Site | Google Scholar
A. Gorio, E. Lesma, L. Vergani, and A. M. Di Giulio, “Glycosaminoglycan supplementation promotes nerve regeneration and muscle reinnervation,” European Journal of Neuroscience, vol. 9, no. 8, pp. 1748–1753, 1997.
View at: Publisher Site | Google Scholar
E. Lesma, A. M. Di Giulio, L. Ferro, G. Prino, and A. Gorio, “Glycosaminoglycans in nerve injury: I. Low doses of glycosaminoglycans promote neurite formation,” Journal of Neuroscience Research, vol. 46, no. 5, pp. 565–571, 1996.
View at: Publisher Site | Google Scholar
Y. S. Park, H. S. Lee, M. H. Won, J. H. Lee, S. Y. Lee, and H. Y. Lee, “Effect of an exo-polysaccharide from the culture broth of Hericium erinaceus on enhancement of growth and differentiation of rat adrenal nerve cells,” Cytotechnology, vol. 39, no. 3, pp. 155–162, 2002.
View at: Publisher Site | Google Scholar
H. Kawagishi, A. Shimada, S. Hosokawa et al., “Erinacines E, F, and G, stimulators of nerve growth factor (NGF)-synthesis, from the mycelia of Hericium erinaceum,” Tetrahedron Letters, vol. 37, no. 41, pp. 7399–7402, 1996.
View at: Publisher Site | Google Scholar
E. W. Lee, K. Shizuki, S. Hosokawa et al., “Two novel diterpenoids, erinacines H and I from the mycelia of Hericium erinaceum,” Bioscience, Biotechnology and Biochemistry, vol. 64, no. 11, pp. 2402–2405, 2000.
View at: Google Scholar
K. Mori, Y. Obara, M. Hirota et al., “Nerve growth factor-inducing activity of Hericium erinaceus in 1321N1 human astrocytoma cells,” Biological and Pharmaceutical Bulletin, vol. 31, no. 9, pp. 1727–1732, 2008.
View at: Publisher Site | Google Scholar
G. Y. Kwon, B. K. Choe, and S. K. Kim, “Neurotropic and neuritogenic effects of water extracts of rhizoma of Coptis chinensis Franch in PC12 cells,” Korean Journal of Physiology and Pharmacology, vol. 7, no. 3, pp. 175–179, 2003.
View at: Google Scholar
A. Soumyanath, Y. P. Zhong, S. A. Gold et al., “Centella asiatica accelerates nerve regeneration upon oral administration and contains multiple active fractions increasing neurite elongation in-vitro,” Journal of Pharmacy and Pharmacology, vol. 57, no. 9, pp. 1221–1229, 2005.
View at: Publisher Site | Google Scholar
N. H. Tan, “Biopharmacological studies of tiger's milk mushroom “cendawan susu rimau“ (Lignosus rhinocerus),” in Proceedings of the Academia Sinica-University of Malaya International Workshop on Molecular Medicine & Biotechnology, University of Malaya, Kuala Lumpur, Malaysia, 2011.
View at: Google Scholar

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Copyright © 2012 Lee-Fang Eik et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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