Cathepsin K (CTSK) is a member of the papain-like cysteine protease family. Mutations in the CTSK gene cause a rare autosomal recessive bone disorder called pycnodysostosis (OMIM 265800). In order to follow the advances in the research about CTSK and pycnodysostosis, we performed a literature retrospective study of 159 pycnodysostosis patients reported since 1996 and focused on the genetic characteristics of CTSK mutations and/or the clinical phenotypes of pycnodysostosis. Thirty three different CTSK mutations have been found in 59 unrelated pycnodysostosis families. Of the 59 families, 37.29% are from Europe and 30.51% are from Asia. A total of 69.70% of the mutations were identified in the mature domain of CTSK, 24.24% in the proregion, and 6.06% in the preregion. The hot mutation spots are found in exons 6 and 7. CTSK mutations result in total loss or inactivity of the CTSK protein, which causes abnormal degradation of bone matrix proteins such as type I collagen. Skeletal abnormalities, including short stature, an increase in bone density with pathologic fractures, and open fontanels and sutures, are the typical phenotypes of pycnodysostosis. Research on Ctsk-/- mouse models was also reviewed here to elucidate the biological function of Ctsk and the mechanism of pycnodysostosis. New evidence suggests that Ctsk plays an important role in the immune system and may serve as a valid therapeutic target in the future treatment of pycnodysostosis.
The online version of this article (doi:10.1186/1750-1172-6-20) contains supplementary material, which is available to authorized users.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
YX participated in reviewing papers and drafted the manuscript. TC participated in its design and helped to modify the manuscript. SS participated in its design and helped to modify the manuscript. WW participated in reviewing papers and analyzing data. YZ participated in finding papers and analyzing data. TM conceived of the study, and participated in its design and coordination and helped to modify the manuscript. XD conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
Abkürzungen
COS-7 cells
COS-7 SV40-transformed kidney cells
CTSK
Ctsk: cathepsin K
Hb
hemoglobin
IL-6
interleukin 6
IL-23
interleukin 23
MCV
mean corpuscular volume
RANKL
receptor activator of nuclear factor kappa B ligand
Th17
T helper 17 cells
Introduction
Pycnodysostosis (OMIM 265800) is a rare autosomal recessive bone disorder resulting from osteoclast dysfunction [1‐4]. The first case of pycnodysostosis was described in 1923 by Montanari; however, Maroteaux and Lamy defined the typical features of pycnodysostosis (Greek: pycnos = dense; dys = defective; osteon = bone) in 1962. Thus, it is also known as Maroteaux-Lamy syndrome. This disorder is also called Toulouse-Lautrec syndrome after the famous French artist Henri de Toulouse-Lautrec, who was thought to be afflicted with the disease [2, 3, 5]. Less than 200 cases have been reported worldwide since 1962 [1]. The prevalence of pycnodysostosis is estimated to be 1 to 1.7 per million with equal sex distribution [4‐7]. The typical features of pycnodysostosis include short stature, an increase in the bone density of long bones, pathological fractures with poor healing, stubby hands and feet with dystrophic nails, unossified fontanels, and an obtuse mandibular angle [5, 8‐10].
The candidate gene for pycnodysostosis was mapped to human chromosome 1q21 by genetic linkage analysis, and was subsequently identified as coding for cathepsin K (CTSK, MIM# 601105) by a positional cloning strategy in 1996 [11‐13]. The CTSK gene spans approximately 12 kb (GenBank acc. no., NC_000001.10) and contains 8 exons (GenBank acc. no., NM_000396.2). The codon for the translation initiator methionine (Met1) is located in exon 2, whereas the termination codon is located in exon 8. The CTSK protein, highly similar to cathepsins S and L, is a member of the papain-like cysteine protease family. Like most papain-like cysteine proteases, CTSK consists of 329 amino acids (GenBank acc. no., NP_000387.1), including a 15-amino acid preregion, a 99-amino acid proregion, and a 215-amino acid mature active enzyme [14]. CTSK is synthesized as an inactive precursor protein and requires removal of its N-terminal proregion for activation. This autocatalytic process occurs under a low-pH environment [3].
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To date, it is difficult to find a full description of the characteristics of specific gene mutations and clinical manifestations of pycnodysostosis in the literature. In this study, we analyzed the reported CTSK mutations and summarized the typical clinical features of pycnodysostosis from 159 reported patients and some animal research findings in Ctsk gene knockout mice (Ctsk-/-mice). Early reports of CTSK mutations were renamed in this study with the first base in the CTSK gene (GenBank acc. no., NC_000001.10) as the +1 position in genomic DNA, and the A of the ATG-translation initiation codon as nucleotide +1 in cDNA (GenBank acc. no., NM_000396.2).
Structure of CTSK
CTSK is also called lysosomal cysteine cathepsin K because it contains a cysteine in its active site and functions mainly in lysosomes [15]. Like most lysosomal cysteine proteases, CTSK is synthesized as an inactive proenzyme [3, 16]. The preregion plays a critical role in targeting the protein to the endoplasmic reticulum and translocating the protein across the membrane [17‐19]. While the proregion plays a role in protein folding and intracellular trafficking, it can also inhibit protease function until the proenzyme reaches the lysosome [20]. The proregion contains a conserved N-glycosylation site (Asn103), which is supposed to facilitate lysosomal trafficking via the mannose 6-phosphate receptor pathway [11, 14, 20]. The proenzyme requires removal of its N-terminal proregion for activation [16]. This process has been proven to be autocatalytic in lysosomes at a pH of 4 [3, 21]. CTSK consists of 2 domains folded together, resulting in a V-shaped configuration [22, 23]. The catalytic triad, consisting of Cys139, His276, and Asn296 in the active sites, localizes at the bottom of the V cleft [14, 15, 24, 25].
Distribution of CTSK
CTSK is highly expressed in osteoclasts and has lower expression levels in the heart, lung, skeletal muscle, colon, ovary, and placenta [3, 5, 20]. Additionally, CTSK mRNA was detected in macrophages and bone marrow-derived dendritic cells, but was barely detected in nonadherent bone marrow cells or splenic T cells [26, 27].
Function of CTSK
In osteoclasts
CTSK, which is critical for osteoclast-mediated bone resorption, is highly expressed in osteoclasts. In osteoclasts, CTSK is responsible for the degradation of bone matrix proteins, such as type I collagen, osteopontin, and osteonectin [3, 5, 20]. A tightly sealed resorption lacuna between the osteoclast and the bone is called an extracellular lysosome. Dissolution of the inorganic matrix and degradation of the organic matrix occur in the extracellular lysosome under low pH conditions [28, 29]. In mature osteoclasts, CTSK is synthesized as an inactive proenzyme and cleaved by autoproteolysis to produce the active form of the protein. This active form is then secreted into the extracellular lysosome [30‐32], where it degrades bone matrix proteins, particularly type I collagen, which constitutes 95% of the organic bone matrix [3, 5, 15, 20, 33]. CTSK deficiency does not affect the function of osteoclast-mediated extracellular acidification [34]. Ctsk mutations were found to impair the ability of osteoclasts to degrade collagen rather than demineralize the extracellular matrix.
On the other hand, CTSK may also act as a potential regulator of apoptosis and senescence, controlling osteoclast numbers in vivo[34]. Thus, impairment of CTSK-mediated osteoclast apoptosis/senescence may also be responsible for the higher number of osteoclasts found in Ctsk-/-mice [34].
In immunocytes
A pycnodysostosis patient with normal immune status was reported in 1999 [35]. However, impaired killing activity of monocytes with normal phagocytic capacity and decreased levels of IL-1 secretion were reported in pycnodysostosis patients in an earlier study [36].
In an early animal study, abnormities of histological morphology or cellularity were found neither in the thymus nor in the levels of B and T lymphocytes in peripheral blood [37]. Fluorescence-activated cell sorter analysis showed no difference in the lymphocyte markers (CD4, CD8, CD3, B220, IgM, and IgD) between Ctsk-/- and wild-type mice. Immunophenotype analysis of the cell types in the bone marrow revealed a significant decrease in the absolute cell number of all subtypes, even though the percentage of each subtype in the entire population was unchanged [37].
Recently, Ctsk was found to function in the endosomes of dendritic cells. Pharmacological inhibition or targeted disruption of Ctsk led to defective Toll-like receptor 9 signaling in dendritic cells when stimulated with cytosine-phosphate- guanine, but not when stimulated with lipopolysaccharide or peptidoglycan. It was shown that Ctsk is indispensable for differentiation of dendritic cells, but not required for antigen uptake, processing, or presentation by dendritic cells. The same study also indicated that the ability of dendritic cells to induce T helper 17 (Th17) cells was markedly inhibited by Ctsk inactivation, which may be caused by a reduction in the expression of Th17 cell-related cytokines, such as IL-6 and IL-23, by dendritic cells. Furthermore, Ctsk-/-mice were resistant to experimental autoimmune encephalomyelitis, in which Th17 cells are involved [26]. These results suggest that Ctsk plays an important role in the immune system and may serve as a valid therapeutic target in autoimmune diseases.
Nevertheless, it remains to be determined whether CTSK plays a pathogenic role in the human immune system or in autoimmune/inflammatory diseases.
In other cells and tissues
New evidence suggests that CTSK is involved in extracellular matrix remodeling in organs such as the lung, thyroid, and skin, and plays a critical role in the development and progression of cardiovascular disease [38]. Extensive destruction of elastin and collagen caused by overexpression of cathepsins K and S has been related to the damage and inflammation of arterial wall, resulting in atherogenesis [15, 38‐41].
Variants in the CTSK gene
Thirty three different mutations have been reported in 59 pycnodysostosis families [1, 3, 8, 9, 14, 17, 20, 42‐54] (Table 1, Figure 1A). The Arg241 in exon 6 and Ala277 located in CpG dinucleotides in exon 7 are two mutational hot spots for pycnodysostosis (Figure 1B). Various mutations have been reported in pycnodysostosis patients, including 23 missense mutations (69.70%), 4 frame-shift mutations (12.12%), 3 nonsense mutations (9.09%), 2 splicing mutations (6.06%), and 1 termination codon mutation (3.03%) (Figure 1C). A total of 69.70% of the mutations occur in the mature domain of CTSK, 24.24% in the proregion, and 6.06% in the preregion (Figure 1D).
Table 1
Mutations in the CTSK gene causing pycnodysostosis
Location in DNA sequence
Genomic DNA sequence variants
Coding DNA sequence variants
Effect on amino acid
Location in protein sequence
First description
Missense
Exon 2
g.1551T > C
c.20T > C
p.Leu7Pro
Pre
Donnarumma, et al., 2007
Exon 2
g.1557T > C
c.26T > C
p.Leu9Pro
Pre
Nishi, et al., 1999
Exon 3
g.2128C > T
c.136C > T
p.Arg46Trp
Pro
Schilling, et al., 2007
Exon 3
g.2227G > A
c.235G > A
p.Gly79Arg
Pro
Fratzl-Zelman, et al., 2004
Exon 3
g.2228G > A
c.236G > A
p.Gly79Glu
Pro
Hou, et al., 1999
Exon 5
g.4120C > T
c.422C > T
p.Ala141Val
Mature
Chavassieux, et al., 2008
Exon 5
g.4134G > C
c.436G > C
p.Gly146Arg
Mature
Gelb, et al., 1996
Exon 5
g.4192A > G
c.494A > G
p.Gln165Arg
Mature
Donnarumma, et al., 2007
Exon 5
g.4258A > C
c.560A > C
p.Gln187Pro
Mature
Li, et al., 2009
Exon 5
g.4278G > A
c.580G > A
p.Gly194Ser
Mature
Donnarumma, et al., 2007
Exon 6
g.8644A > G
c.635A > G
p.Tyr212Cys
Mature
Hou, et al., 1999
Exon 6
g.8737 G > A
c.728G > A
p.Gly243Glu
Mature
Khan et al., 2010
Exon 6
g.8755T > C
c.746T > C
p.Ile249Thr
Mature
Donnarumma, et al., 2007
Exon 6
g.8758A > G
c.749A > G
p.Asp250Gly
Mature
Donnarumma, et al., 2007
Exon 7
g.9109C > T
c.830C > T
p.Ala277Val
Mature
Gelb, et al., 1998
Exon 7
g.9109C > A
c.830C > A
p.Ala277Glu
Mature
Hou, et al., 1999
Exon 7
g.9171T > C
c.892T > C
p.Trp298Arg
Mature
Nishi, et al., 1999
Exon 8
g.9186G > A
c.908G > A
p.Gly303Glu
Mature
Toral-Lopez et al., 2010
Exon 8
g.11474T > C
c.926T > C
p.Leu309Pro
Mature
Haagerup, et al., 2000
Exon 8
g.11479G > C
c.931G > C
p.Ala311Pro
Mature
Nishi, et al., 1999
Exon 8
g.11482C > G
c.934C > G
p.Arg312Gly
Mature
Hou, et al., 1999
Exon 8
g.11501G > A
c.953G > A
p.Cys318Tyr
Mature
Bertola et al., 2010
Exon 8
g.11503G > T
c.955G > T
p.Gly319Cys
Mature
Donnarumma, et al., 2007
Nonsense
Exon 3
g.2146A > T
c.154A > T
p.Lys52X
Pro
Hou, et al., 1999
Exon 5
g.4266C > T
c.568C > T
p.Gln190X
Mature
Hou, et al., 1999
Exon 6
g.8730C > T
c.721C > T
p.Arg241X
Mature
Gelb, et al., 1996
Frameshifts (duplication)
Exon 2
g.1591-1592dupGA
c.60_61dupGA
p.Ile21ArgfsX29
Pro
Donnarumma, et al., 2007
Exon 4
g.2359dupA
c.282dupA
p.Val95SerfsX9
Pro
Donnarumma, et al., 2007
Frameshifts (deletion)
Exon 3
g.2230delG
c.238delG
p.Asp80ThrfsX2
Pro
Fratzl-Zelman, et al., 2004
Exon 5
g.4124delT
c.426delT
p.Phe142LeufsX19
Mature
Fujita, et al., 2000
Splicing
Intron2
g.2112G > A
c.121-1G > A
p.del41Val-81Met
Pro
Haagerup, et al., 2000
Exon 7
g.9169G > A
c.890G > A; 785_890del
p.Gly262AlafsX70
Mature
Donnarumma, et al., 2007
Stop codon
Exon 8
g.11538A > G
c.990A > G
p.X330TrpextX19
Mature
Gelb, et al., 1996
Figure 1
Reported mutations ofCTSK. (A) Distribution of the CTSK gene and polypeptide mutations. The genomic structure of the CTSK gene with 8 exons (purple boxes numbered 1-8) is shown in the top half. The bottom half illustrates the schematic representation of the polypeptide comprising a 15-amino acid preregion (yellow box), a 99-residue proregion (light blue boxes), and a 215-amino acid mature domain (orange boxes). A total of 23 missense mutations (black type) are represented at the top of the gene diagram, while frame-shift mutations (red type), nonsense mutations (light green type), splicing mutations (blue type), and termination codon mutations (yellow type) are at the bottom. (B) Frequency of different mutations. The height of each bar represents the number of afflicted families. #: Both mutations in the Glu70 residue. ##: Both mutations in the Ala277 residue. (C) The type of reported CTSK mutations. The mutations reported in pycnodysostosis patients consist of 23 missense mutations, 4 frame-shift mutations, 3 nonsense mutations, 2 splicing mutations, and 1 termination codon mutation. (D) Distribution of reported CTSK mutations. A total of 69.70% of the mutations occurred in the mature domain, 24.24% in the proregion, and 6.06% in the preregion.
×
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The reported families and characteristics of different mutations are summarized in Table 2. In addition to paternal uniparental disomy in 1 family, compound heterozygous mutations were found in 14 afflicted families (23.73%), while homozygous mutations were found in 44 afflicted families (74.58%). Of the 59 unrelated families, 37.29% were from Europe while 30.51% came from Asia.
Table 2
Genotypes of pycnodysostosis patients from different nationalities
Allele 1
Allele 2
Patients reported
Unrelated families
Nationality of patients
Reference
c.436G > C
c.436G > C
1
1
Algerian
Osimani, et al., 2009
c.436G > C
c.721C > T
1
1
American Hispanic
Gelb, et al., 1996
c.235G > A
c.238delG
1
1
Austria
Fratzl-Zelman, et al., 2004
c.934C > G
c.934C > G
1
1
Austria
Fratzl-Zelman, et al., 2004
c.830C > T
c.830C > T
1
1
Belgian
Gelb, et al., 1998
c.953G > A
c.953G > A
2
2
Brazil
Bertola et al., 2010
c.953G > A
c.721C > T
1
1
Brazil
Bertola et al., 2010
c.721C > T
c.436G > C
1
1
Brazil
Bertola et al., 2010
c.721C > T
c.721C > T
2
2
Brazil
Bertola et al., 2010
c.494A > G
c.721C > T
1
1
Caucasian
Laffranchi et al., 2010
c.154A > T
c.236G > A
2
1
Caucasian
Ho, et al., 1999
c.560A > C
c.560A > C
1
1
Chinese
Li, et al., 2009
c.121-1G > A
c.926T > C
1
1
Denmark
Haagerup, et al., 2000
c.236G > A
c.926T > C
1
1
Denmark
Haagerup, et al., 2000
c.926T > C
c.926T > C
6
3
Denmark
Haagerup, et al., 2000
c.890G > A; 785_890del
c.890G > A; 785_890del
1
1
Egypt
Donnarumma, et al., 2007
c.136C > T
c.136C > T
3
1
Germany
Schilling, et al., 2007
c.934C > G
c.934C > G
2
1
Honduran
Hou, et al., 1999
c.830C > A
c.830C > A
1
1
Indian
Hou, et al., 1999
c.990A > G
c.990A > G
16
1
Israeli Arab
Gelb, et al., 1996
c.20T > C
c.580G > A
1
1
Italy
Donnarumma, et al., 2007
c.494A > G
c.721C > T
1
1
Italy
Donnarumma, et al., 2007
c.26T > C
c.26T > C
2
2
Japanese
Nishi, et al., 1999; Fujita, et al., 2000
c.26T > C
c.892T > C
1
1
Japanese
Nishi, et al., 1999
c.426delT
c.426delT
2
2
Japanese
Fujita, et al., 2000
c.830C > T
c.830C > T
3
3
Japanese
Nishi, et al., 1999; Fujita, et al., 2000
c.721C > T
c.721C > T
10
1
Mexican
Johnson, et al., 1996
c.908G > A
c.908G > A
3
1
Mexican
Toral-Lopez et al., 2010
c.60_61dupGA
c.60_61dupGA
3
1
Moroccan
Donnarumma, et al., 2007
c.436G > C
c.436G > C
1
1
Moroccan
Rothenbuhler et al., 2010
c.436G > C
c.436G > C
2
1
Moroccan Arab
Gelb, et al., 1996
c.282dupA
c.282dupA
1
1
Pakistan
Donnarumma, et al., 2007
c.728G > A
c.728G > A
5
1
Pakistani
Khan et al., 2010
c.749A > G
c.749A > G
1
1
Pakistan
Donnarumma, et al., 2007
c.830C > T
c.830C > T
5
3
Pakistan
Donnarumma, et al., 2007; Naeem, et al., 2009
c.955G > T
c.955G > T
1
1
Pakistan
Donnarumma, et al., 2007
c.721C > T
c.721C > T
2
2
Portuguese
Hou, et al., 1999; Donnarumma, et al., 2007
c.830C > A
c.830C > A
1
1
Portuguese
Hou, et al., 1999
c.635A > G
c.721C > T
1
1
Spanish
Hou, et al., 1999
c.721C > T
c.746T > C
1
1
Spanish
Donnarumma, et al., 2007
c.721C > T
c.721C > T
1
1
Spanish
Rothenbuhler et al., 2010
c.931G > C
c.931G > C
2
1
Swiss
Nishi, et al., 1999
c.436G > C
c.436G > C
1
1
Tunisia
Donnarumma, et al., 2007
c.154A > T
c.236G > A
1
1
*
Hou, et al., 1999
c.568C > T
c.568C > T
1
1
*
Hou, et al., 1999
c.830C > T
c.830C > T
1
1
*
Hou, et al., 1999
c.422C > T
c.422C > T
1
1
Unknown
Chavassieux, et al., 2008
c.721C > T
c.721C > T
3
1
Unknown
Everts, et al., 2003
*: Two of the three families are from northern Europe, while the other is from Czech (no detailed record can be found in corresponding papers).
Characteristics of mutant CTSK proteins
In order to determine CTSK expression, monocyte-derived macrophages were isolated from the peripheral blood of 2 siblings suffering from pycnodysostosis and their unaffected parents. Western blot revealed no detectable expression of either the proform or mature form of CTSK in either affected sibling with p.Gly79Glu and p.Lys52X. The levels of both proform and mature forms of CTSK in the father, a carrier of p.Gly79Glu, were nearly half that in normal controls, while the levels in the mother, a carrier of p.Lys52X, were more severely decreased [50]. In another study, monocytes were isolated from the peripheral blood of a patient with p.Ala141Val and induced to differentiate into osteoclasts in vitro. As a result of the mutation, the ability of the patient-derived cells to resorb bone was significantly decreased [46].
Functional properties of CTSK mutants (p.Leu7Pro, p.Leu9Pro, p.Gly79Glu, p.Gly146Arg, p.Gln165Arg, p.Gly194Ser, p.Tyr212Cys, p.Ile249Thr, p.Asp250Gly, p.Ala277Glu, p.Ala277Val, p.Arg312Gly, p.Gly319Cys, and p.X330Trp) were examined by transient expression in COS-7 cells, 293 cells, and Pichia pastoris GS115 cells, respectively [14, 17, 20, 54]. Western blot analysis revealed that the mutants affecting residues of the mature domain yielded a mature form of a nonfunctional protein, while the mutants p.Leu7Pro, p.Leu9Pro, and p.X330Trp yielded a trace amount of this protein. In order to further understand the protein consequences of these missense mutations, amino acid changes of the mutant proteins, including p.Leu7Pro, p.Leu9Pro, p.Gln165Arg, p.Gly194Ser, p.Ile249Thr, p.Asp250Gly, and p.Gly319Cys, were modeled into the three-dimensional structure of the full-length CTSK. These mutations are predicted to affect the conformation of the protein [14].
All of these methods, including isolation of monocytes from the pycnodysostosis patients and transfection in COS-7 cells, 293 cells, and P. pastoris GS115 cells, demonstrated that CTSK mutants are functionally different from the wild type.
Ctsk-/- mouse models
The murine Ctsk gene maps to chromosome 3, and its predicted amino acid sequence is highly homologous to the human protein (85% identity; 93% similarity) [11]. Ctsk-/- mouse models play quite an important role in studying the nature and function of Ctsk in osteoclasts and other cells, in detecting the mechanisms of phenotypes of pycnodysostosis, and even in optimizing therapeutic strategies (including gene therapy) for the treatment of this genetic disorder [34, 55]. A homozygous null mutation in the mouse Ctsk gene was first established in 1998. Ctsk-/- mouse strains have been generated in different genetic backgrounds since then [34, 37, 56‐58]. All Ctsk-/- mouse strains could mimic the phenotype of human pycnodysostosis to different extents.
Generally, Ctsk deficient mice may survive and are fertile. The phenotype of Ctsk-/-mice resembles clinical characteristics of the human pycnodysostosis in several aspects, such as the presence of osteopetrosis, reduced bone marrow cellularity, and splenomegaly after 2 months of age [37, 58]. Using radiography, micro-computed tomography, and histological analyses, Ctsk-/- mice were shown to display an osteopetrotic phenotype with excessive trabeculation of the bone marrow space [56]. Deficiency of Ctsk affects the late stage of the osteoclastic resorption cycle. As a result, Ctsk-/- mice are unique among the currently available osteopetrotic mouse models [56].
Ctsk-/- mice generally have minor craniofacial anomalies, such as increased density of the maxilla and paranasal sinus bones as well as alterations in mandibular shape [37]. Other skeletal changes seen in pycnodysostosis patient, such as growth retardation, phalangeal deformities, and delayed suture closure in the skull, have seldom been reported in Ctsk-/- mice. Recent studies found that the pycnodysostosis phenotype in Ctsk-/- mice is background-dependent. Compared with other strains of Ctsk-/-mice, the phenotypical characteristics of 129/Sv Ctsk-/-mice were similar to those of human pycnodysostosis, including short stature, osteopetrosis in the long bones, spondylolysis, acroosteolysis, bone fragility, separated cranial sutures with open fontanels, loss of the mandibular angle, lack of normal occlusion, and enhanced open bite [34].
A transgenic mouse model overexpressing the Ctsk gene showed that excess Ctsk production resulted in a high turnover of the metaphyseal trabecular bone. Enhanced bone resorption in these mice led to increased osteoblast numbers and activities, possibly mediated by core-binding protein α1, a transcription factor essential for osteoblast differentiation [56].
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Clinical relevance
A series of typical features in clinical and radiological examinations have been observed in pycnodysostosis. We summarized the manifestations in 97 reported cases (Table 3) [1‐10, 17, 35, 42‐47, 50, 52, 53, 59‐91]. The most common phenotype of pycnodysostosis is short stature, which was reported in 95.9% of the 97 reported cases. The next most common phenotype is an increase in bone density, which was reported in 88.7% of the 97 patients. Open fontanels and sutures with frontal and parietal bossing, frequent fractures, hypoplasia of the maxilla and mandible with an obtuse mandibular angle, and stubby hands and feet with acroosteolysis of the distal phalanges were identified in more than 50% of the pycnodysostosis patients. Approximately one-third of the pycnodysostosis patients showed prominent eyes with bluish sclera. Additionally, these patients also show some dental defects, such as delayed eruption of permanent teeth with persistence of deciduous teeth, dental crowding, and malocclusion, which may be ignored by clinicians.
Table 3
Typical clinical features of pycnodysostosis*
Typical features
Positive
Negative
Not mentioned
Short stature (<150 cm)
93(95.9%)
0
4(4.1%)
Increase of bone density
86(88.7%)
0
11(11.3%)
Open fontanels and sutures
68-73(70.1%-75.3%)
0
24-29(24.7%-29.9%)
Frontal and parietal bossing
67-72(69.1%-74.2%)
0
25-30(25.8%-30.9%)
Fractures
65(67.0%)
3(3.1%)
29(29.9%)
Obtuse mandibular angle
63(64.9%)
0
34(35.1%)
Hypoplasia of the jaws
53-61(54.6%-62.9%)
0
36-44(37.1%-45.4%)
Stubby hands and feet with osteolysis of the distal phalanges
43-50(44.3%-51.5%)
0
47-54(48.5%-55.7%)
Prominent eyes with bluish sclerae
34(35.1%)
0
63(64.9%)
Grooved palate
20-28(20.6%-28.9%)
0
69-77(71.1%-79.4%)
Dysplastic nails
26(26.8%)
0
71(73.2%)
Clavicular dysplasia
24(24.7%)
0
73(75.3%)
Nonpneumatised paranasal sinuses
17(17.5%)
0
80(82.5%)
Beaked nose
16(16.5%)
0
81(83.5%)
*n = 97 (44 females, 42 males, and 11 unknown)
In addition to the typical manifestations mentioned above, some unusual findings, including hearing loss [5], central giant-cell granuloma of the maxilla [82], congenital pseudarthrosis of the clavicle [7], spondylolysis [79], and bone marrow hypoplasia with compensatory splenomegaly [76], were reported in pycnodysostosis patients.
Pycnodysostosis patients usually have normal life expectancies and mentations. Results of laboratory investigations, including leukocyte and thrombocyte number; mean corpuscular volume (MCV); and the levels of hemoglobin (Hb), plasma phosphate, calcium, and alkaline phosphatase, are usually within normal limits [1, 3‐5].
Physiopathological mechanism of pycnodysostosis
Abnormal bone metabolism is the typical physiopathological characterics of pycnodysostosis. The most common phenotype of pycnodysostosis is short stature. Based on the results of animal experiments, the short stature in pycnodysostosis may be related to the reduced size of the long bones [37].
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In addition, pycnodysostosis patients usually suffer from pathologic fractures as a result of brittle, chalk-like bones. Histomorphometric and biomechanical assays in Ctsk-/- mice have suggested that CTSK may play a critical role in matrix formation as well as breakdown. Large amounts of brittle, poorly organized matrix were formed in the absence of Ctsk gene, which corresponds to the bone fragility observed in patients with CTSK deficiency [57].
The coexistence of increased bone density in long bones (osteosclerosis) and osteolysis in the distal phalanges and calvariae is a typical characteristic of pycnodysostosis with CTSK mutation. One explanation may be the site-specific variations in bone homeostasis. It was reported that CTSK is clearly important to bone resorption in rapidly remodeling bones (e.g., the long bones), while it is not the most essential factor in regulating the bone resorption in bones with low turnover rates, such as the calvaria and epiphysis [34, 37, 48]. On the other hand, animal experiments have shown that metalloproteinases participate in osteoclastic resorption of calvarial bones, but not of long bones [34]. The increased number of Ctsk-/- osteoclasts may result in excessive bone resorption in the distal end of long bones (osteolysis), and the impaired ability of osteoclasts may account for the osteopetrosis in the main body of long bones [34, 37, 48, 56].
Immunophenotype analysis of the cell types in the bone marrow of Ctsk-/- mice revealed reductions in absolute cell numbers, but not in the percentages of all the different subtypes, indicating that marrow hypoplasia results from the reduction in bone marrow cavity space, which is caused by osteopetrosis. As a result, extramedullary hematopoiesis occurs in the spleen (enlarged with a significantly elevated cellularity) to compensate for the reduced bone marrow cellularity [37].
Diagnosis and differential diagnoses
Although CTSK gene mutation analysis is the confirmatory test for pycnodysostosis, the diagnosis can be established primarily based on the aforementioned clinical features and radiograph findings [5]. On the other hand, pycnodysostosis should be distinguished from other genetic bone diseases, particularly cleidocranial dysostosis (CCD) and osteopetrosis [5, 47, 68]. Clavicular hypoplasia and typical craniofacial characteristics, especially the open fontanels and cranial sutures in pycnodysostosis, may lead to misdiagnosis of cleidocranial dysplasia. However, increased bone density with recurrent fractures is highly suggestive of pycnodysostosis [92‐95]. Short stature and generalized osteosclerosis with multiple fractures in pycnodysostosis patients has been misdiagnosed as osteopetrosis [71, 96‐98]. However, acroosteolysis of the distal phalanges and unclosed cranial sutures and fontanels are indicative of pycnodysostosis.
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Treatment
To date, no specific treatment has been validated in pycnodysostosis with the exception of symptomatic management [5, 46]. Because bone fractures are a primary threat to these patients, it is important to prevent fracture-causing factors. These patients are likely to visit dentists because oral deformities severely affect their life. Here, we would like to emphasize the role of dentists in the diagnosis and treatment of this condition. Maintenance of oral hygiene and regular dental care may help prevent some oral complications. However, the greater bone density increases the probability of developing postextraction osteomyelitis. Thus, risk factors should be carefully addressed while planning tooth extraction and other treatments. In summary, it is quite important to establish a correct diagnosis as early as possible to prevent fractures and ensure a better quality of life [5, 6, 54].
Future prospects
Genotype-phenotype correlation draws great attention in the field of genetic disorder research. Clinical features with CTSK genetic analysis were reported in 42 pycnodysostosis patients from 24 families [1, 3, 8, 9, 17, 42‐47, 50, 52, 53]. However, the detailed clinical information was poorly described in most of the reports with molecular data. Lack of good clinical information makes it difficult to evaluate of the genotype-phenotype correlation of pycnodysostosis. More detailed information about the clinical and genetic characteristics in pycnodysostosis patients are necessary for the further research to elucidate the CTSK genotype-phenotype correlation.
Research on specific approaches to correct the abnormal bone metabolism in pycnodysostosis is another hot topic. Due to providing normal osteoclasts and osteoclast-targeted enzymes, bone marrow transplantation is drawing the increasing attention. Gene replacement strategies are other alternative choices. However, considerable research is required in this area [54].
Recently, CTSK was shown to play an important role in autoimmune and inflammatory diseases by animal and in vitro experiments [26]. If the role of CTSK in the human immune system is confirmed [99], it will be helpful in further understanding of the mechanism of pycnodysostosis and in designing specific treatment strategies.
Acknowledgements and Funding
This work was supported in part by grants of Key Projects of Science and Technology of Xi'an City of China [SF09027(4)], Key Projects of Science and Technology of Shaanxi Province of China (2009K17-06), and National Scientific Foundation of China (81070819). As a disclaimer, T.C. represented his own perspective in the paper, not the NIDCR/NIH.
Open Access
This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License (
https://creativecommons.org/licenses/by/2.0
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
YX participated in reviewing papers and drafted the manuscript. TC participated in its design and helped to modify the manuscript. SS participated in its design and helped to modify the manuscript. WW participated in reviewing papers and analyzing data. YZ participated in finding papers and analyzing data. TM conceived of the study, and participated in its design and coordination and helped to modify the manuscript. XD conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
