Skip to main content
Erschienen in: Medical Molecular Morphology 4/2016

28.04.2016 | Original Paper

Alterations of collagen-producing cells in human pituitary adenomas

verfasst von: Alimuddin Tofrizal, Ken Fujiwara, Takashi Yashiro, Shozo Yamada

Erschienen in: Medical Molecular Morphology | Ausgabe 4/2016

Einloggen, um Zugang zu erhalten

Abstract

Extracellular matrix (ECM) is essential in tissue physiology and pathologic conditions such as tumorigenesis. ECM affects tumor cell behavior, proliferation, and metastasis. Pituitary adenomas vary in their clinical characteristics, including ECM deposition. However, the mechanism of desmoplasia in pituitary adenoma is not well understood. The present study focused on the principal component of ECM, collagen, and attempted to characterize collagen-producing cells in pituitary adenomas. Specimens of human pituitary adenomas and control pituitary were obtained during surgery. In situ hybridization for collagen I and III and immunohistochemistry for α-smooth muscle actin (a pericyte marker) and cytokeratin (an epithelial cell marker) were performed. The results showed that pericytes were the sole collagen-producing cells in control pituitary, while four types of collagen-producing cells were present in pituitary adenomas: pericytes, myofibroblasts, fibroblasts, and newly characterized “myoepithelial-like cells”. Azan staining showed that fibrous matrix deposition varied among pituitary adenomas and that the area of fibrosis was associated with the number and types of collagen-producing cells. These results suggest that changes in the number and type of collagen-producing cells influence ECM arrangement, which may in turn reflect pathologic characteristics in pituitary adenomas.
Literatur
1.
Zurück zum Zitat Evans JJ, Chitcholtan K (2011) Extracellular matrix proteins in the anterior pituitary gland. Open Neuroendocr J 4:111–119CrossRef Evans JJ, Chitcholtan K (2011) Extracellular matrix proteins in the anterior pituitary gland. Open Neuroendocr J 4:111–119CrossRef
2.
Zurück zum Zitat McNicol AM (2000) Tumors of the pituitary gland. In: Fletcher CDM (ed) Diagnostic histopathology of tumors. Churchill Livingstone, New York, pp 691–703 McNicol AM (2000) Tumors of the pituitary gland. In: Fletcher CDM (ed) Diagnostic histopathology of tumors. Churchill Livingstone, New York, pp 691–703
3.
Zurück zum Zitat SojiT Herbert DC (1989) Intercellular communication between rat anterior pituitary cells. Anat Rec 224:523–533CrossRef SojiT Herbert DC (1989) Intercellular communication between rat anterior pituitary cells. Anat Rec 224:523–533CrossRef
4.
Zurück zum Zitat Fujiwara K, Jindatip D, Kikuchi M, Yashiro T (2010) In situ hybridization reveals that type I and III collagens are produced by pericytes in the anterior pituitary gland of rats. Cell Tissue Res 342:491–495CrossRefPubMed Fujiwara K, Jindatip D, Kikuchi M, Yashiro T (2010) In situ hybridization reveals that type I and III collagens are produced by pericytes in the anterior pituitary gland of rats. Cell Tissue Res 342:491–495CrossRefPubMed
5.
Zurück zum Zitat Fujiwara K, Davaadash B, Yatabe M, Kikuchi M, Horiguchi K, Kusumoto K, Kouki T, Yashiro T (2008) Reduction of retinaldehyde dehydrogenase 1 expression and production in estrogen-induced prolactinoma of rat. Med Mol Morphol 41:126–131CrossRefPubMed Fujiwara K, Davaadash B, Yatabe M, Kikuchi M, Horiguchi K, Kusumoto K, Kouki T, Yashiro T (2008) Reduction of retinaldehyde dehydrogenase 1 expression and production in estrogen-induced prolactinoma of rat. Med Mol Morphol 41:126–131CrossRefPubMed
6.
Zurück zum Zitat Vannucci L (2015) Stroma as an active player in the development of the tumor microenvironment. Cancer Microenviron 8:159–166CrossRefPubMed Vannucci L (2015) Stroma as an active player in the development of the tumor microenvironment. Cancer Microenviron 8:159–166CrossRefPubMed
7.
Zurück zum Zitat Paez-Pereda M, Kuchenbauer F, Arzt E, Stalla GK (2005) Regulation of pituitary hormones and cell proliferation by components of the extracellular matrix. Braz J Med Biol Res 38:1487–1494CrossRefPubMed Paez-Pereda M, Kuchenbauer F, Arzt E, Stalla GK (2005) Regulation of pituitary hormones and cell proliferation by components of the extracellular matrix. Braz J Med Biol Res 38:1487–1494CrossRefPubMed
8.
Zurück zum Zitat Yamada S, Fukuhara N, Horiguchi K, Yamaguchi-Okada M, Nishioka H, Takeshita A, Takeuchi Y, Ito J, Inoshita N (2014) Clinicopathological characteristics and therapeutic outcomes in thyrotropin-secreting pituitary adenomas: a single-center study of 90 cases. J Neurosurg 121:1462–1473CrossRefPubMed Yamada S, Fukuhara N, Horiguchi K, Yamaguchi-Okada M, Nishioka H, Takeshita A, Takeuchi Y, Ito J, Inoshita N (2014) Clinicopathological characteristics and therapeutic outcomes in thyrotropin-secreting pituitary adenomas: a single-center study of 90 cases. J Neurosurg 121:1462–1473CrossRefPubMed
9.
Zurück zum Zitat Jarzembowski J, Lloyd R, McKeever P (2007) Type IV collagen immunostaining is a simple, reliable diagnostic tool for distinguishing between adenomatous and normal pituitary glands. Arch Pathol Lab Med 131:931–935PubMed Jarzembowski J, Lloyd R, McKeever P (2007) Type IV collagen immunostaining is a simple, reliable diagnostic tool for distinguishing between adenomatous and normal pituitary glands. Arch Pathol Lab Med 131:931–935PubMed
10.
Zurück zum Zitat Wang H, Li WS, Shi DJ, Ye ZP, Tai F, He HY, Liang CF, Gong J, Guo Y (2008) Correlation of MMP(1) and TIMP(1) expression with pituitary adenoma fibrosis. J Neurooncol 90:151–156CrossRefPubMed Wang H, Li WS, Shi DJ, Ye ZP, Tai F, He HY, Liang CF, Gong J, Guo Y (2008) Correlation of MMP(1) and TIMP(1) expression with pituitary adenoma fibrosis. J Neurooncol 90:151–156CrossRefPubMed
11.
Zurück zum Zitat Gudjonsson T, Ronnov-Jessen L, Villadsen R, Rank F, Bissell MJ, Petersen OW (2002) Normal and tumor-derived myoepithelial cells differ in their ability to interact with luminal breast epithelial cells for polarity and basement membrane deposition. J Cell Sci 115:39–50PubMedPubMedCentral Gudjonsson T, Ronnov-Jessen L, Villadsen R, Rank F, Bissell MJ, Petersen OW (2002) Normal and tumor-derived myoepithelial cells differ in their ability to interact with luminal breast epithelial cells for polarity and basement membrane deposition. J Cell Sci 115:39–50PubMedPubMedCentral
12.
Zurück zum Zitat Chen WL, Huang CH, Chiou LL, Chen TH, Huang YY, Jiang CC, Lee HS, Dong CY (2010) Multiphoton imaging and quantitative analysis of collagen production by chondrogenic human mesenchymal stem cells cultured in chitosan scaffold. Tissue Eng 16:913–920CrossRef Chen WL, Huang CH, Chiou LL, Chen TH, Huang YY, Jiang CC, Lee HS, Dong CY (2010) Multiphoton imaging and quantitative analysis of collagen production by chondrogenic human mesenchymal stem cells cultured in chitosan scaffold. Tissue Eng 16:913–920CrossRef
13.
Zurück zum Zitat Lin SL, Kisseleva T, Brenner DA, Duffield JS (2008) Pericytes and perivascular fibroblasts are the primary source of collagen producing cells in obstructive fibrosis of the kidney. Am J Pathol 173:1617–1627CrossRefPubMedPubMedCentral Lin SL, Kisseleva T, Brenner DA, Duffield JS (2008) Pericytes and perivascular fibroblasts are the primary source of collagen producing cells in obstructive fibrosis of the kidney. Am J Pathol 173:1617–1627CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Sundberg C, Ivarsson M, Gerdin B, Rubin K (1996) Pericytes as collagen-producing cells in excessive dermal scarring. Lab Invest 74:452–466PubMed Sundberg C, Ivarsson M, Gerdin B, Rubin K (1996) Pericytes as collagen-producing cells in excessive dermal scarring. Lab Invest 74:452–466PubMed
16.
Zurück zum Zitat Hinz B, Phan SH, Thannickal VJ, Galli A, Bochaton-Piallat ML, Gabbiani G (2007) The myofibroblast. One function multiple origins. Am J Pathol 170:1807–1816CrossRefPubMedPubMedCentral Hinz B, Phan SH, Thannickal VJ, Galli A, Bochaton-Piallat ML, Gabbiani G (2007) The myofibroblast. One function multiple origins. Am J Pathol 170:1807–1816CrossRefPubMedPubMedCentral
17.
Zurück zum Zitat McAnulty RJ (2007) Fibroblasts and myofibroblasts: their source, function and role in disease. Int J Biochem Cell Biol 39:666–671CrossRefPubMed McAnulty RJ (2007) Fibroblasts and myofibroblasts: their source, function and role in disease. Int J Biochem Cell Biol 39:666–671CrossRefPubMed
18.
Zurück zum Zitat Kato T, Mizuno S, Ito A (2014) A decrease in glomerular endothelial cells and endothelial-mesenchymal transition during glomerulosclerosis in the Tensin2-deficient mice (ICGN strain). Acta Histochem Cytochem 47:265–271CrossRefPubMedPubMedCentral Kato T, Mizuno S, Ito A (2014) A decrease in glomerular endothelial cells and endothelial-mesenchymal transition during glomerulosclerosis in the Tensin2-deficient mice (ICGN strain). Acta Histochem Cytochem 47:265–271CrossRefPubMedPubMedCentral
19.
Zurück zum Zitat Gudjonsson T, Adriance MC, Sternlicht MD, Petersen OW, Bissell MJ (2005) Myoepithelial cells: their origin and function in breast morphogenesis and neoplasia. J Mammary Gland Biol Neoplasia 10:261–272CrossRefPubMedPubMedCentral Gudjonsson T, Adriance MC, Sternlicht MD, Petersen OW, Bissell MJ (2005) Myoepithelial cells: their origin and function in breast morphogenesis and neoplasia. J Mammary Gland Biol Neoplasia 10:261–272CrossRefPubMedPubMedCentral
20.
Zurück zum Zitat Nagao T, Sato E, Inoue R, Oshiro H, Takahashi RH, Nagai T, Yoshida M, Suzuki F, Obikane H, Yamashina M, Matsubayashi J (2012) Immunohistochemical analysis of salivary gland tumors: application for surgical pathology practice. Acta Histochem Cytochem 45:269–282CrossRefPubMedPubMedCentral Nagao T, Sato E, Inoue R, Oshiro H, Takahashi RH, Nagai T, Yoshida M, Suzuki F, Obikane H, Yamashina M, Matsubayashi J (2012) Immunohistochemical analysis of salivary gland tumors: application for surgical pathology practice. Acta Histochem Cytochem 45:269–282CrossRefPubMedPubMedCentral
21.
22.
Zurück zum Zitat DiTommaso L, Pasquinelli G, Damiani S (2003) Smooth muscle cell differentiation in mammary stromo-epithelial lesions with evidence of a dual origin: stromal myofibroblasts and myoepithelial cells. Histopathology 42:448–456CrossRef DiTommaso L, Pasquinelli G, Damiani S (2003) Smooth muscle cell differentiation in mammary stromo-epithelial lesions with evidence of a dual origin: stromal myofibroblasts and myoepithelial cells. Histopathology 42:448–456CrossRef
24.
Zurück zum Zitat Abbass SAA, Asa SL, Ezzat S (1997) Altered expression of fibroblast growth factor receptors in human pituitary adenomas. J Clin Endocrinol Metab 82:1160–1166CrossRefPubMed Abbass SAA, Asa SL, Ezzat S (1997) Altered expression of fibroblast growth factor receptors in human pituitary adenomas. J Clin Endocrinol Metab 82:1160–1166CrossRefPubMed
25.
Zurück zum Zitat Ren P, Scheithauer BW, Halper J (1994) Immunohistological localization of TGF alpha, EGF, IGF-I and TGF beta in the normal human pituitary gland. Endocr Pathol 5:40–48CrossRef Ren P, Scheithauer BW, Halper J (1994) Immunohistological localization of TGF alpha, EGF, IGF-I and TGF beta in the normal human pituitary gland. Endocr Pathol 5:40–48CrossRef
26.
Zurück zum Zitat Visse R, Nagase H (2003) Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure, function, and biochemistry. Circ Res 92:827–839CrossRefPubMed Visse R, Nagase H (2003) Matrix metalloproteinases and tissue inhibitors of metalloproteinases: structure, function, and biochemistry. Circ Res 92:827–839CrossRefPubMed
27.
Zurück zum Zitat Tomita T (1997) Matrix metalloproteinases and tissue inhibitors of metalloproteinases in pituitary adenomas: possible markers of neuroendocrine cells. Endocr Pathol 8:305–313CrossRefPubMed Tomita T (1997) Matrix metalloproteinases and tissue inhibitors of metalloproteinases in pituitary adenomas: possible markers of neuroendocrine cells. Endocr Pathol 8:305–313CrossRefPubMed
Metadaten
Titel
Alterations of collagen-producing cells in human pituitary adenomas
verfasst von
Alimuddin Tofrizal
Ken Fujiwara
Takashi Yashiro
Shozo Yamada
Publikationsdatum
28.04.2016
Verlag
Springer Japan
Erschienen in
Medical Molecular Morphology / Ausgabe 4/2016
Print ISSN: 1860-1480
Elektronische ISSN: 1860-1499
DOI
https://doi.org/10.1007/s00795-016-0140-9

Weitere Artikel der Ausgabe 4/2016

Medical Molecular Morphology 4/2016 Zur Ausgabe

Neu im Fachgebiet Pathologie