Distribution of osteonectin mRNA and protein during human embryonic and fetal developmentS Mundlos, B Schwahn, T Reichert and B Zabel Department of Pediatrics, Johannes-Gutenberg-University Mainz, Federal Republic of Germany. We investigated the temporal and spatial distribution of osteonectin during human embryonic and fetal development, using in situ hybridization and immunohistochemistry. Osteonectin gene expression was generally found in cells exhibiting high rates of matrix production/proliferation. In mineralized tissue, a strong signal was obtained in osteoblasts, odontoblasts, and chondrocytes of the upper hypertrophic and proliferative zones. Chondrocytes of the mineralized zone showed no expression throughout the different stages of development. Strong osteonectin expression was found in odontoblasts of developing teeth. In addition, osteonectin mRNA and protein were detected in several non-mineralized tissues: steroid-producing cells of the adrenal gland and the gonads, kidney (glomeruli), lung (bronchi), skin, megacaryocytes, and large vessels. Histochemistry confirmed the results and detected extracellular osteonectin in bone and in the zone of mineralized cartilage only. The localization of osteonectin in bone, cartilage, and teeth is consistent with a role in the initiation of mineralization. However, the organ-specific distribution in non- mineralized tissues suggests an important multifunction role of this protein during human development.
Volume 40,
Issue 2,
pp. 283-291,
02/01/1992
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H. Ishimoto, D. G. Ginzinger, T. Matsumoto, Y. Hattori, M. Furuya, K. Minegishi, M. Tanaka, Y. Yoshimura, and R. B. Jaffe Differential Zonal Expression and Adrenocorticotropin Regulation of Secreted Protein Acidic and Rich in Cysteine (SPARC), a Matricellular Protein, in the Midgestation Human Fetal Adrenal Gland: Implications for Adrenal Development J. Clin. Endocrinol. Metab., August 1, 2006; 91(8): 3208 - 3214. [Abstract] [Full Text] [PDF] |
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J. T. Hecht and E. H. Sage Retention of the Matricellular Protein SPARC in the Endoplasmic Reticulum of Chondrocytes from Patients with Pseudoachondroplasia J. Histochem. Cytochem., March 1, 2006; 54(3): 269 - 274. [Abstract] [Full Text] [PDF] |
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L. Rodriguez, Z. Cheng, T.-H. Chen, C. Tu, and W. Chang Extracellular Calcium and Parathyroid Hormone-Related Peptide Signaling Modulate the Pace of Growth Plate Chondrocyte Differentiation Endocrinology, November 1, 2005; 146(11): 4597 - 4608. [Abstract] [Full Text] [PDF] |
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A. Chlenski, S. Liu, S. E. Crawford, O. V. Volpert, G. H. DeVries, A. Evangelista, Q. Yang, H. R. Salwen, R. Farrer, J. Bray, et al. SPARC Is a Key Schwannian-derived Inhibitor Controlling Neuroblastoma Tumor Angiogenesis Cancer Res., December 15, 2002; 62(24): 7357 - 7363. [Abstract] [Full Text] [PDF] |
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C. Schultz, N. Lemke, S. Ge, W. A. Golembieski, and S. A. Rempel Secreted Protein Acidic and Rich in Cysteine Promotes Glioma Invasion and Delays Tumor Growth in Vivo Cancer Res., November 1, 2002; 62(21): 6270 - 6277. [Abstract] [Full Text] [PDF] |
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W. Chang, C. Tu, S. Pratt, T.-H. Chen, and D. Shoback Extracellular Ca2+-Sensing Receptors Modulate Matrix Production and Mineralization in Chondrogenic RCJ3.1C5.18 Cells Endocrinology, April 1, 2002; 143(4): 1467 - 1474. [Abstract] [Full Text] [PDF] |
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M. COZZOLINO, A. S. DUSSO, and E. SLATOPOLSKY Role of Calcium-Phosphate Product and Bone-Associated Proteins on Vascular Calcification in Renal Failure J. Am. Soc. Nephrol., November 1, 2001; 12(11): 2511 - 2516. [Full Text] [PDF] |
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G. K. Yiu, W. Y. Chan, S.-W. Ng, P. S. Chan, K. K. Cheung, R. S. Berkowitz, and S. C. Mok SPARC (Secreted Protein Acidic and Rich in Cysteine) Induces Apoptosis in Ovarian Cancer Cells Am. J. Pathol., August 1, 2001; 159(2): 609 - 622. [Abstract] [Full Text] |
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P.C. McParland, S.C. Bell, J.H. Pringle, and D.J. Taylor Regional and cellular localization of osteonectin/SPARC expression in connective tissue and cytotrophoblastic layers of human fetal membranes at term Mol. Hum. Reprod., May 1, 2001; 7(5): 463 - 474. [Abstract] [Full Text] [PDF] |
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A.-P. Gadeau, H. Chaulet, D. Daret, M. Kockx, J.-M. Daniel-Lamazière, and C. Desgranges Time Course of Osteopontin, Osteocalcin, and Osteonectin Accumulation and Calcification After Acute Vessel Wall Injury J. Histochem. Cytochem., January 1, 2001; 49(1): 79 - 86. [Abstract] [Full Text] |
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S. A. Rempel, S. Ge, and J. A. Gutierrez SPARC: A Potential Diagnostic Marker of Invasive Meningiomas Clin. Cancer Res., February 1, 1999; 5(2): 237 - 241. [Abstract] [Full Text] [PDF] |
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G. L. Evans, E. Morey-Holton, and R. T. Turner Spaceflight has compartment- and gene-specific effects on mRNA levels for bone matrix proteins in rat femur J Appl Physiol, June 1, 1998; 84(6): 2132 - 2137. [Abstract] [Full Text] [PDF] |
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Q. Yan, E. H. Sage, and A. E. Hendrickson SPARC Is Expressed by Ganglion Cells and Astrocytes in Bovine Retina J. Histochem. Cytochem., January 1, 1998; 46(1): 3 - 10. [Abstract] [Full Text] |
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J. A. Soderling, M. J. Reed, A. Corsa, and E. H. Sage Cloning and Expression of Murine SC1, a Gene Product Homologous to SPARC J. Histochem. Cytochem., June 1, 1997; 45(6): 823 - 836. [Abstract] [Full Text] [PDF] |
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P J McKinnon, M Kapsetaki, and R F Margolskee The exon structure of the mouse Sc1 gene is very similar to the mouse Sparc gene. Genome Res., November 1, 1996; 6(11): 1077 - 1083. [Abstract] [PDF] |
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A Poleev, H Fickenscher, S Mundlos, A Winterpacht, B Zabel, A Fidler, P Gruss, and D Plachov PAX8, a human paired box gene: isolation and expression in developing thyroid, kidney and Wilms' tumors Development, January 11, 1992; 116(3): 611 - 623. [Abstract] [PDF] |
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