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10.1007/s00418-015-1319-1

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suck abstract from ncbi


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pmid25850409      Histochem+Cell+Biol 2015 ; 144 (1): 1-11
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  • Identification of receptor-type protein tyrosine phosphatase ? as a new marker for osteocytes #MMPMID25850409
  • de Rooij KE; van der Velde M; de Wilt E; Deckers MML; Bezemer M; Waarsing JH; Que I; Chan AB; Kaijzel EL; Löwik CWGM
  • Histochem Cell Biol 2015[]; 144 (1): 1-11 PMID25850409show ga
  • Osteocytes are the predominant cells in bone, where they form a cellular network and display important functions in bone homeostasis, phosphate metabolism and mechanical transduction. Several proteins strongly expressed by osteocytes are involved in these processes, e.g., sclerostin, DMP-1, PHEX, FGF23 and MEPE, while others are upregulated during differentiation of osteoblasts into osteocytes, e.g., osteocalcin and E11. The receptor-type protein tyrosine phosphatase µ (RPTP?) has been described to be expressed in cells which display a cellular network, e.g., endothelial and neuronal cells, and is implied in mechanotransduction. In a capillary outgrowth assay using metatarsals derived from RPTP?-knock-out/LacZ knock-in mice, we observed that the capillary structures grown out of the metatarsals were stained blue, as expected. Surprisingly, cells within the metatarsal bone tissue were positive for LacZ activity as well, indicating that RPTP? is also expressed by osteocytes. Subsequent histochemical analysis showed that within bone, RPTP? is expressed exclusively in early-stage osteocytes. Analysis of bone marrow cell cultures revealed that osteocytes are present in the nodules and an enzymatic assay enabled the quantification of the amount of osteocytes. No apparent bone phenotype was observed when tibiae of RPTP?-knock-out/LacZ knock-in mice were analyzed by ?CT at several time points during aging, although a significant reduction in cortical bone was observed in RPTP?-knock-out/LacZ knock-in mice at 20 weeks. Changes in trabecular bone were more subtle. Our data show that RPTP? is a new marker for osteocytes.
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