Literature DB >> 29091523

Osteogenic Potential of Caspases Related to Endochondral Ossification.

Eva Janečková1,2, Petra Bíliková1, Eva Matalová1,3.   

Abstract

Caspases have functions particularly in apoptosis and inflammation. Increasing evidence indicates novel roles of these proteases in cell differentiation, including those involved in osteogenesis. This investigation provides a complex screening of osteogenic markers affected by pan caspase inhibition in micromass cultures derived from mouse forelimbs. PCR Array analysis showed significant alterations in expression of 49 osteogenic genes after 7 days of inhibition. The largest change was a decrease in CD36 expression, which was confirmed at organ level by caspase inhibition in cultured mouse ulnae followed by CD36 immunohistochemical analysis. So far, available data point to osteogenic potential of pro-apoptotic caspases. Therefore, the expression of pro-apoptotic caspases (-3, -6, -7, -8, -9) within the growth plate of mouse forelimbs at the stage where the individual zones are clearly apparent was studied. Caspase-9 was reported in the growth plate for the first time as well as caspase-6 and -7 in the resting zone, caspase-7 in the proliferation, and caspase-6 and -8 in the ossification zone. For all caspases, there was a gradient increase in activation toward the ossification zone. The distribution of staining varied significantly from that of apoptotic cells, and thus, the results further support non-apoptotic participation of caspases in osteogenesis.

Entities:  

Keywords:  PCR Array analysis; caspases; endochondral ossification; growth plate; immunohistochemistry; micromass cultures

Mesh:

Substances:

Year:  2017        PMID: 29091523      PMCID: PMC5761947          DOI: 10.1369/0022155417739283

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  58 in total

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3.  Caspase inhibition supports proper gene expression in ex vivo mouse limb cultures.

Authors:  D De Valck; F P Luyten
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Journal:  J Cell Physiol       Date:  2006-12       Impact factor: 6.384

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Authors:  Thomas Q Nhan; W Conrad Liles; Stephen M Schwartz
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7.  High density micromass cultures of embryonic limb bud mesenchymal cells: an in vitro model of endochondral skeletal development.

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Authors:  Brian D Larsen; Shravanti Rampalli; Leanne E Burns; Steve Brunette; F Jeffrey Dilworth; Lynn A Megeney
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-16       Impact factor: 11.205

9.  The pattern recognition receptor CD36 is a chondrocyte hypertrophy marker associated with suppression of catabolic responses and promotion of repair responses to inflammatory stimuli.

Authors:  Denise L Cecil; C Thomas G Appleton; Monika D Polewski; John S Mort; Ann Marie Schmidt; Alison Bendele; Frank Beier; Robert Terkeltaub
Journal:  J Immunol       Date:  2009-04-15       Impact factor: 5.422

10.  Activation of caspases is required for osteoblastic differentiation.

Authors:  Makio Mogi; Akifumi Togari
Journal:  J Biol Chem       Date:  2003-09-03       Impact factor: 5.157

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6.  Caspase Inhibition Affects the Expression of Autophagy-Related Molecules in Chondrocytes.

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7.  Distal-Less Homeobox 5 Is a Therapeutic Target for Attenuating Hypertrophy and Apoptosis of Mesenchymal Progenitor Cells.

Authors:  John Twomey-Kozak; Salomi Desai; Wenguang Liu; Neill Y Li; Nicholas Lemme; Qian Chen; Brett D Owens; Chathuraka T Jayasuriya
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