2007
DOI: 10.1016/j.yexcr.2006.10.019
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Skeletal muscle stem cells express anti-apoptotic ErbB receptors during activation from quiescence

Abstract: (2007

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Cited by 59 publications
(41 citation statements)
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References 70 publications
(5 reference statements)
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“…This possibility is supported by the phenotypes observed in embryos overexpressing the inhibitor of apoptosis, DIAP1, as well as in mutants of different inducers of apoptosis. Of interest, a similar anti-apoptotic effect of the EGF pathway on activated satellite cells has been recently reported (Golding et al, 2007). These results provide additional evidence that Drosophila AMPs behave like vertebrate satellite cells and indicate that gaining insight into the genetic control of AMPs specification, proliferation, and survival may help in our understanding of muscle stem cell biology in general.…”
Section: Drosophila An Emerging Model To Study Muscle Stem Cellssupporting
confidence: 71%
“…This possibility is supported by the phenotypes observed in embryos overexpressing the inhibitor of apoptosis, DIAP1, as well as in mutants of different inducers of apoptosis. Of interest, a similar anti-apoptotic effect of the EGF pathway on activated satellite cells has been recently reported (Golding et al, 2007). These results provide additional evidence that Drosophila AMPs behave like vertebrate satellite cells and indicate that gaining insight into the genetic control of AMPs specification, proliferation, and survival may help in our understanding of muscle stem cell biology in general.…”
Section: Drosophila An Emerging Model To Study Muscle Stem Cellssupporting
confidence: 71%
“…6). It also turns out that the anti-apoptotic role of the EGFR pathway in Drosophila AMPs described here is conserved across evolution, as EGF signalling also promotes survival of vertebrate satellite cells (Golding et al, 2007).…”
Section: Egf Signalling Is Required For Specification and Maintenancementioning
confidence: 71%
“…Proteoglycans reside on the surface of satellite cells and function as receptors to bind a suite of secreted, yet inactive growth factor precursors. These precursors, including HGF (521), basic fibroblast growth factor (bFGF) (141), epidermal growth factor (EGF) (193), insulin-like growth factor isoforms (IGF-I, IGF-II) (323) and various Wnt glycoproteins (65,293), originate from either satellite cells, myofibers, interstitial cells, or serum. In resting muscle, the sequestering of inactive growth factors exists as a local reservoir, to facilitate a rapid response to muscle injury.…”
Section: Ecm and Associated Factorsmentioning
confidence: 99%