CED-10-WASP-Arp2/3 signaling axis regulates apoptotic cell corpse engulfment in C. elegans
Developmental Biology, ISSN: 0012-1606, Vol: 428, Issue: 1, Page: 215-223
2017
- 9Citations
- 32Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations9
- Citation Indexes9
- CrossRef7
- Captures32
- Readers32
- 32
Article Description
Efficient clearance of apoptotic cells is essential for tissue homeostasis in metazoans. Genetic studies in Caenorhabditis elegans have identified signaling cascades that activate CED-10/Rac1 GTPase and promote actin cytoskeletal rearrangement during apoptotic cell engulfment. However, the molecular connection between CED-10 activation and actin reorganization remains elusive. Here, we provide evidence that CED-10 binds to the Arp2/3 nucleation promoting factor WASP; CED-10 recruits WASP and Arp2/3 to apoptotic cell corpses in the phagocytes. The loss of WASP and Arp2/3 impaired cell corpse engulfment. Furthermore, we uncover that a WASP-activating factor SEM-5/GRB2 functions in the phagocytes to promote cell corpse clearance. Together, our results suggest CED-10 reorganizes the actin cytoskeleton by recruiting the WASP-Arp2/3 actin nucleation factors during apoptotic cell engulfment.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0012160617301987; http://dx.doi.org/10.1016/j.ydbio.2017.06.005; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85020777706&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/28602951; https://linkinghub.elsevier.com/retrieve/pii/S0012160617301987; https://dx.doi.org/10.1016/j.ydbio.2017.06.005
Elsevier BV
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