Please use this identifier to cite or link to this item:
|Title:||Genetic Dissection of Neurotrophin Signaling through the p75 Neurotrophin Receptor||Authors:||Charalampopoulos, I.
|Issue Date:||27-Dec-2012||Citation:||Charalampopoulos, I., Vicario, A., Pediaditakis, I., Gravanis, A., Simi, A., Ibáñez, C.F. (2012-12-27). Genetic Dissection of Neurotrophin Signaling through the p75 Neurotrophin Receptor. Cell Reports 2 (6) : 1563-1570. ScholarBank@NUS Repository. https://doi.org/10.1016/j.celrep.2012.11.009||Abstract:||Structural determinants underlying signaling specificity in the tumor necrosis factor receptor superfamily (TNFRSF) are poorly characterized, and it is unclear whether different signaling outputs can be genetically dissociated. The p75 neurotrophin receptor (p75NTR), also known as TNFRSF16, is a key regulator of trophic and injury responses in the nervous system. Here, we describe a genetic approach for dissecting p75NTR signaling and deciphering its underlying logic. Structural determinants important for regulation of cell death, NF-κB, and RhoA pathways were identified in the p75NTR death domain (DD). Proapoptotic and prosurvival pathways mapped onto nonoverlapping epitopes, demonstrating that different signaling outputs can be genetically separated in p75NTR. Dissociation of c-Jun kinase (JNK) and caspase-3 activities indicated that JNK is necessary but not sufficient for p75NTR-mediated cell death. RIP2 recruitment and RhoGDI release were mechanistically linked, indicating that competition for DD binding underlies crosstalk between NF-κB and RhoA pathways in p75NTR signaling. These results provide insights into the logic of p75NTR signaling and pave the way for a genetic dissection of p75NTR function and physiology.||Source Title:||Cell Reports||URI:||http://scholarbank.nus.edu.sg/handle/10635/127141||ISSN:||22111247||DOI:||10.1016/j.celrep.2012.11.009|
|Appears in Collections:||Staff Publications|
Show full item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.