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Merck

Motoneuron programmed cell death in response to proBDNF.

Developmental neurobiology (2011-08-13)
Anna R Taylor, David J Gifondorwa, Mac B Robinson, Jane L Strupe, David Prevette, James E Johnson, Barbara Hempstead, Ronald W Oppenheim, Carolanne E Milligan
RESUMO

Motoneurons (MN) as well as most neuronal populations undergo a temporally and spatially specific period of programmed cell death (PCD). Several factors have been considered to regulate the survival of MNs during this period, including availability of muscle-derived trophic support and activity. The possibility that target-derived factors may also negatively regulate MN survival has been considered, but not pursued. Neurotrophin precursors, through their interaction with p75(NTR) and sortilin receptors have been shown to induce cell death during development and following injury in the CNS. In this study, we find that muscle cells produce and secrete proBDNF. ProBDNF through its interaction with p75(NTR) and sortilin, promotes a caspase-dependent death of MNs in culture. We also provide data to suggest that proBDNF regulates MN PCD during development in vivo.

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Sigma-Aldrich
Anticorpo antiactina, clone C4, ascites fluid, clone C4, Chemicon®
Sigma-Aldrich
Anti-Brain Derived Neurotrophic Factor Antibody, Chemicon®, from sheep
Sigma-Aldrich
Anticorpo antirreceptor do fator de crescimento nervoso, p75, serum, Chemicon®
Sigma-Aldrich
Anti-Nerve Growth Factor Receptor (NGFR p75) antibody produced in rabbit, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
Anti-Brain Derived Neurotrophic Factor Antibody, pro, Chemicon®, from rabbit