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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
要旨

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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製品内容

Sigma-Aldrich
抗アクチン抗体、クローンC4, ascites fluid, clone C4, Chemicon®
Sigma-Aldrich
抗脳由来神経栄養因子抗体, Chemicon®, from sheep
Sigma-Aldrich
抗神経成長因子受容体抗体、p75, serum, Chemicon®
Sigma-Aldrich
抗神経成長因子レセプター(NGFR p75) ウサギ宿主抗体, affinity isolated antibody, buffered aqueous solution
Sigma-Aldrich
Anti-Brain Derived Neurotrophic Factor Antibody, pro, Chemicon®, from rabbit