Bone morphogenetic protein‐6 is a neurotrophic factor for calbindin‐positive striatal neurons

E Gratacos, N Gavalda, J Alberch - Journal of neuroscience …, 2002 - Wiley Online Library
E Gratacos, N Gavalda, J Alberch
Journal of neuroscience research, 2002Wiley Online Library
Bone morphogenetic proteins (BMPs) are a set of members of the transforming growth factor‐
β superfamily recently described as promoting the differentiation of several neuronal
populations within the basal ganglia. This study examined whether a member of this family,
BMP‐6, could exert neurotrophic effects on the neurons of the striatum, in which BMP‐6
mRNA had been previously detected during development. Here we show that BMP‐6
increases the number and differentiation of calbindin‐positive neurons in vitro. Indeed, BMP …
Abstract
Bone morphogenetic proteins (BMPs) are a set of members of the transforming growth factor‐β superfamily recently described as promoting the differentiation of several neuronal populations within the basal ganglia. This study examined whether a member of this family, BMP‐6, could exert neurotrophic effects on the neurons of the striatum, in which BMP‐6 mRNA had been previously detected during development. Here we show that BMP‐6 increases the number and differentiation of calbindin‐positive neurons in vitro. Indeed, BMP‐6 increased the total area, the perimeter, and the degree of arborization of this neuronal population. This trophic factor promoted dendritic growth without modifying axonal length or soma area. Furthermore, BMP‐6 increased the number of glial fibrillary acidic protein‐positive cells while decreasing the number of nestin‐positive cells. The suppression of cell proliferation or glial development by the antimitotic fluorodeoxyuridine removed the effects on striatal neurons, suggesting the involvement of astroglial cells in the differentiation induced by BMP‐6. The current results confirm the relevance of BMPs in the development of the striatum and emphasize the crucial importance of the trophic interaction between glial and neuronal cells. © 2002 Wiley‐Liss, Inc.
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