학술논문

Bone morphogenetic protein-5 (BMP-5) promotes dendritic growth in cultured sympathetic neurons.
Document Type
article
Source
BMC neuroscience. 2(1)
Subject
Superior Cervical Ganglion
Neuroglia
Neurons
Dendrites
Sympathetic Nervous System
Cells
Cultured
Animals
Humans
Rats
Rats
Sprague-Dawley
Transforming Growth Factor beta
Proteins
Carrier Proteins
Follistatin
DNA-Binding Proteins
Trans-Activators
Bone Morphogenetic Proteins
Recombinant Fusion Proteins
RNA
Messenger
Coculture Techniques
Signal Transduction
Gene Expression Regulation
Developmental
Phosphorylation
Smad Proteins
Smad1 Protein
Bone Morphogenetic Protein 5
Bone Morphogenetic Protein 7
Cells
Cultured
Sprague-Dawley
RNA
Messenger
Gene Expression Regulation
Developmental
Neurology & Neurosurgery
Neurosciences
Cognitive Sciences
Biochemistry and Cell Biology
Language
Abstract
BackgroundBMP-5 is expressed in the nervous system throughout development and into adulthood. However its effects on neural tissues are not well defined. BMP-5 is a member of the 60A subgroup of BMPs, other members of which have been shown to stimulate dendritic growth in central and peripheral neurons. We therefore examined the possibility that BMP-5 similarly enhances dendritic growth in cultured sympathetic neurons.ResultsSympathetic neurons cultured in the absence of serum or glial cells do not form dendrites; however, addition of BMP-5 causes these neurons to extend multiple dendritic processes, which is preceded by an increase in phosphorylation of the Smad-1 transcription factor. The dendrite-promoting activity of BMP-5 is significantly inhibited by the BMP antagonists noggin and follistatin and by a BMPR-IA-Fc chimeric protein. RT-PCR and immunocytochemical analyses indicate that BMP-5 mRNA and protein are expressed in the superior cervical ganglia (SCG) during times of initial growth and rapid expansion of the dendritic arbor.ConclusionsThese data suggest a role for BMP-5 in regulating dendritic growth in sympathetic neurons. The signaling pathway that mediates the dendrite-promoting activity of BMP-5 may involve binding to BMPR-IA and activation of Smad-1, and relative levels of BMP antagonists such as noggin and follistatin may modulate BMP-5 signaling. Since BMP-5 is expressed at relatively high levels not only in the developing but also the adult nervous system, these findings suggest the possibility that BMP-5 regulates dendritic morphology not only in the developing, but also the adult nervous system.