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Mol Cell. 2000 Jan;5(1):27-34.

Microtubule binding to Smads may regulate TGF beta activity.

Author information

1
Department of Internal Medicine, College of Medicine and Public Health, Ohio State University, Columbus 43210, USA.

Abstract

Smad proteins are intracellular signaling effectors of the TGF beta superfamily. We show that endogenous Smad2, 3, and 4 bind microtubules (MTs) in several cell lines. Binding of Smads to MTs does not require TGF beta stimulation. TGF beta triggers dissociation from MTs, phosphorylation, and nuclear translocation of Smad2 and 3, with consequent activation of transcription in CCL64 cells. Destabilization of the MT network by nocodazole, colchicine, or a tubulin mutant disrupts the complex between Smads and MTs and increases TGF beta-induced Smad2 phosphorylation and transcriptional response in CCL64 cells. These data demonstrate that MTs may serve as a cytoplasmic sequestering network for Smads, controlling Smad2 association with and phosphorylation by activated TGF beta receptor I, and suggest a novel mechanism for the MT network to negatively regulate TGF beta function.

PMID:
10678166
DOI:
10.1016/s1097-2765(00)80400-1
[Indexed for MEDLINE]
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