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PMID: 15541348 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Stabilization, not polymerization, of microtubules inhibits the nuclear translocation of STATs in adipocytes.

Biochemical and biophysical research communications ·Vol. 325 ·No. 3 ·2004-12-17 ·Pages 716-8

Gleason EL, Hogan JC, Stephens JM

Abstract

Signal transducers and activators of transcriptions (STATs) are a family of latent transcription factors which are activated by a variety of growth factors and cytokines in many cell types. However, the mechanism by which these transcription factors translocate to the nucleus is poorly understood. The goal of this study was to determine the requirement of microfilaments and microtubules for cytokine induced STAT activation in cultured adipocytes. We used seven different actin-specific and microtubule-specific agents that are well-established effectors of these cytoskeletal networks. Our results clearly demonstrate that inhibition of microfilaments or the prevention of microtubule polymerization has no effect on the ability of STATs to be tyrosine phosphorylated or to translocate to the nucleus. However, we observed that paclitaxel, a microtubule stabilizer, resulted in a significant decrease in the nuclear translocation of STATs without affecting the cytosolic tyrosine phosphorylation of these transcription factors. In summary, our results demonstrate that the dynamic instability, but not the polymerization, of microtubules contributes to nuclear translocation of STAT proteins in adipocytes.

MeSH Terms
3T3-L1 Cells Actin Cytoskeleton/drug effects,metabolism Active Transport, Cell Nucleus/drug effects,physiology Adaptor Proteins, Signal Transducing/metabolism Adipocytes/drug effects,metabolism Animals Cytochalasins/pharmacology Mice Microtubules/drug effects,metabolism Paclitaxel/pharmacology Polymers/metabolism Signal Transduction/drug effects,physiology
Chemicals
Adaptor Proteins, Signal Transducing Cytochalasins Polymers Paclitaxel
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Gleason Evanna L
Department of Biological Sciences, Louisiana State University, 202 Life Sciences Bldg., Baton Rouge, LA 70803, USA.
Hogan Jessica C
Stephens Jacqueline M
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
2004-12-17
Pages
716-8
Language
English
Region
United States
NLM ID
0372516
Subset
IM
Grants
NIDDK NIH HHS · R01 DK52968-02 · United States
NEI NIH HHS · R01 EY012204 · United States
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