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Circulation Research. 2006;98:245-253
Published online before print December 15, 2005, doi: 10.1161/01.RES.0000200179.29375.cc
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(Circulation Research. 2006;98:245.)
© 2006 American Heart Association, Inc.


Cellular Biology

Functional TRPM7 Channels Accumulate at the Plasma Membrane in Response to Fluid Flow

Elena Oancea*, Joshua T. Wolfe*, David E. Clapham

From the Howard Hughes Medical Institute, Department of Cardiology, Children’s Hospital Boston, Harvard Medical School, Mass.

Correspondence to Elena Oancea, Howard Hughes Medical Institute, Department of Cardiology, Children’s Hospital Boston, Harvard Medical School, 320 Longwood Ave, Enders 1309, Boston, MA 02115. E-mail oancea{at}enders.tch.harvard.edu

Many cells are constantly exposed to fluid mechanical forces generated by flowing blood, and wall shear stresses modulate aspects of their structure and function. However, the mechanisms for mechanotransduction of flow are not well understood. Here we report that TRPM7, which is both an ion channel and a functional kinase, is translocated within cells in response to laminar flow. After exposure of cells to physiological values of laminar fluid flow, the number of TRPM7 molecules localized at or near the plasma membrane increased up to 2-fold, in less than 100 seconds. This increase in membrane-localized GFP-TRPM7, as seen by total internal reflection fluorescence microscopy, closely correlated with increases in TRPM7 current. Both endogenous and heterologously expressed TRPM7 was found in tubulovesicular structures that were translocated to the region of the plasma membrane on induction of shear stress. In vascular smooth muscle cells, but not in several types of endothelial cells, fluid flow increased endogenous native TRPM7 current amplitude. We hypothesize that TRPM7 plays a role in pathological response to vessel wall injury.


Key Words: TRP ion channels • TRPM7 • shear force • total internal reflection fluorescence (TIRF) microscopy • vascular smooth muscle cells


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