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First published online 7 October 2008
doi: 10.1242/jcs.036152

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The calpain small subunit regulates cell-substrate mechanical interactions during fibroblast migration

¹ Department of Biological Sciences, Wayne State University, Detroit, MI 48202, USA
² Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA
³ Department of Physiology, University of Massachusetts Medical School, Worcester, MA 01605, USA
⁴ Department of Pediatrics and Pharmacology, University of Wisconsin Medical School, Madison, WI 53706, USA
⁵ Department of Biochemistry, Queen's University, Kingston, Ontario, K7L 3N6 Canada
⁶ Department of Pathology and Molecular Medicine, Cancer Research Institute, Queen's University, Kingston, Ontario, K7L 3N6 Canada

^* Author for correspondence (e-mail: beningo{at}wayne.edu)

Accepted 29 July 2008

Cell migration involves the dynamic formation and release of cell-substrate adhesions, where the exertion and detection of mechanical forces take place. Members of the calpain family of calcium-dependent proteases are believed to have a central role in these processes, possibly through the regulation of focal adhesion dynamics. The ubiquitous calpains, calpain 1 (µ-calpain) and calpain 2 (m-calpain), are heterodimers consisting of large catalytic subunits encoded by the Capn1 and Capn2 genes, respectively, and the small regulatory subunit encoded by Capn4. We have examined the role of the calpain regulatory small subunit in traction force production and mechanosensing during cell migration. Capn4-deficient or rescued cells were plated on flexible polyacrylamide substrates, for both the detection of traction forces and the application of mechanical stimuli. The total force output of Capn4-deficient cells was 75% lower than that of rescued cells and the forces were more randomly distributed and less dynamic in Capn4-deficient cells than in rescued cells. Furthermore, Capn4-deficient cells were less adhesive than wild-type cells and they also failed to respond to mechanical stimulations by pushing or pulling the flexible substrate, or by engaging dorsal receptors to the extracellular matrix. Surprisingly, fibroblasts deficient in calpain 1 or calpain 2 upon siRNA-mediated knockdown of Capn1 or Capn2, respectively, did not show the same defects in force production or adhesion, although they also failed to respond to mechanical stimulation. Interestingly, stress fibers were aberrant and also contained fewer colocalised vinculin-containing adhesions in Capn4-deficient cells than Capn1- and Capn2-knockdown cells. Together, these results suggest that the calpain small subunit plays an important role in the production of mechanical forces and in mediating mechanosensing during fibroblast migration. Furthermore, the Capn4 gene product might perform functions secondary to, or independent of, its role as a regulatory subunit for calpain 1 and calpain 2.

Key words: Calpain, Migration, Focal adhesions, Mechanosensing, Traction force

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