AI Article Synopsis

  • During skin wound healing, keratinocytes reorganize their cellular structure by breaking down hemidesmosomes and altering their actin cytoskeleton to move effectively over the dermis.
  • Despite the disassembly, collagen XVII (ColXVII) remains in an actin-rich area behind the leading edge of the cell, where it interacts with actinin4.
  • Reducing ColXVII or actinin4 disrupts keratinocyte movement and increases the retrograde movement of actin bundles, highlighting the role of ColXVII-actinin4 complexes in controlling actin dynamics and the directional migration of keratinocytes.

Article Abstract

During wound healing of the skin, keratinocytes disassemble hemidesmosomes and reorganize their actin cytoskeletons in order to exert traction forces on and move directionally over the dermis. Nonetheless, the transmembrane hemidesmosome component collagen XVII (ColXVII) is found in actin-rich lamella, situated behind the lamellipodium. A set of actin bundles, along which ColXVII colocalizes with actinin4, is present at each lamella. Knockdown of either ColXVII or actinin4 not only inhibits directed migration of keratinocytes but also relieves constraints on actin bundle retrograde movement at the site of lamella, such that actin bundle movement is enhanced more than 5-fold. Moreover, whereas control keratinocytes move in a stepwise fashion over a substrate by generating alternating traction forces, of up to 1.4 kPa, at each flank of the lamellipodium, ColXVII knockdown keratinocytes fail to do so. In summary, our data indicate that ColXVII-actinin4 complexes at the lamella of a moving keratinocyte regulate actin dynamics, thereby determining the direction of cell movement.-Hiroyasu, S., Colburn, Z. T., Jones, J. C. R. A hemidesmosomal protein regulates actin dynamics and traction forces in motile keratinocytes.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871795PMC
http://dx.doi.org/10.1096/fj.201500160RDOI Listing

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