α4/α9 Integrins Coordinate Epithelial Cell Migration Through Local Suppression of MAP Kinase Signaling Pathways

Adhesion of basal keratinocytes to the underlying extracellular matrix (ECM) plays a key role in the control of skin homeostasis and response to injury. Integrin receptors indirectly link the ECM to the cell cytoskeleton through large protein complexes called focal adhesions (FA). FA also function as intracellular biochemical signaling platforms to enable cells to respond to changing extracellular cues. The alpha 4 beta 1 and alpha 9 beta 1 integrins are both expressed in basal keratinocytes, share some common ECM ligands, and have been shown to promote wound healing in vitro and in vivo. However, their roles in maintaining epidermal homeostasis and relative contributions to pathological processes in the skin remain unclear. We found that alpha 4 beta 1 and alpha 9 beta 1 occupied distinct regions in monolayers of a basal keratinocyte cell line (NEB-1). During collective cell migration (CCM), alpha 4 and alpha 9 integrins co-localized along the leading edge. Pharmacological inhibition of alpha 4 beta 1 and alpha 9 beta 1 integrins increased keratinocyte proliferation and induced a dramatic change in cytoskeletal remodeling and FA rearrangement, detrimentally affecting CCM. Further analysis revealed that alpha 4 beta 1/alpha 9 beta 1 integrins suppress extracellular signal-regulated kinase (ERK1/2) activity to control migration through the regulation of downstream kinases including Mitogen and Stress Activated Kinase 1 (MSK1). This work demonstrates the roles of alpha 4 beta 1 and alpha 9 beta 1 in regulating migration in response to damage cues.

Automated summary

The adhesion of basal keratinocytes to the ECM through integrin receptors is crucial for skin homeostasis and response to injury. Alpha 4 beta 1 and alpha 9 beta 1 integrins play roles in regulating migration by suppressing ERK1/2 activity and controlling downstream kinases like MSK1.