TY - JOUR
T1 - T-plastin is essential for basement membrane assembly and epidermal morphogenesis
AU - Dor-On, Eyal
AU - Raviv, Shaul
AU - Cohen, Yonatan
AU - Adir, Orit
AU - Padmanabhan, Krishnanand
AU - Luxenburg, Chen
N1 - Publisher Copyright:
© 2017 The Authors,.
PY - 2017/5/30
Y1 - 2017/5/30
N2 - The establishment of epithelial architecture is a complex process involving cross-talk between cells and the basement membrane. Basement membrane assembly requires integrin activity but the role of the associated actomyosin cytoskeleton is poorly understood. Here, we identify the actin-bundling protein T-plastin (Pls3) as a regulator of basement membrane assembly and epidermal morphogenesis. In utero depletion of Pls3 transcripts in mouse embryos caused basement membrane and polarity defects in the epidermis but had little effect on cell adhesion and differentiation. Loss-of-function experiments demonstrated that the apicobasal polarity defects were secondary to the disruption of the basementmembrane. However, the basement membrane itself was profoundly sensitive to subtle perturbations in the actin cytoskeleton.We further show that Pls3 localized to the cell cortex, where it was essential for the localization and activation of myosin II. Inhibition of myosin II motor activity disrupted basement membrane organization. Our results provide insights into the regulation of cortical actomyosin and its importance for basement membrane assembly and skin morphogenesis.
AB - The establishment of epithelial architecture is a complex process involving cross-talk between cells and the basement membrane. Basement membrane assembly requires integrin activity but the role of the associated actomyosin cytoskeleton is poorly understood. Here, we identify the actin-bundling protein T-plastin (Pls3) as a regulator of basement membrane assembly and epidermal morphogenesis. In utero depletion of Pls3 transcripts in mouse embryos caused basement membrane and polarity defects in the epidermis but had little effect on cell adhesion and differentiation. Loss-of-function experiments demonstrated that the apicobasal polarity defects were secondary to the disruption of the basementmembrane. However, the basement membrane itself was profoundly sensitive to subtle perturbations in the actin cytoskeleton.We further show that Pls3 localized to the cell cortex, where it was essential for the localization and activation of myosin II. Inhibition of myosin II motor activity disrupted basement membrane organization. Our results provide insights into the regulation of cortical actomyosin and its importance for basement membrane assembly and skin morphogenesis.
UR - http://www.scopus.com/inward/record.url?scp=85020137524&partnerID=8YFLogxK
U2 - 10.1126/scisignal.aal3154
DO - 10.1126/scisignal.aal3154
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C2 - 28559444
AN - SCOPUS:85020137524
SN - 1945-0877
VL - 10
JO - Science Signaling
JF - Science Signaling
IS - 481
M1 - aal3154
ER -