Editor’s Pick 2021: Highlights in Cell Adhesion and Migration

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Original Research
29 October 2020
The Planar Polarity Component VANGL2 Is a Key Regulator of Mechanosignaling
Sek-Shir Cheong
7 more and 
Charlotte H. Dean
A549 treated with actomyosin inhibitors phenocopy actin cytoskeleton and focal adhesion aberrations following siRNA knockdown of VANGL2. Representative images showing A549 transfected with (A) control siRNA or (B) VANGL2 siRNA. A549 labeled with phalloidin (magenta) to visualize F-actin and paxillin (green) for focal contacts. Nuclei were stained with DAPI (gray). Quantification of focal contact density (C) and mean focal contact size (micron2) (D) in control siRNA- or VANGL2 siRNA-treated A549 cells. n = 4 independent experiments; two technical replicates for each group per experiment; each dot represents mean value per experiment. Mann–Whitney U-test, ∗p < 0.05. Representative images showing control A549 without treatment (E), A549 treated with 25 μM blebbistastin for 30 min (F), 10 μM Y-27632 for 1 h (I), or 0.5 μM cytochalasin D for 30 min (L), and their corresponding focal contact density and mean focal contact size quantification (G,H,J,K,M,N). No morphological difference was observed in the DMEM-DMSO control or DMEM only control cells so only representative control cell images are shown. Cells were stained with phalloidin (magenta) and paxillin (green). Nuclei were stained with DAPI (gray). (O) Representative images showing wildtype and Vangl2Lp/+ TECs stained with pFAK-Y397 (green). Nuclei were stained with DAPI (gray). Representative western blots show the levels of pFAK-Y397 (green), total FAK (red), reference protein GAPDH (green) (P), and quantification of pFAK levels normalized to total FAK levels (Q). See Supplementary Figure S4 for whole western blot. n = 3 independent experiments. All data are presented as mean ± SEM.

VANGL2 is a component of the planar cell polarity (PCP) pathway, which regulates tissue polarity and patterning. The Vangl2Lp mutation causes lung branching defects due to dysfunctional actomyosin-driven morphogenesis. Since the actomyosin network regulates cell mechanics, we speculated that mechanosignaling could be impaired when VANGL2 is disrupted. Here, we used live-imaging of precision-cut lung slices (PCLS) from Vangl2Lp/+ mice to determine that alveologenesis is attenuated as a result of impaired epithelial cell migration. Vangl2Lp/+ tracheal epithelial cells (TECs) and alveolar epithelial cells (AECs) exhibited highly disrupted actomyosin networks and focal adhesions (FAs). Functional assessment of cellular forces confirmed impaired traction force generation in Vangl2Lp/+ TECs. YAP signaling in Vangl2Lp airway epithelium was reduced, consistent with a role for VANGL2 in mechanotransduction. Furthermore, activation of RhoA signaling restored actomyosin organization in Vangl2Lp/+, confirming RhoA as an effector of VANGL2. This study identifies a pivotal role for VANGL2 in mechanosignaling, which underlies the key role of the PCP pathway in tissue morphogenesis.

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Review
16 June 2020

Cell migration plays a critical role in vascular homeostasis. Under noxious stimuli, endothelial cells (ECs) migration always contributes to vascular repair, while enhanced migration of vascular smooth muscle cells (VSMCs) will lead to pathological vascular remodeling. Moreover, vascular activities are involved in communication between ECs and VSMCs, between ECs and immune cells, et al. Recently, Ma et al. (2015) discovered a novel migration-dependent organelle “migrasome,” which mediated release of cytoplasmic contents, and this process was defined as “migracytosis.” The formation of migrasome is precisely regulated by tetraspanins (TSPANs), cholesterol and integrins. Migrasomes can be taken up by neighboring cells, and migrasomes are distributed in many kinds of cells and tissues, such as in blood vessel, human serum, and in ischemic brain of human and mouse. In addition, the migrasome elements TSPANs are wildly expressed in cardiovascular system. Therefore, TSPANs, migrasomes and migracytosis might play essential roles in regulating vascular homeostasis. In this review, we will discuss the discoveries of migration-dependent migrasome and migracytosis, migrasome formation, the basic differences between migrasomes and exosomes, the distributions and functions of migrasome, the functions of migrasome elements TSPANs in vascular biology, and discuss the possible roles of migrasomes and migracytosis in vascular homeostasis.

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