Jia Zongjian, Vadnais Julie, Lu Michael L, Noël Josette, Nabi Ivan R
Department of Cellular and Physiological Sciences, Life Sciences Institute, University of British Columbia, Vancouver, BC, Canada V6T 1Z3.
Biol Cell. 2006 Jun;98(6):337-51. doi: 10.1042/BC20050088.
The c-Met-dependent, beta-actin-rich, blebbed pseudopodia of MSV-MDCK-INV (invasive Moloney-sarcoma-virus-transformed Madin-Darby canine kidney) cells are induced by Rho/ROCK (Rho kinase) activation, and are morphologically distinct from flat extended lamellipodia.
Microtubules were shown to extend to these actin-rich pseudopodial domains, and microtubule depolymerization by nocodazole treatment resulted in progressive cellular blebbing, initiating in the pseudopodial domains and resulting in transient cellular rounding and blebbing after 30 min. The blebbing response was dependent on autocrine HGF (hepatocyte growth factor) activation of c-Met and prevented by inhibition of RhoA, ROCK and p38 MAPK (p38 mitogen-activated protein kinase), but not ERK (extracellular-signal-regulated kinase) or PI3K (phosphoinositide 3-kinase). Phospho-p38 MAPK was present in pseudopodia, localizing activation of this signalling pathway to this protrusive membrane structure. In serum-starved cells, LPA (lysophosphatidic acid) activation of RhoA induced p38 MAPK-dependent pseudopodial protrusions, and inhibition of p38 MAPK prevented pseudopodial protrusion and displacement of MSV-MDCK-INV cells. MSV-MDCK-INV cells exhibited intermittent blebbing and rounding, which may represent an integral part of their motile behaviour.
The localized activation of an autocrine HGF/c-Met loop regulates Rho/ROCK activation of p38 MAPK signalling to stimulate both membrane blebbing and pseudopod formation.
MSV-MDCK-INV(侵袭性莫洛尼肉瘤病毒转化的马-达二氏犬肾细胞)细胞中依赖c-Met、富含β-肌动蛋白的泡状伪足由Rho/ROCK(Rho激酶)激活诱导产生,在形态上与扁平伸展的片状伪足不同。
微管被证明可延伸至这些富含肌动蛋白的伪足区域,用诺考达唑处理使微管解聚导致细胞逐渐出现泡状化,起始于伪足区域,30分钟后导致细胞短暂变圆并出现泡状化。泡状化反应依赖于c-Met的自分泌HGF(肝细胞生长因子)激活,并可通过抑制RhoA、ROCK和p38 MAPK(p38丝裂原活化蛋白激酶)来阻止,但不能通过抑制ERK(细胞外信号调节激酶)或PI3K(磷脂酰肌醇3激酶)来阻止。磷酸化的p38 MAPK存在于伪足中,将该信号通路的激活定位到这种突出的膜结构上。在血清饥饿的细胞中,RhoA的LPA(溶血磷脂酸)激活诱导p38 MAPK依赖的伪足突出,抑制p38 MAPK可阻止MSV-MDCK-INV细胞的伪足突出和移位。MSV-MDCK-INV细胞表现出间歇性的泡状化和变圆,这可能是其运动行为的一个组成部分。
自分泌HGF/c-Met环的局部激活调节Rho/ROCK对p38 MAPK信号通路的激活,以刺激膜泡状化和伪足形成。