Department of Pediatrics, Neuroscience Program, and Colorado Intellectual and Developmental Disabilities Research Center, University of Colorado School of Medicine, Aurora, Colorado, USA.
J Neurochem. 2012 Mar;120(6):974-84. doi: 10.1111/j.1471-4159.2012.07651.x. Epub 2012 Feb 6.
The repellent semaphorin 3A (Sema3A) causes growth cone turning or collapse by triggering cytoskeletal rearrangements and detachment of adhesion sites. Growth cone detachment is dependent on eicosanoid activation of protein kinase C epsilon (PKCε), but the characterization of the phospholipase A(2) (PLA(2) ) that releases arachidonic acid (AA) for eicosanoid synthesis has remained elusive. Here, we show, in rat dorsal root ganglion (DRG) neurons, that Sema3A stimulates PLA(2) activity, that Sema3A-induced growth cone turning and collapse are dependent on the release of AA, and that the primary PLA(2) involved is the group IV α isoform (GIVA). Silencing GIVA expression renders growth cones resistant to Sema3A-induced collapse, and GIVA inhibition reverses Sema3A-induced repulsion into attraction. These studies identify a novel, early step in Sema3A-signaling and a PLA(2) necessary for growth cone repulsion and collapse.
repulsive semaphorin 3A (Sema3A) 通过触发细胞骨架重排和黏附位点的脱离,导致生长锥的转向或崩溃。生长锥的脱离依赖于类二十烷酸激活蛋白激酶 C ɛ (PKCε),但释放花生四烯酸 (AA) 用于类二十烷酸合成的磷脂酶 A(2) (PLA(2) ) 的特征仍然难以捉摸。在这里,我们在大鼠背根神经节 (DRG) 神经元中表明,Sema3A 刺激 PLA(2)活性,Sema3A 诱导的生长锥转向和崩溃依赖于 AA 的释放,而涉及的主要 PLA(2)是第四组 α 同工型 (GIVA)。沉默 GIVA 表达使生长锥对 Sema3A 诱导的崩溃具有抗性,并且 GIVA 抑制将 Sema3A 诱导的排斥作用反转成吸引作用。这些研究确定了 Sema3A 信号的一个新的、早期步骤,以及生长锥排斥和崩溃所必需的 PLA(2)。