Staniszewska Izabela, Sariyer Ilker K, Lecht Shimon, Brown Meghan C, Walsh Erin M, Tuszynski George P, Safak Mahmut, Lazarovici Philip, Marcinkiewicz Cezary
Department of Neuroscience, Center for Neurovirology and Cancer Biology, Temple University, School of Medicine, Philadelphia, PA 19122, USA.
J Cell Sci. 2008 Feb 15;121(Pt 4):504-13. doi: 10.1242/jcs.000232. Epub 2008 Jan 29.
The integrin alpha9beta1 is a multifunctional receptor that interacts with a variety of ligands including vascular cell adhesion molecule 1, tenascin C and osteopontin. We found that this integrin is a receptor for nerve growth factor (NGF) and two other neurotrophins, brain-derived neurotrophic factor and NT3, using a cell adhesion assay with the alpha9SW480 cell line. Interaction of alpha9beta1 with NGF was confirmed in an ELISA assay by direct binding to purified integrin. alpha9beta1 integrin binds to neurotrophins in a manner similar to another common neurotrophin receptor, p75(NTR) (NGFR), although alpha9beta1 activity is correlated with induction of pro-survival and pro-proliferative signaling cascades. This property of alpha9beta1 resembles the interaction of NGF with a high affinity receptor, TrkA, however, this integrin shows a low affinity for NGF. NGF induces chemotaxis of cells expressing alpha9beta1 and their proliferation. Moreover, alpha9beta1 integrin is a signaling receptor for NGF, which activates the MAPK (Erk1/2) pathway. The alpha9beta1-dependent chemotactic ability of NGF appears to result from the activation of paxillin.
整合素α9β1是一种多功能受体,可与多种配体相互作用,包括血管细胞黏附分子1、腱生蛋白C和骨桥蛋白。我们使用α9SW480细胞系进行细胞黏附试验发现,这种整合素是神经生长因子(NGF)以及另外两种神经营养因子——脑源性神经营养因子和NT3的受体。通过与纯化的整合素直接结合的ELISA试验证实了α9β1与NGF的相互作用。α9β1整合素以类似于另一种常见神经营养因子受体p75(NTR)(NGFR)的方式与神经营养因子结合,尽管α9β1的活性与促生存和促增殖信号级联反应的诱导相关。α9β1的这一特性类似于NGF与高亲和力受体TrkA的相互作用,然而,这种整合素对NGF显示出低亲和力。NGF诱导表达α9β1的细胞发生趋化作用并使其增殖。此外,α9β1整合素是NGF的信号受体,可激活MAPK(Erk1/2)途径。NGF依赖α9β1的趋化能力似乎是由桩蛋白的激活所致。