Palecek S P, Huttenlocher A, Horwitz A F, Lauffenburger D A
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
J Cell Sci. 1998 Apr;111 ( Pt 7):929-40. doi: 10.1242/jcs.111.7.929.
Cell migration can be considered as a repeated cycle of membrane protrusion and attachment, cytoskeletal contraction and rear detachment. At intermediate and high levels of cell-substratum adhesiveness, cell speed appears to be rate-limited by rear detachment, specifically by the disruption of cytoskeleton-adhesion receptor-extracellular matrix (ECM) linkages. Often, cytoskeletal linkages fracture to release integrin adhesion receptors from the cell. Cell-extracellular matrix bonds may also dissociate, allowing the integrins to remain with the cell. To investigate molecular mechanisms involved in fracturing these linkages and regulating cell speed, we have developed an experimental system to track integrins during the process of rear retraction in Chinese hamster ovary (CHO) cells. Integrin expression level was varied by transfecting CHO B2 cells, which express very little endogenous alpha5 integrin, with a plasmid containing human alpha5 integrin cDNA and sorting the cells into three populations with different alpha5 expression levels. Receptor/ligand affinity was varied using CHO cells transfected with either alphaIIbbeta3 or alphaIIbbeta3(beta1-2), a high affinity variant. alphaIIbbeta3(beta1-2) is activated to a higher affinity state with an anti-LIBS2 antibody. Fluorescent probes were conjugated to non-adhesion perturbing anti-integrin antibodies, which label integrins in CHO cells migrating on a matrix-coated glass coverslip. The rear retraction area was determined using phase contrast microscopy and integrins initially in this area were tracked by fluorescence microscopy and a cooled CCD camera. We find that rear retraction rate appears to limit cell speed at intermediate and high adhesiveness, but not at low adhesiveness. Upon rear retraction, the amount of integrin released from the cell increases as extracellular matrix concentration, receptor level and receptor-ligand affinity increase. In fact, integrin release is a constant function of cell-substratum adhesiveness and the number of cell-substratum bonds. In the adhesive regime where rear detachment limits the rate of cell migration, cell speed has an inverse relationship to the amount of integrin released at the rear of the cell. At high cell-substratum adhesiveness, calpain, a Ca2+-dependent protease, is also involved in release of cytoskeletal linkages during rear retraction. Inhibition of calpain results in decreased integrin release from the cell membrane, and consequently a decrease in cell speed, during migration. These observations suggest a model for rear retraction in which applied tension and calpain-mediated cytoskeletal linkage cleavage are required at high adhesiveness, but only applied tension is required at low adhesiveness.
细胞迁移可被视为一个由膜突出与附着、细胞骨架收缩及后端脱离所组成的重复循环过程。在中等及高等细胞 - 基质黏附水平下,细胞速度似乎受限于后端脱离,具体而言是受细胞骨架 - 黏附受体 - 细胞外基质(ECM)连接的破坏所限。通常,细胞骨架连接断裂,使整合素黏附受体从细胞上释放。细胞 - 细胞外基质键也可能解离,使得整合素仍与细胞相连。为了研究这些连接断裂及调节细胞速度所涉及的分子机制,我们开发了一个实验系统,用于在中国仓鼠卵巢(CHO)细胞后端回缩过程中追踪整合素。通过用含有人α5整合素cDNA的质粒转染表达极少内源性α5整合素的CHO B2细胞,并将细胞分选成具有不同α5表达水平的三个群体,从而改变整合素表达水平。使用转染了αIIbβ3或αIIbβ3(β1 - 2)(一种高亲和力变体)的CHO细胞来改变受体/配体亲和力。αIIbβ3(β1 - 2)用抗LIBS2抗体激活至高亲和力状态。将荧光探针与非黏附干扰性抗整合素抗体偶联,这些抗体可标记在基质包被的玻璃盖玻片上迁移的CHO细胞中的整合素。使用相差显微镜确定后端回缩区域,并通过荧光显微镜和冷却的电荷耦合器件(CCD)相机追踪该区域最初的整合素。我们发现,在中等和高黏附性条件下,后端回缩速率似乎限制细胞速度,但在低黏附性条件下则不然。后端回缩时,从细胞释放的整合素量随着细胞外基质浓度、受体水平和受体 - 配体亲和力的增加而增加。实际上,整合素释放是细胞 - 基质黏附性和细胞 - 基质键数量的恒定函数。在后端脱离限制细胞迁移速率的黏附状态下,细胞速度与细胞后端释放的整合素量呈反比关系。在高细胞 - 基质黏附性时,钙蛋白酶(一种Ca2 +依赖性蛋白酶)也参与后端回缩过程中细胞骨架连接的释放。在迁移过程中,抑制钙蛋白酶会导致整合素从细胞膜的释放减少,进而导致细胞速度降低。这些观察结果提示了一个后端回缩模型,即在高黏附性时需要施加张力和钙蛋白酶介导的细胞骨架连接断裂,但在低黏附性时仅需要施加张力。