Go Mandy Y, Chow Edith M C, Mogridge Jeremy
Department of Laboratory Medicine and Pathobiology, Medical Sciences Building, Rm. 6308, 1 King's College Circle, University of Toronto, Toronto, ON, Canada M5S 1A8.
Infect Immun. 2009 Jan;77(1):52-9. doi: 10.1128/IAI.01073-08. Epub 2008 Oct 20.
The protective antigen (PA) component of anthrax toxin binds the I domain of the receptor ANTXR1. Integrin I domains convert between open and closed conformations that bind ligand with high and low affinities, respectively; this process is regulated by signaling from the cytoplasmic domains. To assess whether intracellular signals might influence the interaction between ANTXR1 and PA, we compared two splice variants of ANTXR1 that differ only in their cytoplasmic domains. We found that cells expressing ANTXR1 splice variant 1 (ANTXR1-sv1) bound markedly less PA than did cells expressing a similar level of the shorter splice variant ANTXR1-sv2. ANTXR1-sv1 but not ANTXR1-sv2 associated with the actin cytoskeleton, although disruption of the cytoskeleton did not affect binding of ANTXR-sv1 to PA. Introduction of a cytoplasmic domain missense mutation found in the related receptor ANTXR2 in a patient with juvenile hyaline fibromatosis impaired actin association and increased binding of PA to ANTXR1-sv1. These results suggest that ANTXR1 has two affinity states that may be modulated by cytoplasmic signals.
炭疽毒素的保护性抗原(PA)成分与受体ANTXR1的I结构域结合。整合素I结构域在开放和闭合构象之间转换,分别以高亲和力和低亲和力结合配体;这一过程受细胞质结构域信号传导的调节。为了评估细胞内信号是否可能影响ANTXR1与PA之间的相互作用,我们比较了ANTXR1的两种剪接变体,它们仅在细胞质结构域有所不同。我们发现,表达ANTXR1剪接变体1(ANTXR1-sv1)的细胞与PA的结合明显少于表达相似水平较短剪接变体ANTXR1-sv2的细胞。ANTXR1-sv1而非ANTXR1-sv2与肌动蛋白细胞骨架相关,尽管细胞骨架的破坏并不影响ANTXR-sv1与PA的结合。在一名青少年透明纤维瘤病患者中,相关受体ANTXR2中发现的细胞质结构域错义突变的引入损害了肌动蛋白的结合,并增加了PA与ANTXR1-sv1的结合。这些结果表明,ANTXR1有两种亲和力状态,可能受细胞质信号调节。