State Key Laboratory of Molecular Biology, National Center for Protein Science Shanghai, Shanghai Science Research Center, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China; University of Chinese Academy of Sciences, Shanghai 200031, China.
State Key Laboratory of Molecular Biology, National Center for Protein Science Shanghai, Shanghai Science Research Center, CAS Center for Excellence in Molecular Cell Science, Shanghai Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai 200031, China.
J Biol Chem. 2019 Dec 6;294(49):18881-18897. doi: 10.1074/jbc.RA119.010110. Epub 2019 Oct 25.
Scavenger receptor class A member 1 (SCARA1 or CD204) is an immune receptor highly expressed on macrophages. It forms homotrimers on the cell surface and plays important roles in regulating immune responses via its involvement in multiple pathways. However, both the structure and the functional roles of SCARA1 are not fully understood. Here, we determined the crystal structure of the C-terminal SRCR domain of SCARA1 at 1.8 Å resolution, revealing its Ca-binding site. Results from cell-based assays revealed that SCARA1 can recognize dead cells, rather than live cells, specifically through its SRCR domain and in a Ca-dependent manner. Furthermore, by combining MS and biochemical assays, we found that cellular spectrin is the binding target of SCARA1 on dead cells and that the SRCR domain of SCARA1 recognizes the SPEC repeats of spectrin in the presence of Ca We also found that macrophages can internalize dead cells or debris from both erythrocytes and other cells through the interaction between SCARA1 and spectrin, suggesting that SCARA1 could function as a scavenging receptor that recognizes dead cells. These results suggest that spectrin, which is one of the major components of the cytoskeleton, acts as a cellular marker that enables the recognition of dead cells by the immune system.
清道夫受体家族 A 成员 1(SCARA1 或 CD204)是一种在巨噬细胞上高度表达的免疫受体。它在细胞表面形成同源三聚体,并通过参与多种途径在调节免疫反应中发挥重要作用。然而,SCARA1 的结构和功能作用尚不完全清楚。在这里,我们确定了 SCARA1 的 C 端 SRCR 结构域的晶体结构,分辨率为 1.8Å,揭示了其 Ca 结合位点。基于细胞的测定结果表明,SCARA1 可以通过其 SRCR 结构域和 Ca 依赖性方式特异性识别死亡细胞,而不是活细胞。此外,通过结合 MS 和生化测定,我们发现细胞血影蛋白是 SCARA1 在死亡细胞上的结合靶标,并且在 Ca 的存在下,SCARA1 的 SRCR 结构域识别血影蛋白的 SPEC 重复序列。我们还发现巨噬细胞可以通过 SCARA1 与血影蛋白之间的相互作用,内化来自红细胞和其他细胞的死亡细胞或碎片,这表明 SCARA1 可以作为一种识别死亡细胞的吞噬受体发挥作用。这些结果表明,血影蛋白作为细胞骨架的主要成分之一,充当细胞标记物,使免疫系统能够识别死亡细胞。