Kobayashi Norimoto, Karisola Piia, Peña-Cruz Victor, Dorfman David M, Jinushi Masahisa, Umetsu Sarah E, Butte Manish J, Nagumo Haruo, Chernova Irene, Zhu Baogong, Sharpe Arlene H, Ito Susumu, Dranoff Glenn, Kaplan Gerardo G, Casasnovas Jose M, Umetsu Dale T, Dekruyff Rosemarie H, Freeman Gordon J
Department of Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, Harvard Medical School, Boston, MA 02115, USA.
Immunity. 2007 Dec;27(6):927-40. doi: 10.1016/j.immuni.2007.11.011.
The T cell immunoglobulin mucin (TIM) proteins regulate T cell activation and tolerance. Here we showed that TIM-4 is expressed on human and mouse macrophages and dendritic cells, and both TIM-4 and TIM-1 specifically bound phosphatidylserine (PS) on the surface of apoptotic cells but not any other phospholipid tested. TIM-4(+) peritoneal macrophages, TIM-1(+) kidney cells, and TIM-4- or TIM-1-transfected cells efficiently phagocytosed apoptotic cells, and phagocytosis could be blocked by TIM-4 or TIM-1 monoclonal antibodies. Mutations in the unique cavity of TIM-4 eliminated PS binding and phagocytosis. TIM-4 mAbs that blocked PS binding and phagocytosis mapped to epitopes in this binding cavity. These results show that TIM-4 and TIM-1 are immunologically restricted members of the group of receptors whose recognition of PS is critical for the efficient clearance of apoptotic cells and prevention of autoimmunity.
T细胞免疫球蛋白黏蛋白(TIM)家族蛋白可调节T细胞的激活及耐受性。我们在此研究中发现,TIM-4在人和小鼠的巨噬细胞及树突状细胞上表达,且TIM-4和TIM-1均能特异性结合凋亡细胞表面的磷脂酰丝氨酸(PS),而不与所检测的其他任何磷脂结合。TIM-4阳性的腹膜巨噬细胞、TIM-1阳性的肾细胞以及转染了TIM-4或TIM-1的细胞均能有效吞噬凋亡细胞,且吞噬作用可被TIM-4或TIM-1单克隆抗体阻断。TIM-4独特腔体内的突变消除了PS结合及吞噬作用。阻断PS结合及吞噬作用的TIM-4单克隆抗体定位于此结合腔内的表位。这些结果表明,TIM-4和TIM-1是一组受体中在免疫方面具有特异性的成员,它们对PS的识别对于有效清除凋亡细胞及预防自身免疫至关重要。
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