Department of Orthopedic Surgery, The First Affiliated Hospital, Jilin University, Changchun, Peoples Republic of China.
Cell Biol Int. 2011 Jun;35(6):569-74. doi: 10.1042/CBI20100431.
The MICA (MHC class I chain-related molecule A) is a ligand for the activating immunoreceptor NKG2D (natural killer group 2, member D). NKG2D recognizes MICA expressing at the cell surface for cell elimination. Although MICA is overexpressed in many kinds of tumours, tumour cells can cleverly escape immunosurveillance. One underlying mechanism for immunoescape is tumour-derived MICA shedding. In this study, we report that osteosarcoma-derived MICA results from proteolytic cleavage of MICA α3 ectodomain. sMICA (soluble MICA) might be released in the early stage of disease. A MMP9 (matrix metalloproteinase 9, gelatinase B)-specific inhibitor suppressed sMICA release, indicating that MMP9 is critically involved in the osteosarcoma-associated proteolytic release of sMICA, which facilitates tumour immune escape. Using a specific MMP inhibitor might represent a double-edged sword, where it can inhibit tumour invasion and restore antitumour immune response.
MICA(主要组织相容性复合体 I 类链相关分子 A)是激活免疫受体 NKG2D(自然杀伤细胞组 2,成员 D)的配体。NKG2D 识别细胞表面表达的 MICA 以进行细胞消除。尽管 MICA 在许多类型的肿瘤中过表达,但肿瘤细胞可以巧妙地逃避免疫监视。免疫逃避的一个潜在机制是肿瘤衍生的 MICA 脱落。在这项研究中,我们报告骨肉瘤衍生的 MICA 是通过 MICA α3 胞外结构域的蛋白水解切割产生的。sMICA(可溶性 MICA)可能在疾病的早期释放。一种 MMP9(基质金属蛋白酶 9,明胶酶 B)特异性抑制剂抑制 sMICA 的释放,表明 MMP9 参与骨肉瘤相关的 sMICA 蛋白水解释放,这有助于肿瘤免疫逃逸。使用特定的 MMP 抑制剂可能是一把双刃剑,它可以抑制肿瘤侵袭并恢复抗肿瘤免疫反应。