Horiuchi Keisuke, Weskamp Gisela, Lum Lawrence, Hammes Hans-Peter, Cai Hui, Brodie Thomas A, Ludwig Thomas, Chiusaroli Riccardo, Baron Roland, Preissner Klaus T, Manova Katia, Blobel Carl P
Cellular Biochemistry and Biophysics Program, Sloan-Kettering Institute, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Mol Cell Biol. 2003 Aug;23(16):5614-24. doi: 10.1128/MCB.23.16.5614-5624.2003.
ADAM15 (named for a disintegrin and metalloprotease 15, metargidin) is a membrane-anchored glycoprotein that has been implicated in cell-cell or cell-matrix interactions and in the proteolysis of molecules on the cell surface or extracellular matrix. To characterize the potential roles of ADAM15 during development and in adult mice, we analyzed its expression pattern by mRNA in situ hybridization and generated mice carrying a targeted deletion of ADAM15 (adam15(-/-) mice). A high level of expression of ADAM15 was found in vascular cells, the endocardium, hypertrophic cells in developing bone, and specific areas of the hippocampus and cerebellum. However, despite the pronounced expression of ADAM15 in these tissues, no major developmental defects or pathological phenotypes were evident in adam15(-/-) mice. The elevated levels of ADAM15 in endothelial cells prompted an evaluation of its role in neovascularization. In a mouse model for retinopathy of prematurity, adam15(-/-) mice had a major reduction in neovascularization compared to wild-type controls. Furthermore, the size of tumors resulting from implanted B16F0 mouse melanoma cells was significantly smaller in adam15(-/-) mice than in wild-type controls. Since ADAM15 does not appear to be required for developmental angiogenesis or for adult homeostasis, it may represent a novel target for the design of inhibitors of pathological neovascularization.
ADAM15(因其包含去整合素和金属蛋白酶结构域15,即间胶素而得名)是一种膜锚定糖蛋白,与细胞间或细胞与基质的相互作用以及细胞表面或细胞外基质中分子的蛋白水解有关。为了表征ADAM15在发育过程中和成年小鼠中的潜在作用,我们通过mRNA原位杂交分析了其表达模式,并培育出携带ADAM15靶向缺失的小鼠(adam15(-/-)小鼠)。在血管细胞、心内膜、发育中的骨骼中的肥大细胞以及海马体和小脑的特定区域发现了高水平的ADAM15表达。然而,尽管ADAM15在这些组织中表达明显,但adam15(-/-)小鼠中并未出现明显的主要发育缺陷或病理表型。内皮细胞中ADAM15水平的升高促使人们评估其在新血管形成中的作用。在早产儿视网膜病变的小鼠模型中,与野生型对照相比,adam15(-/-)小鼠的新血管形成显著减少。此外,植入B16F0小鼠黑色素瘤细胞产生的肿瘤大小在adam15(-/-)小鼠中明显小于野生型对照。由于ADAM15似乎不是发育性血管生成或成年期稳态所必需的,它可能代表了设计病理性新血管形成抑制剂的一个新靶点。