Liu Z, Zhou X, Shapiro S D, Shipley J M, Twining S S, Diaz L A, Senior R M, Werb Z
Department of Dermatology, University of North Carolina, Chapel Hill 27599, USA.
Cell. 2000 Sep 1;102(5):647-55. doi: 10.1016/s0092-8674(00)00087-8.
We have identified the key protein substrate of gelatinase B/MMP-9 (GB) that is cleaved in vivo during dermal-epidermal separation triggered by antibodies to the hemidesmosomal protein BP180 (collagen XVII, BPAG2). Mice deficient in either GB or neutrophil elastase (NE) are resistant to blister formation in response to these antibodies in a mouse model of the autoimmune disease bullous pemphigoid. Disease develops upon complementation of GB -/- mice with NE -/- neutrophils or NE -/- mice with GB -/- neutrophils. Only NE degrades BP180 and produces dermal-epidermal separation in vivo and in culture. Instead, GB acts upstream to regulates NE activity by inactivating alpha1-proteinase inhibitor (alpha1-PI). Excess NE produces lesions in GB -/- mice without cleaving alpha1-PI. Excess alpha1-PI phenocopies GB and NE deficiency in wild-type mice.
我们已经鉴定出明胶酶B/基质金属蛋白酶-9(GB)的关键蛋白底物,该底物在由针对半桥粒蛋白BP180(胶原蛋白XVII,BPAG2)的抗体引发的真皮-表皮分离过程中在体内被切割。在自身免疫性疾病大疱性类天疱疮的小鼠模型中,缺乏GB或中性粒细胞弹性蛋白酶(NE)的小鼠对这些抗体引起的水疱形成具有抗性。在用NE-/-中性粒细胞补充GB-/-小鼠或用GB-/-中性粒细胞补充NE-/-小鼠后疾病会发展。只有NE能降解BP180并在体内和培养物中产生真皮-表皮分离。相反,GB通过使α1-蛋白酶抑制剂(α1-PI)失活在NE活性调节的上游起作用。过量的NE在GB-/-小鼠中产生病变而不切割α1-PI。过量的α1-PI在野生型小鼠中模拟GB和NE缺乏的表型。