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角质形成细胞纤溶酶原激活物抑制剂的特性及一种纯化的纤溶酶原激活物抑制剂预防天疱疮IgG诱导的棘层松解的证明

Characterization of keratinocyte plasminogen activator inhibitors and demonstration of the prevention of pemphigus IgG-induced acantholysis by a purified plasminogen activator inhibitor.

作者信息

Hashimoto K, Wun T C, Baird J, Lazarus G S, Jensen P J

机构信息

Department of Dermatology, University of Pennsylvania, Philadelphia 19104.

出版信息

J Invest Dermatol. 1989 Mar;92(3):310-4. doi: 10.1111/1523-1747.ep12277087.

Abstract

To investigate the mechanisms by which cutaneous plasminogen activator (PA) may be regulated, we have tested cultured keratinocytes for the presence of PA inhibitors. Using biosynthetic labeling experiments with 35S-methionine in conjunction with specific antibody precipitation, we have shown that human keratinocytes in culture synthesized and secreted both PA inhibitor 1 and PA inhibitor 2. PA inhibitor 1 was present in conditioned media in the inactive form, but it could be detected with reverse phase autography. PA inhibitor 2 was detected by its ability to form complexes with 125I-uPA. Potential therapeutic relevance for cutaneous PA inhibitor 2 was suggested in skin organ culture experiments which demonstrated that purified PA inhibitor 2 from human placenta was able to prevent the acantholytic changes induced by pemphigus IgG.

摘要

为了研究皮肤纤溶酶原激活剂(PA)可能的调节机制,我们检测了培养的角质形成细胞中PA抑制剂的存在情况。通过使用35S-甲硫氨酸进行生物合成标记实验并结合特异性抗体沉淀,我们发现培养的人角质形成细胞合成并分泌了PA抑制剂1和PA抑制剂2。PA抑制剂1以无活性形式存在于条件培养基中,但可通过反相自显影检测到。PA抑制剂2通过其与125I-uPA形成复合物的能力来检测。皮肤器官培养实验表明,从人胎盘中纯化的PA抑制剂2能够预防天疱疮IgG诱导的棘层松解变化,这提示了皮肤PA抑制剂2潜在的治疗意义。

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