Burnett D, Abrahamson M, Devalia J L, Sapsford R J, Davies R J, Buttle D J
Department of Immunology, University of Birmingham, United Kingdom.
Arch Biochem Biophys. 1995 Feb 20;317(1):305-10. doi: 10.1006/abbi.1995.1167.
Procathepsin B and cystatin C are found in human lung secretions. We investigated the capacity of human bronchial epithelial cells to synthesize and secrete these proteins. Immunoprecipitation of [35S]methionine-labeled proteins from cultured bronchial epithelial cell lysates, followed by denaturing gel electrophoresis and autoradiography, showed the presence of newly synthesized procathepsin B of M(r) 42,000; no mature form was detected. Cathepsin B in conditioned medium from epithelial cells was tagged with benzyloxycarbonyl-125I-tyrosyl-alanine-diazomethane before and after treatment of the medium with neutrophil elastase. Control medium again showed a predominant form of cathepsin B with a M(r) of 42,000, but upon treatment with neutrophil elastase this protein was converted to a M(r) of 38,000, similar to the active form previously found in lung secretions, and cathepsin B activity was generated. The medium also contained the cathepsin B inhibitor, cystatin C, but cystatins A, B, S, SN, SA, and kininogen were not detected. After removal of cystatin C from the medium, elastase was still required to activate procathepsin B. These results suggest that bronchial epithelial cells are a source of procathepsin B and cystatin C in lung secretions. Cleavage both of cystatin C and procathepsin B by neutrophil elastase is essential for the generation of cathepsin B activity in the medium.
组织蛋白酶原B和胱抑素C存在于人类肺分泌物中。我们研究了人类支气管上皮细胞合成和分泌这些蛋白质的能力。对来自培养的支气管上皮细胞裂解物的[35S]甲硫氨酸标记蛋白进行免疫沉淀,随后进行变性凝胶电泳和放射自显影,结果显示存在新合成的分子量为42,000的组织蛋白酶原B;未检测到成熟形式。在用中性粒细胞弹性蛋白酶处理培养基前后,用苄氧羰基-125I-酪氨酰-丙氨酸重氮甲烷标记上皮细胞条件培养基中的组织蛋白酶B。对照培养基再次显示出分子量为42,000的主要组织蛋白酶B形式,但在用中性粒细胞弹性蛋白酶处理后,该蛋白转化为分子量为38,000的形式,类似于先前在肺分泌物中发现的活性形式,并产生了组织蛋白酶B活性。培养基中还含有组织蛋白酶B抑制剂胱抑素C,但未检测到胱抑素A、B、S、SN、SA和激肽原。从培养基中去除胱抑素C后,仍需要弹性蛋白酶来激活组织蛋白酶原B。这些结果表明,支气管上皮细胞是肺分泌物中组织蛋白酶原B和胱抑素C的来源。中性粒细胞弹性蛋白酶对胱抑素C和组织蛋白酶原B的切割对于培养基中组织蛋白酶B活性的产生至关重要。