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一种培养的人皮肤上皮细胞系产生酸性和中性半胱氨酸蛋白酶抑制剂。

Production of acid and neutral cysteine-proteinase inhibitors by a cultured human skin epithelium cell line.

作者信息

Hopsu-Havu V K, Joronen I, Rinne A, Järvinen M

出版信息

Arch Dermatol Res. 1985;277(6):452-6. doi: 10.1007/BF00510062.

Abstract

Human skin epithelial-like cells (NCTC-strain 2544) were grown in RPMI-1640 medium supplemented with foetal calf serum for up to 2 weeks. The culture medium and extracts made from the cells were subjected to gel-filtration chromatography in a Sephacryl S-200 column for fractionation of the proteins. The fractions were assayed for acid and neutral cysteine-proteinase inhibitor (ACPI, NCPI) using time-resolved fluoroimmunoassay and radioimmunoassay, and the cysteine-proteinase-inhibiting activities were assayed using papain. Free NCPI, i.e. a molecule with isoelectric variants at pHs 6.0 and 6.5, which has an Mr of around 12,000 and is capable of inhibiting papain, was detected both in the culture medium and in the cells. Immunodiffusion studies revealed its immunological identity with human spleen-derived NCPI. The amount of NCPI increased during the incubation period. ACPI--characterized as a molecule having an isoelectric point of 4.9, an Mr of about 12,000, papain-inhibiting capacity and antigenic reactivity with spleen-derived ACPI--was not detected in the culture medium. It was, however, detected in the cells after 2 weeks in culture. These data prove that ACPI and NCPI are synthesized by the NCTC-2544 cells under the present culture conditions.

摘要

人皮肤上皮样细胞(NCTC - 2544株)在补充有胎牛血清的RPMI - 1640培养基中培养长达2周。将培养基和从细胞中提取的物质在Sephacryl S - 200柱上进行凝胶过滤色谱,以分离蛋白质。使用时间分辨荧光免疫测定法和放射免疫测定法对各组分进行酸性和中性半胱氨酸蛋白酶抑制剂(ACPI、NCPI)检测,并使用木瓜蛋白酶测定半胱氨酸蛋白酶抑制活性。游离的NCPI,即一种在pH 6.0和6.5具有等电变体的分子,其Mr约为12000且能够抑制木瓜蛋白酶,在培养基和细胞中均被检测到。免疫扩散研究揭示了它与源自人脾脏的NCPI具有免疫学同一性。在培养期间NCPI的量增加。ACPI被表征为一种等电点为4.9、Mr约为12000、具有木瓜蛋白酶抑制能力且与源自脾脏的ACPI具有抗原反应性的分子,在培养基中未检测到。然而,在培养2周后的细胞中检测到了它。这些数据证明在当前培养条件下,ACPI和NCPI由NCTC - 2544细胞合成。

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