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培养的人皮肤成纤维细胞中,干扰素γ对从头蛋白质合成的调节具有解剖学部位依赖性。

Interferon gamma regulation of de novo protein synthesis in human dermal fibroblasts in culture is anatomic site dependent.

作者信息

Smith T J, Higgins P J

机构信息

Department of Medicine, Albany Medical College, NY 12208.

出版信息

J Invest Dermatol. 1993 Mar;100(3):288-92. doi: 10.1111/1523-1747.ep12469828.

Abstract

The propensity of the skin of the lower anterior leg to be involved in Graves' dermopathy prompted an examination of the specific protein synthesis and response to interferon gamma in cultured fibroblasts from this area. Confluent cultures from normal skin of the lower leg and from the abdomen of the same three donors were pulse labeled with [35S]methionine for 3 h and subjected to two-dimensional protein gel electrophoresis and fluorography. Protein spots were mapped using a computer-driven program and the relative densities of the resolvable spots analyzed. Fibroblasts from the two anatomic sites display distinct patterns of de novo protein synthesis. Of the 157 abundant spots arbitrarily chosen for analysis, 31% varied substantially in levels of expression between the sites. A number of proteins appear to be expressed only in cultures derived from one of the two anatomic sites. Interferon gamma (100 U/ml) present in the culture medium for 48 h influenced the abundance of a number of proteins in a site-specific manner. Among them, plasminogen activator inhibitor type-1 was induced three to five times in the leg cultures, whereas this same polypeptide was down-regulated in abdominal fibroblasts. A 54-kD protein was induced in interferon-treated cultures from both sites at least 50 times. It appears that fibroblasts from different regions of the integument are intrinsically distinct in terms of both their protein synthetic programs and their responses to cytokines.

摘要

小腿前侧下部皮肤易患格雷夫斯病皮肤病变,这促使人们对该区域培养的成纤维细胞中的特定蛋白质合成及对干扰素γ的反应进行研究。来自相同三名供体的小腿正常皮肤和腹部皮肤的汇合培养物用[35S]甲硫氨酸脉冲标记3小时,然后进行二维蛋白质凝胶电泳和荧光自显影。使用计算机驱动程序对蛋白质斑点进行定位,并分析可分辨斑点的相对密度。来自这两个解剖部位的成纤维细胞表现出不同的从头蛋白质合成模式。在随机选择进行分析的157个丰富斑点中,31%在两个部位之间的表达水平有很大差异。一些蛋白质似乎仅在来自两个解剖部位之一的培养物中表达。培养基中存在48小时的干扰素γ(100 U/ml)以位点特异性方式影响了许多蛋白质的丰度。其中,纤溶酶原激活物抑制剂1型在腿部培养物中被诱导三到五倍,而在腹部成纤维细胞中该相同多肽被下调。一种54-kD的蛋白质在两个部位经干扰素处理的培养物中至少被诱导50倍。看来,来自体表不同区域的成纤维细胞在其蛋白质合成程序和对细胞因子的反应方面本质上是不同的。

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