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从下丘脑对角质形成细胞生长因子进行表征及部分纯化。

Characterization and partial purification of keratinocyte growth factor from the hypothalamus.

作者信息

Gilchrest B A, Marshall W L, Karassik R L, Weinstein R, Maciag T

出版信息

J Cell Physiol. 1984 Sep;120(3):377-83. doi: 10.1002/jcp.1041200316.

Abstract

An extract of bovine hypothalamus is known to be mitogenic for human keratinocytes in vitro. In order to identify the responsible substance(s), biochemical characterization and subsequent bioassay of the extract in a serum-free culture system were performed. The keratinocyte growth-promoting activity of the hypothalamic extract was unaffected by heating (100 degrees C, 10 min); acidification to pH 3.3; or by exposure to lipase, RNAase, or proteolytic enzymes; but was abolished by alkalinization to pH 11. An approximate molecular weight of 1,700 daltons was determined by elution on a calibrated Sephadex G-25 column, and an approximate pl of 3.5 was determined by isoelectric focusing. Optimal concentrations of the crude extract (150-300 micrograms/ml) increased keratinocyte growth approximately 50-fold compared to control cultures lacking the extract. Partial purification resulted in a preparation biologically active at 30 ng/ml protein equivalent and was consistent with the presence of a single mitogen which we have termed keratinocyte growth factor (KGF). Mitogenic activity for human melanocytes, dermal fibroblasts, and endothelial cells, present in the crude hypothalamic extract, was lacking in heat-treated preparations that contained KGF. Optimal concentrations of purified epidermal growth factor and ethanolamine, the only remotely similar substances previously reported to augment keratinocyte growth in vitro, could not substitute for KGF in the serum-free culture system. Keratinocyte growth-promoting activity comparable to that observed in bovine hypothalamic extracts was present in human hypothalamic extracts prepared in the same manner.

摘要

已知牛下丘脑提取物在体外对人角质形成细胞有促有丝分裂作用。为了鉴定其中的活性物质,我们在无血清培养系统中对该提取物进行了生化特性分析及后续生物测定。下丘脑提取物对角质形成细胞的生长促进活性不受加热(100℃,10分钟)、酸化至pH 3.3或暴露于脂肪酶、RNA酶或蛋白水解酶的影响,但在碱化至pH 11时被消除。通过在经校准的Sephadex G - 25柱上洗脱测定其近似分子量为1700道尔顿,通过等电聚焦测定其近似pI为3.5。与不含该提取物的对照培养物相比,粗提取物的最佳浓度(150 - 300微克/毫升)可使角质形成细胞生长增加约50倍。部分纯化得到一种在相当于30纳克/毫升蛋白质时具有生物活性的制剂,这与存在一种单一的有丝分裂原一致,我们将其称为角质形成细胞生长因子(KGF)。粗下丘脑提取物中存在的对人黑素细胞、真皮成纤维细胞和内皮细胞的促有丝分裂活性在含有KGF的热处理制剂中不存在。纯化的表皮生长因子和乙醇胺(以前报道的仅有的在体外可增强角质形成细胞生长的类似物质)的最佳浓度在无血清培养系统中不能替代KGF。以相同方式制备的人下丘脑提取物中存在与牛下丘脑提取物中观察到的类似的角质形成细胞生长促进活性。

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