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大鼠血清中生长激素依赖性生长调节素结合蛋白的进一步特性鉴定以及培养的大鼠肝细胞产生的生长调节素结合蛋白的证明。

Further characterization of growth hormone-dependent somatomedin-binding proteins in rat serum and demonstration of somatomedin-binding proteins produced by rat liver cells in culture.

作者信息

Moses A C, Nissley S P, Passamani J, White R M

出版信息

Endocrinology. 1979 Feb;104(2):536-46. doi: 10.1210/endo-104-2-536.

Abstract

The somatomedin-like peptide multiplication-stimulating activity (MSA) binds specifically to rat serum. The pattern of MSA binding is GH dependent. Specific binding of [125I]iodo-MSA in normal rat serum is primarily in the gamma-globulin region (peak II) on Sephadex G-200, while MSA binding in hypophysectomized (hypox) rat serum is near the albumin region (peak III). This study further characterizes the peak II and peak III somatomedin-binding proteins produced by rat liver cells in culture. [125I]Iodo-MSA binding to normal rat serum is abolished by trypsin pretreatment of rat serum, suggesting that MSA binds to protein components of serum. The only detectable somatomedin activity (measured by [3H]thymidine incorporation into chick embryo fibroblast DNA) in fractions of normal rat serum chromatographed on Sephadex G-200 coincides with peak II binding of [125I]iodo-MSA. In hypox rat serum, the majority of detectable somatomedin activity is in the peak III region. There is complete displacement of the human somatomedins [125I]iodoinsulin-like growth factor I and II and [125I]iodosomatomedin A from the rat serum-binding sites by unlabeled MSA, suggesting that the human somatomedins bind to the same sites as MSA. Treatment of normal rat serum with 1 M acetic acid dissociates somatomedin activity from its binding proteins and converts somatomedin-binding proteins from peak II to peak III. Scatchard analysis of competitive binding data using [125I]iodo-MSA yields a binding affinity that is not appreciably different for either normal or hypox rat sera. The binding capacity of normal or acid-treated normal rat serum for MSA is significantly greater than that for comparably treated hypox rat sera. Although the site of synthesis of somatomedin-binding proteins in vivo is unknown, specific somatomedin-binding proteins are synthesized by two rat liver cell lines in culture. These rat liver cell somatomedin-binding proteins have the same molecular size and the same binding affinity for MSA as the peak III somatomedin-binding protein(s) in rat serum.

摘要

类生长调节素样肽增殖刺激活性(MSA)与大鼠血清特异性结合。MSA的结合模式依赖于生长激素(GH)。正常大鼠血清中[125I]碘代-MSA的特异性结合主要位于Sephadex G - 200上的γ-球蛋白区域(峰II),而垂体切除(hypox)大鼠血清中的MSA结合则靠近白蛋白区域(峰III)。本研究进一步对培养的大鼠肝细胞产生的峰II和峰III生长调节素结合蛋白进行了表征。用胰蛋白酶预处理大鼠血清可消除[125I]碘代-MSA与正常大鼠血清的结合,这表明MSA与血清中的蛋白质成分结合。在Sephadex G - 200上进行层析的正常大鼠血清组分中,唯一可检测到的生长调节素活性(通过[3H]胸腺嘧啶掺入鸡胚成纤维细胞DNA来测量)与[125I]碘代-MSA的峰II结合一致。在hypox大鼠血清中,则大部分可检测到的生长调节素活性位于峰III区域。未标记的MSA可完全取代大鼠血清结合位点上的人生长调节素[125I]碘胰岛素样生长因子I和II以及[125I]碘生长调节素A,这表明人生长调节素与MSA结合于相同位点。用1 M乙酸处理正常大鼠血清可使生长调节素活性与其结合蛋白解离,并将生长调节素结合蛋白从峰II转变为峰III。使用[125I]碘代-MSA对竞争结合数据进行Scatchard分析得出的结合亲和力,对于正常或hypox大鼠血清而言并无明显差异。正常或经酸处理的正常大鼠血清对MSA的结合能力显著大于经类似处理的hypox大鼠血清。虽然体内生长调节素结合蛋白的合成位点尚不清楚,但培养的两种大鼠肝细胞系可合成特异性的生长调节素结合蛋白。这些大鼠肝细胞生长调节素结合蛋白与大鼠血清中的峰III生长调节素结合蛋白具有相同的分子大小和对MSA相同的结合亲和力。

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