Nagasaka M, Yasumizu T, Nagasaka H, Kato J
Department of Obstetrics and Gynecology, Yamanashi Medical College.
Nihon Sanka Fujinka Gakkai Zasshi. 1992 Mar;44(3):329-35.
The purpose of this study is to develop an assay system for quantification of bFGF in human tissue and to investigate the changes in bFGF content in the human placenta during pregnancy. Sixty-two placental tissue samples from various stages of normal pregnancies were collected. Approximately 28 micrograms bFGF was obtained per 1 kg of placental tissue. The recovery rates were 17.1 +/- 7.4%. The purified samples were confirmed as bFGF by SDS-PAGE and enzyme-linked immunoelectrotransfer blot (EITB) with anti-human bFGF monoclonal antibody. The bFGF readings in the human placenta determined by RIA were 11.81 +/- 2.11 fmol/mg protein (first trimester), 20.45 +/- 4.85 (early second trimester), 9.52 +/- 5.02 (late second trimester), 7.41 +/- 2.07 (third trimester), and 7.75 +/- 1.86 (post trimester). The placental bFGF were significantly high in the early stage of second trimester and declined gradually during the remainder of the pregnancy. The RIA values were correlated closely with the values obtained by bioassay. These results demonstrate that our assay system provides a tool for the quantification of bFGF in biological samples and suggest that bFGF, the active mitogen and angiogenic factor, participates in the formation of the human placenta.
本研究的目的是开发一种用于定量人体组织中碱性成纤维细胞生长因子(bFGF)的检测系统,并研究孕期人胎盘组织中bFGF含量的变化。收集了62份来自正常孕期不同阶段的胎盘组织样本。每1千克胎盘组织约获得28微克bFGF。回收率为17.1±7.4%。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和用抗人bFGF单克隆抗体进行的酶联免疫电转移印迹(EITB),确认纯化后的样本为bFGF。通过放射免疫分析(RIA)测定,人胎盘组织中的bFGF读数为:孕早期11.81±2.11飞摩尔/毫克蛋白,孕中期早期20.45±4.85,孕中期晚期9.52±5.02,孕晚期7.41±2.07,产后7.75±1.86。胎盘bFGF在孕中期早期显著升高,在孕期其余阶段逐渐下降。RIA值与生物测定法得到的值密切相关。这些结果表明,我们的检测系统为定量生物样本中的bFGF提供了一种工具,并提示bFGF这种活性促有丝分裂原和血管生成因子参与了人胎盘的形成。