Kulkarni S, Shethna Y I
Department of Life Sciences, University of Bombay.
Indian J Med Res. 1992 Aug;96:236-44.
Angiogenic factors were isolated by ion exchange chromatography from three established cell lines viz., HEp 2, HeLa and CHO, a primary culture of mouse mammary adenocarcinoma and from conditioned media of HEp2 and cultured mammary adenocarcinoma cells. The angiogenic activity was assayed by chicken chorioallantoic membrane assay. The angiogenic factor eluted at 0.5 M, exhibited lambda max at 258 +/- 1 nm, contained protein and nucleic acid. The cellular angiogenic factor showed a ratio of 1:1 for protein and nucleic acid whereas the secreted angiogenic factor had 3-5 parts of protein to 1 part of nucleic acid. The angiogenic factor from HEp2 and CHO cells did not bind to heparin-agarose. Microheterogeneity of the angiogenic factors was established by SDS-PAGE. Antiserum raised against the cellular angiogenic factor from HEp2 cells, showed a titre of 1:1600 by ELISA. The angiogenic factor was directly localized on whole cells by ELISA. Cellular as well as secreted angiogenic factors crossreacted with the antibody. Neutralizing effect of the antiserum on induction of angiogenesis was detected on chicken chorioallantoic membrane.
通过离子交换色谱法从三种已建立的细胞系(即HEp 2、HeLa和CHO)、小鼠乳腺腺癌原代培养物以及HEp2和培养的乳腺腺癌细胞的条件培养基中分离出血管生成因子。通过鸡胚绒毛尿囊膜试验测定血管生成活性。在0.5M处洗脱的血管生成因子,在258±1nm处有最大吸收峰,含有蛋白质和核酸。细胞血管生成因子的蛋白质与核酸比例为1:1,而分泌的血管生成因子的蛋白质与核酸比例为3 - 5:1。来自HEp2和CHO细胞的血管生成因子不与肝素 - 琼脂糖结合。通过SDS - PAGE确定了血管生成因子的微异质性。用抗HEp2细胞的细胞血管生成因子制备的抗血清,通过ELISA显示效价为1:1600。通过ELISA将血管生成因子直接定位在全细胞上。细胞和分泌的血管生成因子都与抗体发生交叉反应。在鸡胚绒毛尿囊膜上检测到抗血清对血管生成诱导的中和作用。