Grazul-Bilska A T, Reynolds L P, Slanger W D, Redmer D A
Department of Animal and Range Sciences, North Dakota State University, Fargo 58105.
J Anim Sci. 1992 Jan;70(1):254-62. doi: 10.2527/1992.701254x.
Effects of luteal-conditioned media (LCM) on proliferation and migration of endothelial cells were used to assess angiogenic activity of corpora lutea (CL) obtained from cows on d 100 (n = 5), 150 (n = 6), 200 (n = 6), and 250 (n = 6) of gestation. Explants of CL (200 mg) were incubated for 6 h in 3 mL of serum-free media containing no hormone, LH (1 microgram/mL), prostaglandin F2 alpha (PGF2 alpha; 3 microM), or both hormones. Media from the four stages of gestation were subjected to the following procedures: 1) ultrafiltration, 2) high-salt (3.0 M NaCl) treatment and then ultrafiltration, 3) heat treatment, 4) heparin-Sepharose affinity chromatography, 5) immunoneutralization with specific antibodies against heparin-binding growth factor (HBGF)-1 and against HBGF-2, and 6) dot immunoblot assay for HBGF-2. Fractions from the first five procedures were evaluated in the endothelial cell proliferation bioassay. In addition, progesterone concentration of LCM was determined by RIA. Across all days of gestation and hormone treatments, LCM stimulated (P less than .05) proliferation and migration of endothelial cells, but activities did not differ among stages of gestation or hormone treatments. Both mitogenic and migration-stimulating fractions seemed to have Mr greater than 100,000. The mitogenic activity fraction had an apparent Mr greater than 100,000 even after treatment with high salt and was heat-labile. This endothelial mitogen was retained on heparin-Sepharose columns and was eluted with 2.0 M NaCl. Mitogenic activity was partly neutralized (P less than .05) by antibodies against HBGF-2 but not HBGF-1. Presence of HBGF-2 in LCM was detected by dot immunoblot assay.(ABSTRACT TRUNCATED AT 250 WORDS)
采用黄体条件培养基(LCM)对内皮细胞增殖和迁移的影响,来评估妊娠第100天(n = 5)、150天(n = 6)、200天(n = 6)和250天(n = 6)的奶牛黄体(CL)的血管生成活性。将CL组织块(200 mg)在不含激素、含促黄体素(LH,1微克/毫升)、前列腺素F2α(PGF2α,3微摩尔)或两种激素的3毫升无血清培养基中孵育6小时。来自妊娠四个阶段的培养基进行以下处理:1)超滤;2)高盐(3.0 M NaCl)处理然后超滤;3)热处理;4)肝素-琼脂糖亲和层析;5)用抗肝素结合生长因子(HBGF)-1和抗HBGF-2的特异性抗体进行免疫中和;6)对HBGF-2进行斑点免疫印迹分析。前五个步骤得到的组分在内皮细胞增殖生物测定中进行评估。此外,通过放射免疫分析法测定LCM中的孕酮浓度。在所有妊娠天数和激素处理中,LCM均刺激(P <.05)内皮细胞的增殖和迁移,但不同妊娠阶段或激素处理之间的活性无差异。促有丝分裂和迁移刺激组分的分子量似乎均大于100,000。即使经过高盐处理,促有丝分裂活性组分的表观分子量仍大于100,000,且对热不稳定。这种内皮有丝分裂原保留在肝素-琼脂糖柱上,并用2.0 M NaCl洗脱。抗HBGF-2抗体可部分中和(P <.05)促有丝分裂活性,但抗HBGF-1抗体则不能。通过斑点免疫印迹分析检测到LCM中存在HBGF-2。(摘要截短至250字)