May J V, Bridge A J, Gotcher E D, Gangrade B K
Department of Obstetrics and Gynecology, University of Kansas School of Medicine, Wichita.
Endocrinology. 1992 Aug;131(2):689-97. doi: 10.1210/endo.131.2.1639016.
An important but poorly understood aspect of mammalian follicle development involves the regulation of theca cell proliferation. To investigate the premise that growth factors regulate theca cell proliferation, porcine theca cells were prepared by collagenase/DN'ase digestion of follicle linings after the removal of the granulosa cells and allowed to attach for 24 h. This method provided a monolayer of theca cells that had little if any granulosa cell contamination and which secreted high levels of androstenedione relative to granulosa cells during moderate-term culture (33-fold difference, P less than 0.01). In medium containing fetal calf serum (10%), theca cells were significantly more responsive to platelet-derived growth factor (PDGF) than epidermal growth factor (EGF) in terms of proliferation (13.4 +/- 0.2-vs. 7.0 +/- 0.1-fold increases relative to the initial cell count, P less than 0.05). This is in contrast to granulosa cells which were significantly more responsive to EGF than PDGF (7.1 +/- 0.1 vs. 4.0 +/- 0.2 fold-increases, P less than 0.05). Since serum has been shown to contain both EGF and PDGF, proliferation studies were performed using plasma-derived serum (PDS) which is growth factor restricted to examine more closely the direct effects of growth factors. In medium containing 0.25% PDS and within experiments, PDGF (1-25 ng/ml) stimulated theca cell proliferation in a dose-dependent manner (2.3-fold increase relative to controls, P less than 0.05) whereas EGF did not. EGF, however, markedly enhanced the proliferative action of PDGF (6.4-fold increase relative to controls, P less than 0.05). Insulin-like growth factor I and low density lipoprotein, factors which enhance markedly the proliferative effects of EGF and PDGF in terms of granulosa cell proliferation, exhibited only a modest synergistic effect with respect to EGF and PDGF upon theca cells (9.5-fold increase vs. a 6.4-fold increase above controls, P less than 0.05). Temporal studies in vitro indicate that theca cell proliferation is low during the first 3-day exposure to growth factors irrespective of treatment (a 2-fold increase over the seeding density). During the second 3-day exposure, however, theca cell proliferation increases 4- to 5-fold. The temporal pattern of theca cell proliferation stimulated by fetal calf serum supplemented with EGF or PDGF and PDS-containing medium supplemented with PDGF, EGF, insulin-like growth factor I, and low density lipoprotein is similar. These results suggest that PDGF is a major mitogen toward porcine theca cells and that EGF greatly enhances its activity.(ABSTRACT TRUNCATED AT 400 WORDS)
哺乳动物卵泡发育中一个重要但尚未得到充分理解的方面涉及卵泡膜细胞增殖的调控。为了研究生长因子调节卵泡膜细胞增殖这一前提,在去除颗粒细胞后,通过胶原酶/脱氧核糖核酸酶消化卵泡内膜制备猪卵泡膜细胞,并使其贴壁24小时。该方法提供了单层卵泡膜细胞,几乎没有颗粒细胞污染,并且在中期培养(33倍差异,P小于0.01)期间,相对于颗粒细胞,其分泌高水平的雄烯二酮。在含有胎牛血清(10%)的培养基中,就增殖而言,卵泡膜细胞对血小板衍生生长因子(PDGF)的反应明显比对表皮生长因子(EGF)更敏感(相对于初始细胞计数增加13.4±0.2倍对7.0±0.1倍,P小于0.05)。这与颗粒细胞形成对比,颗粒细胞对EGF的反应明显比对PDGF更敏感(7.1±0.1倍对4.0±0.2倍增加,P小于0.05)。由于已证明血清中同时含有EGF和PDGF,因此使用生长因子受限的血浆衍生血清(PDS)进行增殖研究,以更密切地检查生长因子的直接作用。在含有0.25%PDS的培养基中且在实验范围内,PDGF(1 - 25 ng/ml)以剂量依赖方式刺激卵泡膜细胞增殖(相对于对照增加2.3倍,P小于0.05),而EGF则无此作用。然而,EGF显著增强了PDGF的增殖作用(相对于对照增加6.4倍,P小于0.05)。胰岛素样生长因子I和低密度脂蛋白,这些因子在颗粒细胞增殖方面显著增强EGF和PDGF的增殖作用,但对卵泡膜细胞而言,它们与EGF和PDGF仅表现出适度的协同作用(相对于对照增加9.5倍对6.4倍增加,P小于0.05)。体外时间研究表明,无论处理如何,在最初3天暴露于生长因子期间,卵泡膜细胞增殖较低(比接种密度增加2倍)。然而,在接下来的3天暴露期间,卵泡膜细胞增殖增加4至5倍。补充有EGF或PDGF的胎牛血清以及补充有PDGF、EGF、胰岛素样生长因子I和低密度脂蛋白的含PDS培养基所刺激的卵泡膜细胞增殖的时间模式相似。这些结果表明,PDGF是猪卵泡膜细胞的主要促有丝分裂原,并且EGF极大地增强了其活性。(摘要截短至400字)