Tapanainen J S, Tilly J L, Vihko K K, Hsueh A J
Department of Gynecology and Obstetrics, Stanford University School of Medicine, California 94305-5317.
Mol Endocrinol. 1993 May;7(5):643-50. doi: 10.1210/mend.7.5.8316250.
Although the requirement for pituitary gonadotropins during testicular cell differentiation is well documented, the possible role of FSH and LH in regulating testicular cell survival has not been studied. Using a quantitative autoradiographic method for the detection of internucleosomal DNA fragmentation, a hallmark feature of apoptosis, the hormonal control of apoptotic cell death was studied in testicular cells collected from immature rats after hypophysectomy. After surgery, animals were treated with daily injections of 20 IU long-acting FSH agonist (FSH-CTP) or 50 IU human CG (hCG) for 2 days. Hypophysectomy decreased testis weight by 25%, but treatment with FSH-CTP or hCG prevented the effect of hypophysectomy. Testes of intact animals contained predominantly high-mol wt DNA, whereas hypophysectomy increased DNA cleavage into low-mol wt (< 15 kilobases) ladders characteristics of apoptosis. In contrast, treatment with FSH-CTP or hCG inhibited hypophysectomy-induced apoptotic DNA cleavage by 84% and 51%, respectively. Hypophysectomy-induced DNA fragmentation was found in both interstitial cells and seminiferous tubules. Similar to whole testis, treatment with FSH-CTP suppressed hypophysectomy-induced apoptosis by over 90% in seminiferous tubules and interstitial cells. In contrast, hCG treatment was less effective in preventing hypophysectomy-induced DNA cleavage (46% suppression in tubules and 77% suppression in interstitial cells). Furthermore, testosterone replacement also suppressed hypophysectomy-induced DNA fragmentation by 75% in the whole testis tissue, 64% in tubules, and 55% in interstitial cells. To further study the role of gonadotropins, intact animals were treated with a potent GnRH antagonist (Azaline B, 10 microgram/day) to decrease serum gonadotropin levels.(ABSTRACT TRUNCATED AT 250 WORDS)
尽管睾丸细胞分化过程中对垂体促性腺激素的需求已有充分记录,但促卵泡激素(FSH)和促黄体生成素(LH)在调节睾丸细胞存活方面的潜在作用尚未得到研究。利用定量放射自显影法检测核小体间DNA片段化(凋亡的一个标志性特征),对垂体切除术后未成熟大鼠睾丸细胞中凋亡细胞死亡的激素调控进行了研究。手术后,动物每天注射20国际单位长效FSH激动剂(FSH - CTP)或50国际单位人绒毛膜促性腺激素(hCG),持续2天。垂体切除术使睾丸重量减少25%,但用FSH - CTP或hCG治疗可防止垂体切除术的这种影响。完整动物的睾丸主要含有高分子量DNA,而垂体切除术则增加了DNA切割为凋亡特征性的低分子量(<15千碱基)梯状条带。相反,用FSH - CTP或hCG治疗分别抑制了垂体切除术诱导的凋亡DNA切割的84%和51%。在间质细胞和生精小管中均发现了垂体切除术诱导的DNA片段化。与整个睾丸相似,用FSH - CTP治疗在生精小管和间质细胞中抑制垂体切除术诱导凋亡超过90%。相比之下,hCG治疗在防止垂体切除术诱导的DNA切割方面效果较差(在小管中抑制46%,在间质细胞中抑制77%)。此外,睾酮替代也分别在整个睾丸组织中抑制垂体切除术诱导的DNA片段化75%,在小管中抑制64%,在间质细胞中抑制55%。为进一步研究促性腺激素的作用,对完整动物用强效促性腺激素释放激素(GnRH)拮抗剂(阿扎林B,10微克/天)治疗以降低血清促性腺激素水平。(摘要截选至250字)