Buchanan L J, Riches A C
Prostate. 1986;8(1):63-74. doi: 10.1002/pros.2990080108.
Effects of variations in organ culture media and methodology on the proliferative activity of rat ventral prostate and its response to testosterone were investigated quantitatively by using the incorporation of [125I]-iododeoxyuridine (125I-UdR) to monitor DNA synthesis. In serum-free medium, maximal increases in DNA synthesis occurred when testosterone was introduced during the first 48 hours of the culture. Supplementation of the medium with 5% fetal calf serum did not alter the responses in control or testosterone-treated cultures, whereas the addition of insulin (3 micrograms/ml) alone or in combination with serum promoted cell proliferation in testosterone-free cultures and enhanced the stimulatory effect of testosterone. Unlike grid-supported cultures, suspension cultures of rat ventral prostate exhibited increased proliferative activity both in the presence and absence of testosterone. Thus, variations in experimental procedure may account for differences in the proliferative activity of rat prostate between organ culture studies.
通过掺入[125I]-碘脱氧尿苷(125I-UdR)来监测DNA合成,定量研究了器官培养基和方法的变化对大鼠腹侧前列腺增殖活性及其对睾酮反应的影响。在无血清培养基中,当在培养的最初48小时内加入睾酮时,DNA合成出现最大增加。向培养基中添加5%胎牛血清不会改变对照或睾酮处理培养物中的反应,而单独添加胰岛素(3微克/毫升)或与血清联合添加可促进无睾酮培养物中的细胞增殖,并增强睾酮的刺激作用。与网格支持培养不同,大鼠腹侧前列腺的悬浮培养在有和没有睾酮的情况下均表现出增殖活性增加。因此,实验程序的变化可能解释了器官培养研究之间大鼠前列腺增殖活性的差异。