Woods K L, Porter T E
Department of Poultry Science, Institute for Biosciences and Technology, College Station, Texas, 77843-2472, USA.
Gen Comp Endocrinol. 1998 Nov;112(2):240-6. doi: 10.1006/gcen.1998.7168.
It was previously reported that prolactin (PRL)-containing cells differentiate by days 15 to 19 of embryonic development and that vasoactive intestinal peptide (VIP) increased plasma PRL concentrations and pituitary PRL protein and mRNA levels in vivo. In the present study, anterior pituitaries derived from day 15, 16, 17, 18, and 19 embryos were subjected to reverse hemolytic plaque assays (RHPA) for chicken PRL to determine the ontogeny of lactotrophs. We found that PRL secreting cells were first consistently detected on day 17 of embryonic development, indicating that lactotroph differentiation during normal development occurs by this age. However, extended treatment in the RHPA with VIP exposed lactotrophs as early as day 15, suggesting that a lactotroph precursor population was present earlier. Next, primary cultures of embryonic anterior pituitary cells from day 12, 13, 14, 15, 16, and 17 embryos were incubated for 0, 2, or 4 days in serum-free medium or medium supplemented with 10 nM VIP. After the culture periods, cells were subjected to RHPAs for chicken PRL. PRL-secreting cells differentiated spontaneously by 2 days in culture for day 15 and 16 cells and by 4 days in culture for all embryonic ages tested, except day 17. Culturing with VIP for 2 days did not increase PRL-secreting cells at any embryonic age tested, whereas VIP treatment for 4 days increased lactotroph numbers at all ages except day 12. Cells from days 15, 16, and 17 were responsive to VIP in the RHPA after 2 days in untreated cultures, but after 4 days only day 17 cells continued to respond to VIP in the RHPA. Treatment with VIP in culture for 4 days maintained VIP responsiveness in the RHPA for cells derived from embryos as early as day 14. We conclude that lactotroph differentiation during normal chicken development occurs by embryonic day 17. Moreover, our results indicate that responsiveness to VIP is an early event in PRL cell development and that lactotroph differentiation may be stimulated in vitro by VIP as early as embryonic day 13.
先前有报道称,含催乳素(PRL)的细胞在胚胎发育的第15至19天分化,并且血管活性肠肽(VIP)在体内可提高血浆PRL浓度以及垂体PRL蛋白和mRNA水平。在本研究中,对来自第15、16、17、18和19天胚胎的垂体前叶进行鸡PRL的反向溶血空斑试验(RHPA),以确定催乳素细胞的个体发生。我们发现,在胚胎发育的第17天首次持续检测到分泌PRL的细胞,这表明在正常发育过程中催乳素细胞的分化在这个年龄发生。然而,在RHPA中用VIP进行延长处理早在第15天就暴露了催乳素细胞,这表明更早存在催乳素细胞前体群体。接下来,将来自第12、13、14、15、16和17天胚胎的垂体前叶细胞原代培养物在无血清培养基或补充有10 nM VIP的培养基中培养0、2或4天。培养期结束后,对细胞进行鸡PRL的RHPA检测。对于第15和16天的细胞,分泌PRL的细胞在培养2天后自发分化,对于除第17天外的所有测试胚胎年龄,在培养4天后自发分化。在任何测试的胚胎年龄,用VIP培养2天均未增加分泌PRL的细胞,而VIP处理4天在除第12天外的所有年龄均增加了催乳素细胞数量。在未处理的培养物中培养2天后,来自第15、16和17天的细胞在RHPA中对VIP有反应,但在4天后只有第17天的细胞在RHPA中继续对VIP有反应。在培养中用VIP处理4天可维持早在第14天胚胎来源的细胞在RHPA中对VIP的反应性。我们得出结论,在正常鸡的发育过程中,催乳素细胞的分化在胚胎第17天发生。此外,我们的结果表明,对VIP的反应性是PRL细胞发育中的早期事件,并且早在胚胎第13天,VIP在体外可能刺激催乳素细胞分化。