Burger L L, Sherwood O D
Department of Molecular in Integrative Physiology, University of Illinois at Urbana-Champaign, Urbana 61801, USA.
Endocrinology. 1998 Sep;139(9):3984-95. doi: 10.1210/endo.139.9.6210.
Both cervical and vaginal growth are relaxin dependent during rat pregnancy. We recently reported a relaxin-dependent 1.5-fold increase in cervical and vaginal DNA content from midpregnancy until term. This finding indicated that relaxin probably promotes cervical and vaginal growth at least in part by promoting cellular proliferation. The objective of this study was to identify and quantify cells in the cervix and vagina that proliferate during the second half of rat pregnancy in response to relaxin. Primiparous pregnant rats were ovariectomized or sham ovariectomized (group C; n = 8) on day 9 of pregnancy (D9). Ovariectomized rats were then treated with physiological doses of progesterone plus estrogen (n = 7) or progesterone, estrogen, and porcine relaxin (n = 7). Cellular proliferation was determined by continuously administering a low dose of 5-bromo-2'-deoxyuridine (BrdU) via miniature osmotic pump from D9-D22. On D22, cervices and vaginas were collected, fixed in formalin, paraffin embedded, and serially sectioned (4 microm). Adjacent serial sections were either immunostained for BrdU to assess cell proliferation or stained with hematoxylin to determine total cell number. Cell proliferation was evaluated by counting BrdU-positive nuclei and total nuclei in the same area on adjacent sections. Cell counts were determined using computerized digital morphometric analysis at x575. In control rats, nearly 75% of the epithelial cells and 55% of the stromal cells within the cervix at term had proliferated during the second half of pregnancy. The accumulation of approximately half of the new cells was relaxin dependent. Within the cervical stroma, relaxin increased the accumulation of cells associated with blood vessels and also the number of isolated cells (probably fibroblasts). Relaxin did not appear to affect smooth muscle cell proliferation in the cervix. In contrast to the cervix, a minority of vaginal epithelial cells (45%) and stromal cells (20%) proliferated during the second half of pregnancy. Although relaxin appeared to have a tendency to increase the accumulation of new vaginal epithelial and stromal cells, morphometric analysis did not provide support for such an effect. In conclusion, this study demonstrates that relaxin promotes a marked increase in the accumulation of new epithelial cells and stromal cells within the cervix. The relaxin-induced increase in new epithelial and stromal cells probably contributes to relaxin's effects on growth and remodeling of the cervix that are required for rapid and safe delivery.
在大鼠妊娠期间,宫颈和阴道的生长均依赖松弛素。我们最近报道,从妊娠中期到足月,宫颈和阴道的DNA含量在松弛素的作用下增加了1.5倍。这一发现表明,松弛素可能至少部分通过促进细胞增殖来促进宫颈和阴道的生长。本研究的目的是识别和量化大鼠妊娠后半期宫颈和阴道中因松弛素而增殖的细胞。在妊娠第9天(D9),将初产妊娠大鼠进行卵巢切除或假卵巢切除(C组;n = 8)。然后,对卵巢切除的大鼠给予生理剂量的孕酮加雌激素(n = 7)或孕酮、雌激素和猪松弛素(n = 7)。通过从D9至D22经由微型渗透泵持续给予低剂量的5-溴-2'-脱氧尿苷(BrdU)来测定细胞增殖。在D22,收集宫颈和阴道,用福尔马林固定,石蜡包埋,并连续切片(4微米)。相邻的连续切片要么进行BrdU免疫染色以评估细胞增殖,要么用苏木精染色以确定总细胞数。通过计数相邻切片同一区域的BrdU阳性细胞核和总细胞核来评估细胞增殖。使用计算机化数字形态计量分析在x575下确定细胞计数。在对照大鼠中,足月时宫颈内近75%的上皮细胞和55%的基质细胞在妊娠后半期发生了增殖。大约一半新细胞的积累依赖于松弛素。在宫颈基质内,松弛素增加了与血管相关的细胞积累以及孤立细胞(可能是成纤维细胞)的数量。松弛素似乎不影响宫颈平滑肌细胞的增殖。与宫颈不同,在妊娠后半期,少数阴道上皮细胞(45%)和基质细胞(20%)发生了增殖。尽管松弛素似乎有增加新的阴道上皮和基质细胞积累的趋势,但形态计量分析并未支持这种作用。总之,本研究表明,松弛素促进宫颈内新上皮细胞和基质细胞积累的显著增加。松弛素诱导的新上皮和基质细胞增加可能有助于松弛素对宫颈生长和重塑的作用,而这对于快速安全分娩是必需的。