Ackert C L, Gittens J E, O'Brien M J, Eppig J J, Kidder G M
Department of Physiology, The University of Western Ontario, London, Ontario N6A 5C1, Canada.
Dev Biol. 2001 May 15;233(2):258-70. doi: 10.1006/dbio.2001.0216.
The ovarian follicle in mammals is a functional syncytium, with the oocyte being coupled with the surrounding cumulus granulosa cells, and the cumulus cells being coupled with each other and with the mural granulosa cells, via gap junctions. The gap junctions coupling granulosa cells in mature follicles contain several different connexins (gap junction channel proteins), including connexins 32, 43, and 45. Connexin43 immunoreactivity can be detected from the onset of folliculogenesis just after birth and persists through ovulation. In order to assess the importance of connexin43 gap junctions for postnatal folliculogenesis, we grafted ovaries from late gestation mouse fetuses or newborn pups lacking connexin43 (Gja1(-)/Gja1(-)) into the kidney capsules of adult females and allowed them to develop for up to 3 weeks (this was necessitated by the neonatal lethality caused by the mutation). By the end of the graft period, tertiary (antral) follicles had developed in grafted normal (wild-type or heterozygote) ovaries. Most follicles in Gja1(-)/Gja1(-) ovaries, however, failed to become multilaminar, with the severity of the effect depending on strain background. Dye transfer experiments indicated that intercellular coupling between granulosa cells is reduced, but not abolished, in the absence of connexin43, consistent with the presence of additional connexins. These results suggest that coupling between granulosa cells mediated specifically by connexin43 channels is required for continued follicular growth. Measurements of oocyte diameters revealed that oocyte growth in mutant follicles is retarded, but not arrested, despite the arrest of folliculogenesis. The mutant follicles are morphologically abnormal: the zona pellucida is poorly developed, the cytoplasm of both granulosa cells and oocytes is vacuolated, and cortical granules are absent from the oocytes. Correspondingly, the mutant oocytes obtained from 3-week grafts failed to undergo meiotic maturation and could not be fertilized, although half of the wild-type oocytes from 3-week grafted ovaries could be fertilized. We conclude that connexin43-containing gap junction channels are required for expansion of the granulosa cell population during the early stages of follicular development and that failure of the granulosa cell layers to develop properly has severe consequences for the oocyte.
哺乳动物的卵巢卵泡是一个功能性合体细胞,卵母细胞通过缝隙连接与周围的卵丘颗粒细胞相连,而卵丘细胞之间以及与壁颗粒细胞之间也通过缝隙连接相互连接。成熟卵泡中连接颗粒细胞的缝隙连接包含几种不同的连接蛋白(缝隙连接通道蛋白),包括连接蛋白32、43和45。出生后刚开始卵泡发生时就能检测到连接蛋白43的免疫反应性,并且一直持续到排卵。为了评估连接蛋白43缝隙连接对出生后卵泡发生的重要性,我们将妊娠晚期缺乏连接蛋白43(Gja1(-)/Gja1(-))的小鼠胎儿或新生幼崽的卵巢移植到成年雌性小鼠的肾囊中,让它们发育长达3周(由于突变导致的新生儿致死性,这是必要的)。移植期结束时,移植的正常(野生型或杂合子)卵巢中已发育出三级(窦状)卵泡。然而,Gja1(-)/Gja1(-)卵巢中的大多数卵泡未能形成多层结构,其影响的严重程度取决于品系背景。染料转移实验表明,在缺乏连接蛋白43的情况下,颗粒细胞之间的细胞间偶联减少但并未消除,这与存在其他连接蛋白一致。这些结果表明,由连接蛋白43通道特异性介导的颗粒细胞之间的偶联是卵泡持续生长所必需的。卵母细胞直径的测量结果显示,尽管卵泡发生停滞,但突变卵泡中的卵母细胞生长受到抑制但并未停止。突变卵泡在形态上异常:透明带发育不良,颗粒细胞和卵母细胞的细胞质均出现空泡化,并且卵母细胞中没有皮质颗粒。相应地,从3周移植卵巢中获得的突变卵母细胞未能进行减数分裂成熟,也无法受精,而来自3周移植卵巢的野生型卵母细胞中有一半能够受精。我们得出结论,在卵泡发育早期,含连接蛋白43的缝隙连接通道是颗粒细胞群体扩张所必需的,并且颗粒细胞层发育异常对卵母细胞有严重影响。