Racowsky C, Satterlie R A
Dev Biol. 1985 Mar;108(1):191-202. doi: 10.1016/0012-1606(85)90022-3.
Heterologous intercellular communication was determined qualitatively by lucifer yellow dye transfer and quantitatively by transfer of radiolabeled uridine metabolites and electrical current in hamster oocyte-cumulus complexes during meiotic maturation in vitro and in vivo. In addition, changes in cell resting potentials during maturation were recorded. Significantly less time was required for germinal vesicle breakdown (GVBD) in oocytes matured in vitro than in oocytes stimulated in vivo (1.81 +/- 0.06 hr, N = 13 vs 2.46 +/- 0.07 hr, N = 18, respectively, P less than 0.001). Resting potentials of the oocyte (RP-o) and cumulus cells (RP-c) significantly increased contemporaneously with GVBD in vitro (RP-o: from -18.9 +/- 3.2 mV to -33.2 +/- 2.9 mV, P less than 0.001; RP-c: from -16.3 +/- 1.9 mV to -27.5 +/- 2.6 mV, P less than 0.001) and in vivo after hCG injection (RP-o: from -16.8 +/- 5.9 mV to -30.1 +/- 3.9 mV, P less than 0.001; RP-c: from -15.5 +/- 3.8 mV to -26.3 +/- 3.2 mV, P less than 0.001). RP-o and RP-c progressively increased with time of culture up to 7 hr (maximum time examined) while the values reached maxima in in vivo matured oocytes 4.5 hr post-hCG and subsequently declined concomitant with the onset of cumulus expansion. Cumulus to oocyte coupling decreased progressively with time after release from meiotic arrest both in vitro and in vivo, as assessed by a progressive reduction in transfer of either uridine marker or lucifer yellow from the cumulus cell to the oocyte. By 4.5 hr after hCG injection, cumulus expansion had begun in 100% of complexes examined. Expansion was extensive by 7 hr post-hCG and spread of lucifer yellow from a cumulus cell was limited to very few adjacent cumulus cells. Oocyte to cumulus cell metabolic coupling also decreased progressively with time in both treatment groups. Examination of the extent of heterologous ionic coupling revealed that ionic coupling exhibited biphasic and, bidirectionally parallel, increases during meiotic maturation. While these temporal changes were observed in both groups, the coupling ratios were much greater in those complexes matured in vitro than in vivo. These results show that dye, metabolic, and electrical coupling exist between the immature hamster oocyte and its surrounding cumulus cells but that during the early stages of meiosis, metabolic and dye coupling decrease, while electrical coupling increases biphasically.
通过荧光素黄染料转移定性测定异源细胞间通讯,并通过体外和体内减数分裂成熟过程中仓鼠卵母细胞-卵丘复合体中放射性标记的尿苷代谢物转移和电流定量测定。此外,记录了成熟过程中细胞静息电位的变化。体外成熟的卵母细胞发生生发泡破裂(GVBD)所需的时间明显少于体内刺激的卵母细胞(分别为1.81±0.06小时,N = 13,对比2.46±0.07小时,N = 18,P<0.001)。在体外,卵母细胞(RP-o)和卵丘细胞(RP-c)的静息电位在GVBD同时显著增加(RP-o:从-18.9±3.2 mV增加到-33.2±2.9 mV,P<0.001;RP-c:从-16.3±1.9 mV增加到-27.5±2.6 mV,P<0.001),在体内注射hCG后也是如此(RP-o:从-16.8±5.9 mV增加到-30.1±3.9 mV,P<0.001;RP-c:从-15.5±3.8 mV增加到-26.3±3.2 mV,P<0.001)。RP-o和RP-c随着培养时间的延长逐渐增加,直至7小时(检查的最长时间),而在体内成熟的卵母细胞中,hCG注射后4.5小时达到最大值,随后随着卵丘扩展的开始而下降。从减数分裂阻滞释放后,无论是体外还是体内,卵丘与卵母细胞的耦合随着时间的推移逐渐降低,这通过从卵丘细胞向卵母细胞转移尿苷标记物或荧光素黄的逐渐减少来评估。hCG注射后4.5小时,100%检查的复合体开始出现卵丘扩展。hCG注射后7小时扩展广泛,荧光素黄从一个卵丘细胞扩散仅限于极少数相邻的卵丘细胞。在两个治疗组中,卵母细胞向卵丘细胞的代谢耦合也随着时间的推移逐渐降低。对异源离子耦合程度的检查表明,离子耦合在减数分裂成熟过程中呈现双相且双向平行增加。虽然在两组中都观察到了这些时间变化,但体外成熟的复合体中的耦合比率比体内成熟的要大得多。这些结果表明,未成熟的仓鼠卵母细胞与其周围卵丘细胞之间存在染料、代谢和电耦合,但在减数分裂的早期阶段,代谢和染料耦合减少,而电耦合双相增加。