Hirobe S, He W W, Lee M M, Donahoe P K
Pediatric Surgical Research Laboratory, Massachusetts General Hospital, Boston 02114.
Endocrinology. 1992 Aug;131(2):854-62. doi: 10.1210/endo.131.2.1639028.
In males, Mullerian inhibiting substance (MIS) mRNA was first detected on the medial aspect of the urogenital ridge early on the morning of day 13 of gestation before testicular differentiation was evident, and localized to the more obvious Sertoli cells later on embryonic day 13. MIS transcripts remained at maximal levels between 14.5 and 17.5 days gestation, while the Mullerian duct involutes, and remained high until birth. MIS gene expression decreased progressively after birth and, as germ cell meiosis increased, became barely detectable in the Sertoli cells of the seminiferous tubules. In female rats, MIS mRNA was first detected in the single layer of cuboidal granulosa cells surrounding larger primary follicles 3 days after birth, coincident with the initiation of follicular growth. As follicular growth progressed, MIS mRNA expression was high in preantral and small antral follicles, especially in those granulosa cells closest to the oocyte. MIS mRNA expression decreased gradually in larger antral follicles, remaining prominent only in the cumulus cells and the dividing population of granulosa cells closest to the lumen. MIS gene expression was absent in follicles with features of atresia and in the larger antral follicles. The expression of MIS mRNA in actively dividing Sertoli and granulosa cells correlates with the stages of germ cell division. These findings are suggestive of a role for MIS in the control of germ cell maturation.
在雄性中,妊娠第13天清晨,在睾丸分化明显之前,首先在泌尿生殖嵴内侧检测到苗勒管抑制物质(MIS)mRNA,随后在胚胎第13天定位到更明显的支持细胞。在妊娠14.5至17.5天之间,苗勒管退化时,MIS转录本保持在最高水平,并一直维持到出生时仍保持高水平。出生后,MIS基因表达逐渐下降,随着生殖细胞减数分裂增加,在曲细精管的支持细胞中几乎检测不到。在雌性大鼠中,出生后3天,在围绕较大初级卵泡的单层立方形颗粒细胞中首次检测到MIS mRNA,这与卵泡生长的开始同时发生。随着卵泡生长的进行,MIS mRNA在窦前卵泡和小窦状卵泡中表达较高,尤其是在最靠近卵母细胞的颗粒细胞中。在较大的窦状卵泡中,MIS mRNA表达逐渐降低,仅在卵丘细胞和最靠近管腔的颗粒细胞分裂群体中仍很突出。闭锁卵泡和较大的窦状卵泡中不存在MIS基因表达。活跃分裂的支持细胞和颗粒细胞中MIS mRNA的表达与生殖细胞分裂阶段相关。这些发现提示MIS在控制生殖细胞成熟中起作用。