Maternal Hoxa10 is required for pinopod formation in the development of mouse uterine receptivity to embryo implantation

Citation
Cn. Bagot et al., Maternal Hoxa10 is required for pinopod formation in the development of mouse uterine receptivity to embryo implantation, DEV DYNAM, 222(3), 2001, pp. 538-544
Citations number
23
Categorie Soggetti
Cell & Developmental Biology
Journal title
DEVELOPMENTAL DYNAMICS
ISSN journal
10588388 → ACNP
Volume
222
Issue
3
Year of publication
2001
Pages
538 - 544
Database
ISI
SICI code
1058-8388(200111)222:3<538:MHIRFP>2.0.ZU;2-H
Abstract
Hoxa10 is a homeobox gene that is expressed both during the embryogenesis o f the genitourinary tract and in the adult reproductive tract. Maternal Hox a10 expression is necessary for endometrial receptivity to blastocyst impla ntation. The mechanism by which Hoxa10 induces endometrial development to a state of receptivity is unknown as Hoxa10-deficient endometrium appears hi stologically normal. We altered the expression of Hoxa10 in the uterus of c ycling adult female mice and examined the uterus at the time of implantatio n by transmission electron microscopy for alterations in epithelial morphol ogy. Pinopods are projections on the surface of the uterine endometrial epi thelial cells that develop transiently at the time of endometrial receptivi ty. Blocking Hoxa10 expression by transfection of Hoxa10 antisense into the cycling mouse uterus before implantation dramatically decreased pinopod nu mber. Constitutively expressing Hoxa10 in the uterus just before the normal time of pinopod formation resulted in increased pinopod number. Therefore, Hoxa10 is necessary for pinopod development. Hox genes have been implicate d in both the regulation of cellular proliferation and the determination of developmental fate. Hoxa10 exemplifies this dual role in the uterus by reg ulating both endometrial stromal cell proliferation and epithelial cell mor phogenesis. Taken together, these results demonstrate that maternal Hoxa10 has an essential role in pinopod development and this function of Hoxa10 li kely contributes to endometrial receptivity for the purpose of blastocyst i mplantation. (C) 2001 Wiley-Liss, Inc.