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Female infertility in mice deficient in midkine and pleiotrophin, which form a distinct family of growth factors
Author(s) -
Muramatsu Hisako,
Zou Peng,
Kurosawa Nobuyuki,
IchiharaTanaka Keiko,
Maruyama Kiyoko,
Inoh Kazuhiko,
Sakai Takayuki,
Chen Lan,
Sato Masahiro,
Muramatsu Takashi
Publication year - 2006
Publication title -
genes to cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 115
eISSN - 1365-2443
pISSN - 1356-9597
DOI - 10.1111/j.1365-2443.2006.01028.x
Subject(s) - pleiotrophin , midkine , biology , estrous cycle , endocrinology , medicine , ovulation , ovary , follicular phase , uterus , receptor , growth factor , andrology , genetics , hormone
Midkine and pleiotrophin form a family of growth factors. Mice deficient in one of the genes show few abnormalities on reproduction and development. To understand their roles in these processes, we produced mice deficient in both genes; the double deficient mice were born in only one third the number expected by Mendelian segregation and 4 weeks after birth weighed about half as much as wild‐type mice. Most of the female double deficient mice were infertile. In these mice, the numbers of mature follicles and of ova at ovulation were reduced compared to numbers in wild‐type mice. Both midkine and pleiotrophin were expressed in the follicular epithelium and granulosa cells of the ovary. The expression of these factors in the uterus was dramatically altered during the estrous cycle. The diestrus and proestrus periods were long and the estrus period was short in the double deficient mice, indicating the role of the factors in the estrous cycle. Furthermore, vaginal abnormality was found in about half of the double deficient mice. These abnormalities in combination resulted in female infertility. Therefore, midkine and pleiotrophin, together with their signaling receptors, play important roles in the female reproductive system.