We have used gene targeting to generate relaxin (rlx)-deficient mice. The m
ajority (15 of 17) of homozygous (rlx(-/-)) mice are fertile and produce no
rmal litters. However their mammary development is deficient; pups are unab
le to suckle and die within 24 h of birth unless cross-fostered to a wild-t
ype (rlx(+/+)) foster mother. The nipples of rlx(-/-) animals do not enlarg
e significantly during pregnancy, and their histology retains the appearanc
e of the virgin state. Breast parenchyma is somewhat underdeveloped at term
even though milk is produced. Mammary ducts become grossly dilated in thes
e animals. Heterozygous (rlx(+/-)) mice lactate normally.
The interpubic ligament does not relax during pregnancy in rlx(-/-) mice. P
lasma osmolality during late gestation was significantly higher (P < 0.001)
in rlx(-/-) mice than in wild-type controls.