Lactational competence and involution of the mouse mammary gland require plasminogen

Author:

Lund L.R.1,Bjorn S.F.1,Sternlicht M.D.1,Nielsen B.S.1,Solberg H.1,Usher P.A.1,Osterby R.1,Christensen I.J.1,Stephens R.W.1,Bugge T.H.1,Dano K.1,Werb Z.1

Affiliation:

1. Finsen Laboratory, Copenhagen University Hospital, Strandboulevarden 49, DK-2100 Copenhagen, Denmark. lund@inet.uni2.dk

Abstract

Urokinase-type plasminogen activator expression is induced in the mouse mammary gland during development and post-lactational involution. We now show that primiparous plasminogen-deficient (Plg(−/−)) mice have seriously compromised mammary gland development and involution. All mammary glands were underdeveloped and one-quarter of the mice failed to lactate. Although the glands from lactating Plg(−/−) mice were initially smaller, they failed to involute after weaning, and in most cases they failed to support a second litter. Alveolar regression was markedly reduced and a fibrotic stroma accumulated in Plg(−/−) mice. Nevertheless, urokinase and matrix metalloproteinases (MMPs) were upregulated normally in involuting glands of Plg(−/−) mice, and fibrin did not accumulate in the glands. Heterozygous Plg(+/−) mice exhibited haploinsufficiency, with a definite, but less severe mammary phenotype. These data demonstrate a critical, dose-dependent requirement for Plg in lactational differentiation and mammary gland remodeling during involution.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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