Reduced expression of the PTH/PTHrP receptor during development of the mammary gland influences the function of the nipple during lactation

Dev Dyn. 2005 Jul;233(3):794-803. doi: 10.1002/dvdy.20406.

Abstract

Signaling by the parathyroid hormone/parathyroid hormone-related protein receptor (Ppr) is necessary for mammary gland development beyond the early induction stage in mice. We used a series of murine models of reduced Ppr expression to determine how diminished receptor signaling influences mammary development. Reduction of Ppr expression to very low levels prevented mammary gland development. A less-severe reduction in Ppr expression permitted progression of mammary gland development beyond the induction stage, but the nipples of these mice were dramatically smaller than those of controls, with altered epidermis and connective tissue. Mothers with reduced expression of Ppr could not successfully nurse pups; however, the lactating glands did produce milk but could not efficiently deliver it. This finding was associated with reduced levels of matrix metalloproteinase-2 and an absence of pregnancy-associated remodeling of connective tissue matrix in the nipple. Reduced smooth muscle appears to underlie the majority of nipple deficiencies in mice with lower levels of the Ppr expression.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Female
  • Gene Expression Regulation, Developmental / genetics*
  • Lactation / physiology*
  • Mammary Glands, Animal / growth & development*
  • Mammary Glands, Animal / metabolism*
  • Matrix Metalloproteinase 2 / metabolism
  • Mice
  • Mice, Transgenic
  • Models, Genetic
  • Nipples / growth & development
  • Nipples / physiology*
  • Parathyroid Hormone-Related Protein / metabolism*
  • Phenotype
  • Pregnancy
  • Receptors, Parathyroid Hormone / metabolism*

Substances

  • Parathyroid Hormone-Related Protein
  • Receptors, Parathyroid Hormone
  • Matrix Metalloproteinase 2