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. 1997 Apr;190(Pt 3):405–416. doi: 10.1046/j.1469-7580.1997.19030405.x

Involution of the sheep mammary gland

L TATARCZUCH 1, C PHILIP 1, C S LEE 1
PMCID: PMC1467620  PMID: 9147226

Abstract

Changes in the ovine mammary gland epithelium during initiated involution were studied by light and electron microscopy. Apoptosis of the duct and alveolar epithelial cells was first identified at 2 d after weaning, reached a peak at 4 d and then progressed gradually thereafter. Apoptotic cells were phagocytosed by intraepithelial macrophages and alveolar epithelial cells. Occasional apoptotic epithelial cells were observed in the alveolar and duct lumina. The highly vacuolated cells in the alveolar and duct lumina were confirmed to be macrophages as they were CD45+, MHC class II+. Changes in myoepithelial cells involved shrinkage and extension of cytoplasmic processes into the underlying stroma and no apoptosis was observed. Regression of the blood capillaries was also by apoptosis. The resulting apoptotic bodies were either taken up by adjacent endothelial cells or were shed into the capillary lumen to be phagocytosed later by mural endothelial cells or blood monocytes. The mammary glands were completely involuted by 30 d after weaning. It was concluded that the mammary gland involutes by apoptosis, a process which allows deletion of cells without the loss of the basic architecture and the integrity of the epithelial lining of the gland.

Keywords: Ewe, mammary gland regression, apoptosis

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Selected References

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  1. Andersson L. M., Dundas S. R., O'Hare M. J., Gusterson B. A., Warburton M. J. Synthesis of gelatinases by rat mammary epithelial and myoepithelial cell lines. Exp Cell Res. 1994 Jun;212(2):389–392. doi: 10.1006/excr.1994.1159. [DOI] [PubMed] [Google Scholar]
  2. Dickson S. R., Warburton M. J. Enhanced synthesis of gelatinase and stromelysin by myoepithelial cells during involution of the rat mammary gland. J Histochem Cytochem. 1992 May;40(5):697–703. doi: 10.1177/40.5.1315355. [DOI] [PubMed] [Google Scholar]
  3. Guenette R. S., Corbeil H. B., Léger J., Wong K., Mézl V., Mooibroek M., Tenniswood M. Induction of gene expression during involution of the lactating mammary gland of the rat. J Mol Endocrinol. 1994 Feb;12(1):47–60. doi: 10.1677/jme.0.0120047. [DOI] [PubMed] [Google Scholar]
  4. Helminen H. J., Ericsson J. L. Studies on mammary gland involution. II. Ultrastructural evidence for auto- and heterophagocytosis. J Ultrastruct Res. 1968 Nov;25(3):214–227. doi: 10.1016/s0022-5320(68)80070-x. [DOI] [PubMed] [Google Scholar]
  5. Holst B. D., Hurley W. L., Nelson D. R. Involution of the bovine mammary gland: histological and ultrastructural changes. J Dairy Sci. 1987 May;70(5):935–944. doi: 10.3168/jds.S0022-0302(87)80097-8. [DOI] [PubMed] [Google Scholar]
  6. Lee C. S., Gogolin-Ewens K., White T. R., Brandon M. R. Studies on the distribution of binucleate cells in the placenta of the sheep with a monoclonal antibody SBU-3. J Anat. 1985 Jun;140(Pt 4):565–576. [PMC free article] [PubMed] [Google Scholar]
  7. Lee C. S., Outteridge P. M. Leucocytes of sheep colostrum, milk and involution secretion, with particular reference to ultrastructure and lymphocyte sub-populations. J Dairy Res. 1981 Jun;48(2):225–237. doi: 10.1017/s0022029900021646. [DOI] [PubMed] [Google Scholar]
  8. Mackay C. R., Maddox J. F., Brandon M. R. A monoclonal antibody to the p220 component of sheep LCA identifies B cells and a unique lymphocyte subset. Cell Immunol. 1987 Nov;110(1):46–55. doi: 10.1016/0008-8749(87)90100-6. [DOI] [PubMed] [Google Scholar]
  9. Mackay C. R., Maddox J. F., Gogolin-Ewens K. J., Brandon M. R. Characterization of two sheep lymphocyte differentiation antigens, SBU-T1 and SBU-T6. Immunology. 1985 Aug;55(4):729–737. [PMC free article] [PubMed] [Google Scholar]
  10. Maddox J. F., Mackay C. R., Brandon M. R. Surface antigens, SBU-T4 and SBU-T8, of sheep T lymphocyte subsets defined by monoclonal antibodies. Immunology. 1985 Aug;55(4):739–748. [PMC free article] [PubMed] [Google Scholar]
  11. Maddox J. F., Mackay C. R., Brandon M. R. The sheep analogue of leucocyte common antigen (LCA). Immunology. 1985 Jun;55(2):347–353. [PMC free article] [PubMed] [Google Scholar]
  12. Martinez-Hernandez A., Fink L. M., Pierce G. B. Removal of basement membrane in the involuting breast. Lab Invest. 1976 May;34(5):455–462. [PubMed] [Google Scholar]
  13. Nickerson S. C. Immunological aspects of mammary involution. J Dairy Sci. 1989 Jun;72(6):1665–1678. doi: 10.3168/jds.S0022-0302(89)79278-X. [DOI] [PubMed] [Google Scholar]
  14. O'Shea J. D., Nightingale M. G., Chamley W. A. Changes in small blood vessels during cyclical luteal regression in sheep. Biol Reprod. 1977 Sep;17(2):162–177. doi: 10.1095/biolreprod17.2.162. [DOI] [PubMed] [Google Scholar]
  15. Oliver S. P., Sordillo L. M. Approaches to the manipulation of mammary involution. J Dairy Sci. 1989 Jun;72(6):1647–1664. doi: 10.3168/jds.S0022-0302(89)79277-8. [DOI] [PubMed] [Google Scholar]
  16. Puri N. K., Gorrell M. D., Brandon M. R. Sheep MHC class II molecules. I. Immunochemical characterization. Immunology. 1987 Dec;62(4):567–573. [PMC free article] [PubMed] [Google Scholar]
  17. Radnor C. J. Myoepithelium in involuting mammary glands of the rat. J Anat. 1972 Sep;112(Pt 3):355–365. [PMC free article] [PubMed] [Google Scholar]
  18. Sordillo L. M., Nickerson S. C. Morphologic changes in the bovine mammary gland during involution and lactogenesis. Am J Vet Res. 1988 Jul;49(7):1112–1120. [PubMed] [Google Scholar]
  19. Sordillo L. M., Oliver S. P., Nickerson S. C. Caprine mammary differentiation and initiation of lactation following prepartum colchicine infusion. Int J Biochem. 1984;16(12):1265–1272. doi: 10.1016/0020-711x(84)90226-x. [DOI] [PubMed] [Google Scholar]
  20. Strange R., Li F., Saurer S., Burkhardt A., Friis R. R. Apoptotic cell death and tissue remodelling during mouse mammary gland involution. Development. 1992 May;115(1):49–58. doi: 10.1242/dev.115.1.49. [DOI] [PubMed] [Google Scholar]
  21. Talhouk R. S., Bissell M. J., Werb Z. Coordinated expression of extracellular matrix-degrading proteinases and their inhibitors regulates mammary epithelial function during involution. J Cell Biol. 1992 Sep;118(5):1271–1282. doi: 10.1083/jcb.118.5.1271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Walker N. I., Bennett R. E., Kerr J. F. Cell death by apoptosis during involution of the lactating breast in mice and rats. Am J Anat. 1989 May;185(1):19–32. doi: 10.1002/aja.1001850104. [DOI] [PubMed] [Google Scholar]
  23. Warburton M. J., Mitchell D., Ormerod E. J., Rudland P. Distribution of myoepithelial cells and basement membrane proteins in the resting, pregnant, lactating, and involuting rat mammary gland. J Histochem Cytochem. 1982 Jul;30(7):667–676. doi: 10.1177/30.7.6179984. [DOI] [PubMed] [Google Scholar]

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