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PMID: 1512297 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Coordinated expression of extracellular matrix-degrading proteinases and their inhibitors regulates mammary epithelial function during involution.

The Journal of cell biology ·Vol. 118 ·No. 5 ·1992-09-00 ·Pages 1271-82

Talhouk RS, Bissell MJ, Werb Z

Abstract

Extracellular matrix (ECM) plays an important role in the maintenance of mammary epithelial differentiation in culture. We asked whether changes in mouse mammary specific function in vivo correlate with changes in the ECM. We showed, using expression of beta-casein as a marker, that the temporal expression of ECM-degrading proteinases and their inhibitors during lactation and involution are inversely related to functional differentiation. After a lactation period of 9 d, mammary epithelial cells maintained beta-casein expression up to 5 d of involution. Two metalloproteinases, 72-kD gelatinase (and its 62-kD active form), and stromelysin, and a serine proteinase tissue plasminogen activator were detected by day four of involution, and maintained expression until at least day 10. The expression of their inhibitors, the tissue inhibitor of metalloproteinases (TIMP) and plasminogen activator inhibitor-1, preceded the onset of ECM-degrading proteinase expression and was detected by day two of involution, and showed a sharp peak of expression centered on days 4-6 of involution. When involution was accelerated by decreasing lactation to 2 d, there was an accelerated loss of beta-casein expression evident by day four and a shift in expression of ECM-remodeling proteinases and inhibitors to a focus at 2-4 d of involution. To further extend the correlation between mammary-specific function and ECM remodeling we initiated involution by sealing just one gland in an otherwise hormonally sufficient lactating animal. Alveoli in the sealed gland contained casein for at least 7 d after sealing, and closely resembled those in a lactating gland. The relative expression of TIMP in the sealed gland increased, whereas the expression of stromelysin was much lower than that of a hormone-depleted involuting gland, indicating that the higher the ratio of TIMP to ECM-degrading proteinases the slower the process of involution. To test directly the functional role of ECM-degrading proteinases in the loss of tissue-specific function we artificially perturbed the ECM-degrading proteinase-inhibitor ratio in a normally involuting gland by maintaining high concentrations of TIMP protein with the use of surgically implanted slow-release pellets. In a concentration-dependent fashion, involuting mammary glands that received TIMP implants maintained high levels of casein and delayed alveolar regression. These data suggest that the balance of ECM-degrading proteinases and their inhibitors regulates the organization of the basement membrane and the tissue-specific function of the mammary gland.(ABSTRACT TRUNCATED AT 400 WORDS)

MeSH Terms
Animals Caseins/biosynthesis,genetics Endopeptidases/metabolism Extracellular Matrix/metabolism Female Glycoproteins/metabolism Lactation Mammary Glands, Animal/enzymology,physiology Matrix Metalloproteinase 3 Metalloendopeptidases/antagonists & inhibitors,metabolism Mice Protease Inhibitors/metabolism Tissue Inhibitor of Metalloproteinases
Chemicals
Caseins Glycoproteins Protease Inhibitors Tissue Inhibitor of Metalloproteinases Endopeptidases Metalloendopeptidases Matrix Metalloproteinase 3
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Talhouk R S
Division of Cell and Molecular Biology, Lawrence Berkeley Laboratory, CA 94720.
Bissell M J
Werb Z
References (41)
41 references, click to expand
  1. Regulation of rat mammary gene expression by extracellular matrix components.
    Exp Cell Res. 1987 Dec;173(2):322-40 PMID: 3691666
  2. Effects of inhibition of basement membrane collagen deposition on rat mammary gland development.
    Dev Biol. 1980 Dec;80(2):253-6 PMID: 7450284
  3. Metalloproteinases mediate extracellular matrix degradation by cells from mouse blastocyst outgrowths.
    Development. 1992 Feb;114(2):447-56 PMID: 1317291
  4. A novel metalloproteinase gene specifically expressed in stromal cells of breast carcinomas.
    Nature. 1990 Dec 20-27;348(6303):699-704 PMID: 1701851
  5. Calcium-dependent and calcium-independent gelatinolytic proteinase activities of the rat ventral prostate and its secretion: characterization and effect of castration and testosterone treatment.
    Biol Reprod. 1991 May;44(5):776-85 PMID: 1868137
  6. Designer microenvironments for the analysis of cell and tissue function.
    Curr Opin Cell Biol. 1990 Oct;2(5):864-74 PMID: 2083086
  7. Metalloproteinases and their inhibitors in matrix remodeling.
    Trends Genet. 1990 Apr;6(4):121-5 PMID: 2132731
  8. Expression of extracellular matrix components is regulated by substratum.
    J Cell Biol. 1990 Apr;110(4):1405-15 PMID: 2182652
  9. Inhibition of mouse mammary ductal morphogenesis and down-regulation of the EGF receptor by epidermal growth factor.
    Dev Biol. 1990 Feb;137(2):425-33 PMID: 2303169
  10. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction.
    Anal Biochem. 1987 Apr;162(1):156-9 PMID: 2440339
  11. Posttranscriptional regulation of cellular gene expression by the c-myc oncogene.
    Mol Cell Biol. 1989 Jan;9(1):124-34 PMID: 2467185
  12. Genes for extracellular-matrix-degrading metalloproteinases and their inhibitor, TIMP, are expressed during early mammalian development.
    Genes Dev. 1989 Jun;3(6):848-59 PMID: 2744464
  13. Molecular cloning of complementary DNA to mouse tissue plasminogen activator mRNA and its expression during F9 teratocarcinoma cell differentiation.
    J Biol Chem. 1988 Jan 25;263(3):1563-9 PMID: 2826484
  14. Characterization and expression of a murine gene homologous to human EPA/TIMP: a virus-induced gene in the mouse.
    EMBO J. 1987 Mar;6(3):651-7 PMID: 3034603
  15. Expression pattern of a gene for a secreted metalloproteinase during late stages of tumor progression.
    Mol Carcinog. 1988;1(1):13-9 PMID: 3151258
  16. Mammary function during the nonlactating period: enzyme, lactose, protein concentrations, and pH of mammary secretions.
    J Dairy Sci. 1987 Jan;70(1):20-8 PMID: 3571623
  17. Ultrastructural changes accompanying involution of the mammary gland in the albino rat.
    J Endocrinol. 1971 Sep;51(1):127-35 PMID: 5166462
  18. "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.
    Anal Biochem. 1984 Feb;137(1):266-7 PMID: 6329026
  19. Electron microscopy of milk secretion in the mammary gland of the C3H/Crgl mouse. III. Cytomorphology of the involuting gland.
    J Natl Cancer Inst. 1963 Feb;30:241-67 PMID: 13999854
  20. Ovarian plasminogen activator: relationship to ovulation and hormonal regulation.
    Cell. 1975 Nov;6(3):387-94 PMID: 212205
  21. Apoptotic cell death and tissue remodelling during mouse mammary gland involution.
    Development. 1992 May;115(1):49-58 PMID: 1638991
  22. Extracellular matrix metalloproteinases in tumor invasion and metastasis.
    Cancer Treat Res. 1991;53:421-40 PMID: 1672089
  23. Proteinases of the mammary gland: developmental regulation in vivo and vectorial secretion in culture.
    Development. 1991 Jun;112(2):439-49 PMID: 1794314
  24. Control of mammary epithelial differentiation: basement membrane induces tissue-specific gene expression in the absence of cell-cell interaction and morphological polarity.
    J Cell Biol. 1991 Dec;115(5):1383-95 PMID: 1955479
  25. Cell culture models of differentiation.
    FASEB J. 1991 Mar 1;5(3):287-94 PMID: 2001788
  26. Immunohistochemical distribution of type IV collagenase in normal, benign, and malignant breast tissue.
    Am J Pathol. 1990 Mar;136(3):585-92 PMID: 2156430
  27. In vivo analyses of integrin beta 1 subunit function in fibronectin matrix assembly.
    J Cell Biol. 1990 May;110(5):1813-23 PMID: 2186050
  28. Extracellular matrix and hormones transcriptionally regulate bovine beta-casein 5' sequences in stably transfected mouse mammary cells.
    Proc Natl Acad Sci U S A. 1990 Dec;87(23):9118-22 PMID: 2251252
  29. Epithelium-dependent extracellular matrix synthesis in transforming growth factor-beta 1-growth-inhibited mouse mammary gland.
    J Cell Biol. 1990 Jun;110(6):2209-19 PMID: 2351697
  30. Enhanced synthesis and secretion of type IV collagen and entactin during adipose conversion of 3T3-L1 cells and production of unorthodox laminin complex.
    J Biol Chem. 1988 Nov 5;263(31):16163-9 PMID: 2460444
  31. A novel regulatory mechanism for whey acidic protein gene expression.
    Cell Regul. 1989 Nov;1(1):45-54 PMID: 2519617
  32. Mammary gland function during involution.
    J Dairy Sci. 1989 Jun;72(6):1637-46 PMID: 2668360
  33. Functional differentiation and alveolar morphogenesis of primary mammary cultures on reconstituted basement membrane.
    Development. 1989 Feb;105(2):223-35 PMID: 2806122
  34. Structure-function relationships in the collagenase family member transin.
    J Biol Chem. 1988 Aug 25;263(24):11892-9 PMID: 2841336
  35. The role of interstitial collagens in cleft formation of mouse embryonic submandibular gland during initial branching.
    Development. 1988 Jun;103(2):259-67 PMID: 2852095
  36. Cell-associated plasminogen activation: regulation and physiological functions.
    Annu Rev Cell Biol. 1988;4:93-126 PMID: 3143380
  37. Influence of a reconstituted basement membrane and its components on casein gene expression and secretion in mouse mammary epithelial cells.
    Proc Natl Acad Sci U S A. 1987 Jan;84(1):136-40 PMID: 3467345
  38. Investigation of mouse mammary ductal growth regulation using slow-release plastic implants.
    J Dairy Sci. 1987 Sep;70(9):1981-90 PMID: 3668054
  39. 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):667-76 PMID: 6179984
  40. Elvax 40P implants: sustained, local release of bioactive molecules influencing mammary ductal development.
    Dev Biol. 1982 Sep;93(1):272-8 PMID: 7128936
  41. Removal of basement membrane in the involuting breast.
    Lab Invest. 1976 May;34(5):455-62 PMID: 5627
Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1992-09-00
Pages
1271-82
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2289583
Subset
IM
Grants
NICHD NIH HHS · HD 23539 · United States
NIEHS NIH HHS · T32ES07106 · United States
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