|
|
|
|||
| Home Help Feedback Subscriptions Archive Search Table of Contents | ||||
Development, Vol 112, Issue 2 439-449, Copyright © 1991 by Company of Biologists
JOURNAL ARTICLES |
RS Talhouk, JR Chin, EN Unemori, Z Werb and MJ Bissell
Division of Cell and Molecular Biology, Lawrence Berkeley Laboratory, Berkely, CA 94720.
The extracellular matrix (ECM) is an important regulator of mammary epithelial cell function both in vivo and in culture. Substantial remodeling of ECM accompanies the structural changes in the mammary gland during gestation, lactation and involution. However, little is known about the nature of the enzymes and the processes involved. We have characterized and studied the regulation of cell-associated and secreted mammary gland proteinases active at neutral pH that may be involved in degradation of the ECM during the different stages of mammary development. Mammary tissue extracts from virgin and pregnant CD-1 mice resolved by zymography contained three major proteinases of 60K (K = 10(3) Mr), 68K and 70K that degraded denatured collagen. These three gelatinases were completely inhibited by the tissue inhibitor of metalloproteinases. Proteolytic activity was lowest during lactation especially for the 60K gelatinase which was shown to be the activated form of the 68K gelatinase. The activated 60K form decreased prior to parturition but increased markedly after the first two days of involution. An additional gelatin-degrading proteinase of 130K was expressed during the first three days of involution and differed from the other gelatinases by its lack of inhibition by the tissue inhibitor of metalloproteinases. The activity of the casein-degrading proteinases was lowest during lactation. Three caseinolytic activities were detected in mammary tissue extracts. A novel 26K cell-associated caseinase--a serine arginine-esterase--was modulated at different stages of mammary development. The other caseinases, at 92K and a larger than 100K, were not developmentally regulated. To find out which cell type produced the proteinases in the mammary gland, we isolated and cultured mouse mammary epithelial cells. Cells cultured on different substrata produced the full spectrum of gelatinases and caseinases seen in the whole gland thus implicating the epithelial cells as a major source of these enzymes. Analysis of proteinases secreted by cells grown on a reconstituted basement membrane showed that gelatinases were secreted preferentially in the direction of the basement membrane. The temporal pattern of expression of these proteinases and the basal secretion of gelatinases by epithelial cells suggest their involvement in the remodelling of the extracellular matrix during the different stages of mammary development and thus modulation of mammary cell function.
This article has been cited by other articles:
![]() |
M. Simian, A. Molinolo, and C. Lanari Involvement of Matrix Metalloproteinase Activity in Hormone-Induced Mammary Tumor Regression Am. J. Pathol., January 1, 2006; 168(1): 270 - 279. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Sumida, Y. Itahana, H. Hamakawa, and P.-Y. Desprez Reduction of Human Metastatic Breast Cancer Cell Aggressiveness on Introduction of Either Form A or B of the Progesterone Receptor and Then Treatment with Progestins Cancer Res., November 1, 2004; 64(21): 7886 - 7892. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. S. Samuel, E. N. Unemori, I. Mookerjee, R. A. D. Bathgate, S. L. Layfield, J. Mak, G. W. Tregear, and X.-J. Du Relaxin Modulates Cardiac Fibroblast Proliferation, Differentiation, and Collagen Production and Reverses Cardiac Fibrosis in Vivo Endocrinology, September 1, 2004; 145(9): 4125 - 4133. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. P. Bailey, K. M. Nieport, M. P. Herbst, S. Srivastava, R. A. Serra, and N. D. Horseman Prolactin and Transforming Growth Factor-{beta} Signaling Exert Opposing Effects on Mammary Gland Morphogenesis, Involution, and the Akt-Forkhead Pathway Mol. Endocrinol., May 1, 2004; 18(5): 1171 - 1184. [Abstract] [Full Text] [PDF] |
||||
![]() |
B Safieh-Garabedian, G M Mouneimne, W El-Jouni, M Khattar, and R Talhouk The effect of endotoxin on functional parameters of mammary CID-9 cells Reproduction, March 1, 2004; 127(3): 397 - 406. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Sapi The Role of CSF-1 in Normal Physiology of Mammary Gland and Breast Cancer: An Update Experimental Biology and Medicine, January 1, 2004; 229(1): 1 - 11. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. Novaro, D. C. Radisky, N. E. R. Castro, A. Weisz, and M. J. Bissell Malignant Mammary Cells Acquire Independence from Extracellular Context for Regulation of Estrogen Receptor {alpha} Clin. Cancer Res., January 1, 2004; 10(1): 402S - 409S. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Daniel, N. Meyer-Morse, E. K. Bergsland, K. Dehne, L. M. Coussens, and D. Hanahan Immune Enhancement of Skin Carcinogenesis by CD4+ T Cells J. Exp. Med., April 21, 2003; 197(8): 1017 - 1028. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. E. Welm, K. W. Freeman, M. Chen, A. Contreras, D. M. Spencer, and J. M. Rosen Inducible dimerization of FGFR1: development of a mouse model to analyze progressive transformation of the mammary gland J. Cell Biol., May 13, 2002; 157(4): 703 - 714. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Rodriguez-Manzaneque, T. F. Lane, M. A. Ortega, R. O. Hynes, J. Lawler, and M. L. Iruela-Arispe Thrombospondin-1 suppresses spontaneous tumor growth and inhibits activation of matrix metalloproteinase-9 and mobilization of vascular endothelial growth factor PNAS, October 12, 2001; (2001) 171460498. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. A. Wood and M. C. Archer Matrix Metalloproteinases-2 and 9 Do Not Play a Role in the Growth of Preneoplastic Liver Lesions in F344 Rats Experimental Biology and Medicine, September 1, 2001; 226(8): 799 - 803. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Simian, Y. Hirai, M. Navre, Z. Werb, A. Lochter, and M. J. Bissell The interplay of matrix metalloproteinases, morphogens and growth factors is necessary for branching of mammary epithelial cells Development, August 15, 2001; 128(16): 3117 - 3131. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Jian, P. L. Jones, Q. Li, E. R. Mohler III, F. J. Schoen, and R. J. Levy Matrix Metalloproteinase-2 Is Associated with Tenascin-C in Calcific Aortic Stenosis Am. J. Pathol., July 1, 2001; 159(1): 321 - 327. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. L. Schwertfeger, M. M. Richert, and S. M. Anderson Mammary Gland Involution Is Delayed by Activated Akt in Transgenic Mice Mol. Endocrinol., June 1, 2001; 15(6): 867 - 881. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Di Matola, F. Mueller, G. Fenzi, G. Rossi, M. Bifulco, L. A. Marzano, and M. Vitale Serum Withdrawal-Induced Apoptosis in Thyroid Cells Is Caused by Loss of Fibronectin-Integrin Interaction J. Clin. Endocrinol. Metab., March 1, 2000; 85(3): 1188 - 1193. [Abstract] [Full Text] |
||||
![]() |
P Pujuguet, M Simian, J Liaw, R Timpl, Z Werb, and M. Bissell Nidogen-1 regulates laminin-1-dependent mammary-specific gene expression J. Cell Sci., January 3, 2000; 113(5): 849 - 858. [Abstract] [PDF] |
||||
![]() |
L. M. Coussens, W. W. Raymond, G. Bergers, M. Laig-Webster, O. Behrendtsen, Z. Werb, G. H. Caughey, and D. Hanahan Inflammatory mast cells up-regulate angiogenesis during squamous epithelial carcinogenesis Genes & Dev., June 1, 1999; 13(11): 1382 - 1397. [Abstract] [Full Text] |
||||
![]() |
G. Giannelli, A. Pozzi, W. G. Stetler-Stevenson, H. A. Gardner, and V. Quaranta Expression of Matrix Metalloprotease-2-Cleaved Laminin-5 in Breast Remodeling Stimulated by Sex Steroids Am. J. Pathol., April 1, 1999; 154(4): 1193 - 1201. [Abstract] [Full Text] [PDF] |
||||
![]() |
P.-Y. Desprez, C. Q. Lin, N. Thomasset, C. J. Sympson, M. J. Bissell, and J. Campisi A Novel Pathway for Mammary Epithelial Cell Invasion Induced by the Helix-Loop-Helix Protein Id-1 Mol. Cell. Biol., August 1, 1998; 18(8): 4577 - 4588. [Abstract] [Full Text] |
||||
![]() |
N. Thomasset, A. Lochter, C. J. Sympson, L. R. Lund, D. R. Williams, O. Behrendtsen, Z. Werb, and M. J. Bissell Expression of Autoactivated Stromelysin-1 in Mammary Glands of Transgenic Mice Leads to a Reactive Stroma During Early Development Am. J. Pathol., August 1, 1998; 153(2): 457 - 467. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. Sapi, M. B. Flick, S. Rodoy, D. Carter, and B. M. Kacinski Expression of CSF-I and CSF-I Receptor by Normal Lactating Mammary Epithelial Cells Reproductive Sciences, March 1, 1998; 5(2): 94 - 101. [Abstract] [PDF] |
||||
![]() |
P. L. Jones, J. Crack, and M. Rabinovitch Regulation of Tenascin-C, a Vascular Smooth Muscle Cell Survival Factor that Interacts with the alpha vbeta 3 Integrin to Promote Epidermal Growth Factor Receptor Phosphorylation and Growth J. Cell Biol., October 6, 1997; 139(1): 279 - 293. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Lund, J Romer, N Thomasset, H Solberg, C Pyke, M. Bissell, K Dano, and Z Werb Two distinct phases of apoptosis in mammary gland involution: proteinase-independent and -dependent pathways Development, January 1, 1996; 122(1): 181 - 193. [Abstract] [PDF] |
||||
![]() |
N Boudreau, C. Sympson, Z Werb, and M. Bissell Suppression of ICE and apoptosis in mammary epithelial cells by extracellular matrix Science, February 10, 1995; 267(5199): 891 - 893. [Abstract] [PDF] |
||||
![]() |
P. Jones, N Boudreau, C. Myers, H. Erickson, and M. Bissell Tenascin-C inhibits extracellular matrix-dependent gene expression in mammary epithelial cells. Localization of active regions using recombinant tenascin fragments J. Cell Sci., January 2, 1995; 108(2): 519 - 527. [Abstract] [PDF] |
||||
![]() |
I. Zucchi, L. Bini, R. Valaperta, A. Ginestra, D. Albani, L. Susani, J. C. Sanchez, S. Liberatori, B. Magi, R. Raggiaschi, et al. Proteomic dissection of dome formation in a mammary cell line: Role of tropomyosin-5b and maspin PNAS, May 8, 2001; 98(10): 5608 - 5613. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Rodriguez-Manzaneque, T. F. Lane, M. A. Ortega, R. O. Hynes, J. Lawler, and M. L. Iruela-Arispe Thrombospondin-1 suppresses spontaneous tumor growth and inhibits activation of matrix metalloproteinase-9 and mobilization of vascular endothelial growth factor PNAS, October 23, 2001; 98(22): 12485 - 12490. [Abstract] [Full Text] [PDF] |
||||