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Involvement of Growth Factors in the Regulation of Pubertal Mammary Growth in Cattle

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Biology of the Mammary Gland

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 480))

Abstract

Pubertal mammary growth in heifers is dependent on interactions of many hormones and growth factors of which some are stimulatory while others are inhibitory. Although estrogen and growth hormone (GH) are of primary importance, more recent studies have suggested a role for both systemic and mammary tissue-specific growth factors. Growth factors may act as mediators of estrogen and GH or through specific effects of their own. These growth factors include insulin (INS), IGFs (IGF-I and IGF- II), epidermal growth factor (EGF), FGFs (FGF-1 and FGF- 2), TGFs (TGF-α and TGF-β’s, amphiregulin (AR), platelets derived growth factor (PDGF), and mammary derived growth factor-1 (MDGF-1). Using mammary epithelial cells derived from prepubertal heifers and cultured in three-dimensional collagen gels as an in vitro model, we have investigated the mitogenic effects of a number of different growth factors (IGF-I, des( 1-3) IGF-I, IGF-II, INS, EGF, TGF- α, AR, FGF-1, FGF-2, and TGF-β1). As expected, IGF-I, des(1-3)IGF-I, IGF-II and INS all stimulated proliferation of mammary cells with des( 1-3)IGF-I being the most potent and INS the least potent. The mitogenic effect of IGF-I could be inhibited by both IGFBP-2 and IGFBP-3 showing that these binding proteins modulate the bioactivity of IGF-I in the mammary gland at the cellular level. Regulation of IGF availability by IGFBPs in the extracellular environment therefore is critical for IGF action in the mammary gland. Proliferation of mammary epithelial cells was also stimulated by growth factors of the EGF family, i.e. EGF, TGF-α and AR, however, not as much as growth factors from the IGF family. Members of the fibroblast growth factor family showed various mitogenic activities. FGF-1 stimulated DNA synthesis while FGF-2 in concentrations above 10 ng/ml inhibited DNA synthesis. TGF-β1 at very low concentrations stimulated proliferation slightly whereas higher concentrations strongly inhibited proliferation of mammary epithelial cells and inhibited mitogenesis induced by growth factors of both the EGF- and IGF family. This shows that TGF-β1 is a very potent regulator of pubertal mammary growth.

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Referenes

  1. Sejrsen, K., and S. Purup. 1997. Influence of prepubertal feeding level on milk yield potential of dairy heifers: A review. J. Anim. Sci. 75, 828–835.

    Google Scholar 

  2. Forsyth IA. The mammary gland. In: Bailliere’s Clinical Endocrinology and Metabolism 5, 809–832, 1991.

    PubMed  CAS  Google Scholar 

  3. Oka T, Yoshimura M, Lavandero S, Wada K, Ohba Y. Control of growth and differentiation of the mammary gland by growth factors. J Dairy Sci 74, 2788–2800, 1991.

    PubMed  CAS  Google Scholar 

  4. Weber MS, Purup S, Vestergaard M, Ellis SE, Sondergaard J, Akers RM, Sejrsen K. Contribution of insulin-like growth factor-I (IGF-I) and IGF-binding protein-3 (IGFBP-3) to mitogenic activity in bovine mammary extracts and serum. J Endocrinology 161, 365–373, 1999.

    CAS  Google Scholar 

  5. Jones JI, Clemmons DR. Insulin-like growth factors and their binding proteins: Biological actions. Endocrine Rev 16, 3–34, 1995.

    Article  CAS  Google Scholar 

  6. Shamay, A., N. Cohen, M. Niwa, and A. Gertler. 1988. Effect of insulin-like growth factor I on deoxyribonucleic acid synthesis and galactopoiesis in bovine undifferentiated and lactating mammary tissue in vitro. Endocrinol 123, 804–809.

    Google Scholar 

  7. Peri I, Shamay A, McGrath MF, Collier RJ, Gertler A. Comparative mitogenic and galactopoietic effects of IGF-I, IGF-II and des-3-IGF-I in bovine mammary gland in vitro. Cell Biol International Reports 16, 359–368, 1992.

    CAS  Google Scholar 

  8. Forsyth IA. The insulin-like growth factor and epidermal growth factor families in mammary cell growth in ruminants: action and interaction with hormones. J Dairy Sci 79, 1085–1096, 1996.

    PubMed  CAS  Google Scholar 

  9. Collier RJ, McGrath MF, Byatt JC, Zurfluh L. Regulation of bovine mammary growth by peptide hormones: involvement of receptors, growth factors and binding proteins. Livest Prod Sci 35, 21–33, 1993.

    Article  Google Scholar 

  10. McGrath MF, Collier RJ, Clemmonds DR, Busby WH, Sweeny CA, Krivi GG. The direct in vitro effect of insulin-like growth factors (IGFs) on normal bovine mammary cell proliferation and production of IGF bindings proteins. Endocrinology 129, 671–678, 1991.

    Article  PubMed  CAS  Google Scholar 

  11. Baumrucker CR, Stemberger BM. Insulin and insulin-like growth factor-I stimulate DNA synthesis in bovine mammary tissue in vitro. J Anim Sci 67, 3503–3514, 1989.

    PubMed  CAS  Google Scholar 

  12. Purup S, Sejrsen K, Akers RM. Effect of bovine GH and ovariectomy on mammary tissue sensitivity to IGF-I in prepubertal heifers. J Endocrinol 144, 153–158, 1995.

    Article  PubMed  CAS  Google Scholar 

  13. Weber MS. The role of insulin-like growth factor-I (IGF-I) and IGF-binding proteins in mammary gland development. Ph. D. Thesis, Virginia Polytechnic Institute and State University, 1998.

    Google Scholar 

  14. Forbes B, Szabo L, Baxter RC, Ballard FC, Wallace JC. Classification of the insulin-like growth factor binding proteins with three distinct categories according to their binding specification. Biochem Biophys Res Commun 157, 196–202, 1988.

    Article  PubMed  CAS  Google Scholar 

  15. Spitzer E, Grosse R. EGF receptors on plasma membranes purified from bovine mammary gland of lactating and pregnant animals. Biochem International 14, 581–588, 1987.

    CAS  Google Scholar 

  16. Moorby CD, Taylor JA, Forsyth IA. Transforming growth factor-β: receptor binding and action on DNA synthesis in the sheep mammary gland. J Endocrinology 144, 165–171, 1995.

    Article  CAS  Google Scholar 

  17. Sheffield LG. Mastitis increases growth factor messenger ribonucleic acid in bovine mammary glands. J Dairy Sci 80, 2020–2024, 1997.

    PubMed  CAS  Google Scholar 

  18. Koff MD, Plaut K. Expression of transforming growth factor-β-like messenger ribonucleic acid transcripts in the bovine mammary gland. J Dairy Sci 78, 1903–1908, 1995.

    Article  PubMed  CAS  Google Scholar 

  19. Plath A, Einspanier R, Peters F, Sinowatz F, Schams D. Expression of transforming growth factors alpha and beta-1messenger RNA in the bovine mammary gland during different stages of development and lactation. J Endocrinol 155, 501–511, 1997.

    Article  PubMed  CAS  Google Scholar 

  20. Forsyth IA, Keable S, Taylor JA, Turvey A, Lennard S. Expression of amphiregulin in the sheep mammary gland. Mol Cell Endocrinology 126, 41–48, 1997.

    Article  CAS  Google Scholar 

  21. Shouab M, McDonald VL, Bradley G, Todaro GJ. Amphiregulin: a bifunctional growth-modulating glycoprotein produced by the phorbol 12-myristate 13-acetate-treated human breast adenocarcinoma cell line MCF-7. Proc Natl Acad Sci USA 85, 6528–6532, 1988.

    Google Scholar 

  22. Shouab M, Plowman GD, McDonald VL, Bradley JG, Todaro GJ. Structure and function of human amphiregulin: a member ofthe epidermal growth factor family. Science 243, 1074–1076, 1989.

    Google Scholar 

  23. Sheffield LG. Hormonal regulation of epidermal growth factor content and signalling in bovine mammary tissue. Endocrinology 139, 4568–75, 1998.

    Article  PubMed  CAS  Google Scholar 

  24. Zurfluh LL, Bolten SL, Byatt JC, McGrath MF, Tou JS, Zupec ME, Krivi GG. Isolation of a genomic sequence encoding a biologically active bovine TGF-α protein. Growth Factors 3, 257–266, 1990.

    Google Scholar 

  25. Forsyth IA, Taylor JA, Moorby CD. DNA synthesis by ovine mammary alveolar epithelial cells: effects of heparin, epidermal growth factor-related peptides and interaction with stage of pregnancy. J Endocrinology 156, 283–290, 1998.

    Article  CAS  Google Scholar 

  26. Collier RJ, McGrath MF. Effect of human epidermal growth factor (hEGF) on bovine mammary development in vivo. J Dairy Sci 71(Suppl.1) 228, 1988.

    Google Scholar 

  27. Woodward TL, Akers RM, Turner JD. Lack of mitogenic response to EGF, pituitary and ovarian hormones in bovine mammary epithelial cells. Endocrine 2, 529–535, 1994.

    CAS  Google Scholar 

  28. Szebenyi G, Fallon JF. Fibroblast growth factors as multifunctional signalling factors. International Rev Cytology 185, 45–106, 1999.

    CAS  Google Scholar 

  29. Plath A, Einspanier R, Gabler C, Peters F, Sinowatz F, Gospodarowicz, Schams D. Expression and localization of members of the fibroblast growth factor family in the bovinemammary gland. JDairySci 81, 2604–2613, 1998.

    CAS  Google Scholar 

  30. Levay-Young BK, Imagawa W, Wallace DR, Nandi S. Basic fibroblast growth factor stimulates the growth and inhibits casein accumulation in mouse mammary epithelial cells in vitro. Mol Cell Endocrinology 62, 327–336, 1989.

    CAS  Google Scholar 

  31. Lavandero SA, Chappuzeau A, Sapag-Hagar M, Oka T. In vivo and in vitro evidence of basic fibroblast growth factor action in mouse mammary gland development. FEBS Lett 439, 351–356, 1988.

    Google Scholar 

  32. Imagawa W, Cunha GR, Young P, Nandi S. Keratinocyte growth factor and acidic fibroblast growth factor are mitogens for primary cultures of mammary epithelium. BiochemBiophysResCommun 204, 1165–1169, 1994.

    CAS  Google Scholar 

  33. Sandowski Y, Peri I, Gertler A. Partial purification and characterization of putative paracrine/autocrine bovine mammary epithelium growthfactors. Livest ProdSci 35, 35–48, 1993.

    Google Scholar 

  34. Plaut K. Role of epidermal growth factor and transforming growth factors in mammary development and lactation. J Dairy Sci 76, 1526–1538, 1993.

    Article  PubMed  CAS  Google Scholar 

  35. Roberts AB, Sporn MB. The transforming growth factor beta. In: Peptide Growth Factors and Their receptors. MB Sporn and AB Roberts (Eds.). Springer-Verlag, Heidelberg, Germany, pp. 421–472, 1990.

    Google Scholar 

  36. Mustoe TA, Pierce GF, Thomason A, Gramates P, Sporn MB, Deuel TF. Transforming growth factor type beta induces accelerated healing of incisional wounds in rats. Science 237, 1333–1336, 1987.

    PubMed  CAS  Google Scholar 

  37. Van den Eijnden-van Raaij AJM, Koornneef I, van Zoelen EJJ. A new method for high yield purification of type beta transforming growth factor from human platelets. Biochem Biophys Res Commun 157, 16–23, 1988.

    PubMed  Google Scholar 

  38. Grainger DJ, Mosedale DE, Metcalfe JC, Weissberg PL, Kemp PR. Active and acid-activatable TGF-β in human sera, platelets and plasma. Clin Chim Acta 235, 11–31, 1995.

    Article  PubMed  CAS  Google Scholar 

  39. Purup S, Vestergaard M, Weber MS, Plaut K, Akers RM, Sejrsen K. Local regulation of pubertal mammary growth in heifers. J Anim Sci, 1999 (In press).

    Google Scholar 

  40. Plaut K, Maple RL, Capuco AV, Bell AW. Validation of transforming growth factor-(1 binding assay for bovine mammary tissue. In: Intercellular Signalling in the Mammary Gland. CJ Wilde, M Peaker, and CH Knight (Eds.), Plenum Press Ltd., 91–93, 1995.

    Google Scholar 

  41. Bano M, Salomon DS, Kidwell WR. Purification of a mammary-derived growth factor from human milk and human mammary tumors. J Biol Chem 260, 5745–5752, 1985.

    PubMed  CAS  Google Scholar 

  42. Bano M, Kidwell WR, Lippman ME, Dickson RB. Characterization of mammary-derived growth factor-1 receptors and response in human mammary epithelial cell lines. J Biol Chem 265, 1874–1880, 1990.

    PubMed  CAS  Google Scholar 

  43. Bronzert DA, Bates SE, Sheridan JP. Transforming growth factor-( induces platelet-derived growth factor (PDGF) messenger RNA and PDGF secretion while inhibiting growth in normal human mammary epithelial cells. Mol Endocrinology 4, 981–989, 1990.

    CAS  Google Scholar 

  44. Rozengurt E, Sinnet-Smith J, Taylor-Papadimitriou J. Production of PDGF-like growth factor by breast cancer cell lines. International J Cancer 36, 247–252, 1985.

    Article  CAS  Google Scholar 

  45. Politis I, Fantuz F, Baldi A. Identification of mammary-derived growth inhibitor in sheep mammary tissue. Small Ruminant Res 18, 151–155, 1995.

    Article  Google Scholar 

  46. Bóhmer FD, Kraft R, Otto A, Wernstedt C, Hellman U, Kurtz A, Muller T, Rohdi K, Etzold G, Lehmann W. Identification of a polypeptide growth inhibitor from bovine mammary gland. J Biol Chem 262, 15137–15143, 1987

    PubMed  Google Scholar 

  47. Kurtz A, Vogel F, Funa K, Heldin CH, Grosse R. Developmental regulation of mammary-derived growth inhibitor expression in bovine mammary tissue. J Cell Biol 110, 1779–1789, 1990.

    Article  PubMed  CAS  Google Scholar 

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© 2002 Kluwer Academic Publishers

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Purup, S., Vestergaard, M., Sejrsen, K. (2002). Involvement of Growth Factors in the Regulation of Pubertal Mammary Growth in Cattle. In: Mol, J.A., Clegg, R.A. (eds) Biology of the Mammary Gland. Advances in Experimental Medicine and Biology, vol 480. Springer, Boston, MA. https://doi.org/10.1007/0-306-46832-8_4

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  • DOI: https://doi.org/10.1007/0-306-46832-8_4

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-306-46414-0

  • Online ISBN: 978-0-306-46832-2

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