Literature DB >> 3317407

Linoleic acid, but not cortisol, stimulates accumulation of casein by mouse mammary epithelial cells in serum-free collagen gel culture.

B K Levay-Young1, G K Bandyopadhyay, S Nandi.   

Abstract

A two-step culture system has been developed to analyze the role of hormones in casein accumulation by mammary epithelial cells obtained from adrenalectomized and ovariectomized adult virgin mice. In the first step cells are grown inside collagen gel in medium containing insulin, epidermal growth factor (EGF), and linoleic acid for 9 days; these conditions stimulate very little casein accumulation. Following this growth phase the gels are released to float in medium containing insulin, prolactin, and linoleic acid. During this second phase the mammary cells will accumulate large amounts of casein, but only in the simultaneous presence of insulin, prolactin, and linoleic acid; in the absence of linoleic acid casein accumulation is greatly reduced. The casein accumulation is not dependent on the presence of the glucocorticoid cortisol and will occur in spite of the presence of the antiglucocorticoid agent RU 38 486. To determine if the response to cortisol observed in organ culture by other investigators might be mediated by stromal cells, epithelial cells were grown in collagen gel under fatty acid-free conditions and then cocultured with explants of mammary fat pads from adult virgin mice with or without mammary parenchyma. The cocultures were performed in fatty acid-free medium containing insulin and prolactin with or without cortisol. In the majority of experiments the mammary epithelial cells in the collagen gel accumulate more casein in the presence of cortisol than in its absence, irrespective of the presence of mammary parenchyma in the explant. Thus, mammary epithelial cells are directly dependent on insulin and prolactin for casein accumulation and indirectly dependent on cortisol by means of its effect on the stromal cells. This cortisol effect may be to cause release into the medium of linoleic acid or a metabolic product of linoleic acid from the stromal cells.

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Year:  1987        PMID: 3317407      PMCID: PMC299561          DOI: 10.1073/pnas.84.23.8448

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  48 in total

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Journal:  Dev Biol       Date:  1987-03       Impact factor: 3.582

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Journal:  Cancer Res       Date:  1979-02       Impact factor: 12.701

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Authors:  Q J Tonelli; S Sorof
Journal:  Differentiation       Date:  1982       Impact factor: 3.880

5.  A sensitive radioimmunoassay for a component of mouse casein.

Authors:  J Enami; S Nandi
Journal:  J Immunol Methods       Date:  1977       Impact factor: 2.303

6.  The lipolytic effects of mouse placental lactogen II, mouse prolactin, and mouse growth hormone on adipose tissue from virgin and pregnant mice.

Authors:  P J Fielder; F Talamantes
Journal:  Endocrinology       Date:  1987-08       Impact factor: 4.736

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Journal:  Science       Date:  1964-07-31       Impact factor: 47.728

8.  Insulin is essential for accumulation of casein mRNA in mouse mammary epithelial cells.

Authors:  F F Bolander; K R Nicholas; J J Van Wyk; Y J Topper
Journal:  Proc Natl Acad Sci U S A       Date:  1981-09       Impact factor: 11.205

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Authors:  S Smith; R Watts; R Dils
Journal:  J Lipid Res       Date:  1968-01       Impact factor: 5.922

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Journal:  J Cell Biol       Date:  1984-01       Impact factor: 10.539

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  8 in total

Review 1.  Three-dimensional mammary primary culture model systems.

Authors:  M M Ip; K M Darcy
Journal:  J Mammary Gland Biol Neoplasia       Date:  1996-01       Impact factor: 2.673

2.  Both cell substratum regulation and hormonal regulation of milk protein gene expression are exerted primarily at the posttranscriptional level.

Authors:  R S Eisenstein; J M Rosen
Journal:  Mol Cell Biol       Date:  1988-08       Impact factor: 4.272

3.  Primary culture of normal rat mammary epithelial cells within a basement membrane matrix. I. Regulation of proliferation by hormones and growth factors.

Authors:  H A Hahm; M M Ip
Journal:  In Vitro Cell Dev Biol       Date:  1990-08

4.  Primary culture of normal rat mammary epithelial cells within a basement membrane matrix. II. Functional differentiation under serum-free conditions.

Authors:  H A Hahm; M M Ip; K Darcy; J D Black; W K Shea; S Forczek; M Yoshimura; T Oka
Journal:  In Vitro Cell Dev Biol       Date:  1990-08

5.  Phospholipids containing polyunsaturated fatty acyl groups are mitogenic for normal mouse mammary epithelial cells in serum-free primary cell culture.

Authors:  W Imagawa; G K Bandyopadhyay; D Wallace; S Nandi
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

6.  Effect of reproductive states on lipid mobilization and linoleic acid metabolism in mammary glands.

Authors:  G K Bandyopadhyay; L Y Lee; R C Guzman; S Nandi
Journal:  Lipids       Date:  1995-02       Impact factor: 1.880

Review 7.  Diverse and active roles for adipocytes during mammary gland growth and function.

Authors:  Russell C Hovey; Lucila Aimo
Journal:  J Mammary Gland Biol Neoplasia       Date:  2010-08-19       Impact factor: 2.673

8.  The proliferation of mouse mammary epithelial cells in response to specific mitogens is modulated by the mammary fat pad in vitro.

Authors:  R C Hovey; D D MacKenzie; T B McFadden
Journal:  In Vitro Cell Dev Biol Anim       Date:  1998-05       Impact factor: 2.723

  8 in total

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