Literature DB >> 518567

Casein turnover in rabbit mammary explants in organ culture.

K Al-Sarraj, J Newbury, D A White, R J Mayer.   

Abstract

1. Explants of mammary gland from mid-pregnant rabbits were cultured in medium 199 containing insulin, prolactin and cortisol, and specific anti-casein immunoglobulin G was used to measure the amount, rate of synthesis and rate of degradation of casein in the explants in the presence of hormones and after removal of hormones from previously stimulated tissue. 2. The amount of casein in particle-free supernatants prepared from mammary explants was measured by ;rocket' immunoelectrophoresis. 3. The rate of incorporation of l-[4,5-(3)H]leucine into casein was measured after isolation of the casein by immunoadsorbent chromatography and polyacrylamide-gel electrophoresis in the presence of urea and sodium dodecyl sulphate. 4. Casein accumulates in mammary explants in the presence of insulin, prolactin and cortisol, but not in the absence of hormones. Removal of hormones after 24h in culture results in a decrease in the rate of accumulation of casein in the explants. 5. Casein-synthetic rate increases in mammary explants in the presence of insulin, prolactin and cortisol, but not in the absence of hormones. Removal of hormones after 24h in culture results in continued casein synthesis at approx. 30% of the rate in the presence of hormones. The synthetic rate does not decrease to values observed in explants cultured throughout in the absence of hormones. 6. Casein is not degraded in mammary explants during a phase of rapid casein accumulation (36-72h) in the presence of hormones. Furthermore casein is not degraded when hormones are removed from the tissue after between 36 and 72h in culture. 7. Casein is glycosylated in mammary explants; the extent of glycosylation parallels the rate of synthesis. The glycosylated protein is rapidly secreted from the tissue. 8. The results are consistent with the notion that after hormonal stimulation mammary explants from mid-pregnant rabbits synthesize, glycosylate and rapidly secrete casein. Removal of hormones decreases the synthetic rate of casein, but does not cause the accumulation of a pool of degradable casein in the lobuloalveolar cells.

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Year:  1979        PMID: 518567      PMCID: PMC1161419          DOI: 10.1042/bj1820837

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  24 in total

1.  Immunochemical characterization of casein from rabbit mammary gland.

Authors:  K Al-Sarraj; D A White; R J Mayer
Journal:  Biochem J       Date:  1978-09-01       Impact factor: 3.857

2.  Nutrition of animal cells in tissue culture; initial studies on a synthetic medium.

Authors:  J F MORGAN; H J MORTON; R C PARKER
Journal:  Proc Soc Exp Biol Med       Date:  1950-01

Review 3.  Responses of mammary cells to hormones.

Authors:  M R Banerjee
Journal:  Int Rev Cytol       Date:  1976

4.  Stabilization of casein mRNA by prolactin and glucocorticoids.

Authors:  L M Houdebine; E Devinoy; C Delouis
Journal:  Biochimie       Date:  1978       Impact factor: 4.079

5.  A method for the analysis of protein turnover characteristics. Indirect estimation of rates of protein degradation.

Authors:  N Paskin; R J Mayer
Journal:  Biochem J       Date:  1978-07-15       Impact factor: 3.857

6.  Effects of glucocorticoids on casein gene expression in the rabbit.

Authors:  E Devinoy; L M Houdebine
Journal:  Eur J Biochem       Date:  1977-05-16

7.  Guinea-pig milk-protein synthesis. Isolation and characterization of messenger ribonucleic acids from lactating mammary gland and identification of caseins and pre-alpha-lactalbumin as translation products in heterologous cell-free systems.

Authors:  R K Craig; P A Brown; O S Harrison; D McIlreavy; P N Campbell
Journal:  Biochem J       Date:  1976-10-15       Impact factor: 3.857

8.  Quantitation of casein messenger ribonucleic acid sequences using a specific complementary DNA hybridization probe.

Authors:  J M Rosen; S W Barker
Journal:  Biochemistry       Date:  1976-11-30       Impact factor: 3.162

9.  The formation of lipid-linked sugars as intermediates in glycoprotein synthesis in rabbit mammary gland.

Authors:  B K Speake; D A White
Journal:  Biochem J       Date:  1978-02-15       Impact factor: 3.857

10.  Hormone-inducible casein messenger RNA in a serum-free organ culture of whole mammary gland.

Authors:  P M Terry; M R Banerjee; R M Lui
Journal:  Proc Natl Acad Sci U S A       Date:  1977-06       Impact factor: 11.205

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  5 in total

1.  Protein degradation during terminal cytodifferentiation. Studies on mammary gland in organ culture.

Authors:  C J Wilde; N Paskin; J Saxton; R J Mayer
Journal:  Biochem J       Date:  1980-10-15       Impact factor: 3.857

2.  Prolactin-induced alpha-lactalbumin activity in mammary explants from pregnant rabbits. A role for epidermal growth factor and glucocorticoids.

Authors:  L Sankaran; Y J Topper
Journal:  Biochem J       Date:  1984-02-01       Impact factor: 3.857

3.  Extensive destruction of newly synthesized casein in mammary explants in organ culture.

Authors:  H Razooki Hasan; D A White; R J Mayer
Journal:  Biochem J       Date:  1982-01-15       Impact factor: 3.857

4.  Glycoprotein synthesis in explants of developing rabbit mammary gland in culture.

Authors:  J P Bradshaw; D A White
Journal:  Biochem J       Date:  1981-09-15       Impact factor: 3.857

5.  TGF beta suppresses casein synthesis in mouse mammary explants and may play a role in controlling milk levels during pregnancy.

Authors:  S D Robinson; A B Roberts; C W Daniel
Journal:  J Cell Biol       Date:  1993-01       Impact factor: 10.539

  5 in total

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