Literature DB >> 21153238

Secretion of 23 kDa and glycosylated prolactin by rat pituitary cell culture in serum-free media: a comparative morphological, cyto- and immunochemical study.

F Bollengier1, M Espeel, A Matton, A Mahler, L Vanhaelst.   

Abstract

The secretion of 23 kDa prolactin by rat pituitary cells has been thoroughly investigated, but secretion of glycosylated rat prolactin is not currently known. This is mainly due to the lack of an antiserum which is solely specific for glycosylated rat prolactin and therefore we studied the basal secretion of this variant by an indirect method. Rat pituitary cells were cultured in total culture medium and three different serum-free media (DMEM, keratinocyte-serum-free medium, protein-free hybridoma medium) and secretion of 23 kDa and glycosylated rat prolactin was recorded by radioactive techniques and immunoblotting. The pituitary cell quality was monitored by electron microscopy, cell activation-and cell death assessment. In short-range culture (2 days) the pituitary cell quality and behaviour was very good and comparable in total culture medium, DMEM and keratinocyteserum-free medium, i.e. numerous secretory granules, moderate amount of ER, cristae well in place in the mitochondriae. In medium-range culture (8 days) only cells cultured in total culture medium and DMEM presented a parallel behaviour: migration of cells toward each other, marked degranulation, massive array of ER. The inner membrane of the mitochondria was no longer folded into cristae leaving an unoccupied central space. At day 2 of the culture span secretion of 23 kDa rat prolactin was very comparable in all media used; hereafter, secretion of 23 kDa rat prolactin in total culture medium and DMEM assumed the well known pattern of peaking and slowing down, whereas in the other serumfree media it steadily decreased over the culture span. Pertaining to the important novel point of glycosylated rat prolactin secretion, it was low in comparison to the one of 23 kDa rat prolactin and it assumed a near steady pattern in all media used. 26 kDa rat prolactin was identified as the preferentially secreted glycoform, and the 23 kDa isoform as the major secretory product of rat pituitary lactotroph cells.

Entities:  

Year:  1995        PMID: 21153238     DOI: 10.1007/BF02917450

Source DB:  PubMed          Journal:  Endocrine        ISSN: 1355-008X            Impact factor:   3.633


  24 in total

Review 1.  Glycosylation of pituitary hormones: a necessary and multistep control of biopotency.

Authors:  C Ronin
Journal:  Glycoconj J       Date:  1992-12       Impact factor: 2.916

Review 2.  Neuroendocrine [corrected] regulation of prolactin release.

Authors:  N Ben-Jonathan; L A Arbogast; J F Hyde
Journal:  Prog Neurobiol       Date:  1989       Impact factor: 11.685

3.  Glycoprotein synthesized by cultured cells: effects of serum concentrations and buffers on sugar content.

Authors:  J M Megaw; L D Johnson
Journal:  Proc Soc Exp Biol Med       Date:  1979-05

Review 4.  Secretion and crinophagy in prolactin cells.

Authors:  M G Farquhar
Journal:  Adv Exp Med Biol       Date:  1977       Impact factor: 2.622

5.  A novel "cleaved prolactin" in the rat pituitary: part I. Biosynthesis, characterization and regulatory control.

Authors:  I Mittra
Journal:  Biochem Biophys Res Commun       Date:  1980-08-29       Impact factor: 3.575

6.  Effect of tunicamycin, swainsonine, castanospermine, Beta-hydroxynorvaline and monensin on the post-translational processing of rat prolactin molecular forms.

Authors:  F Bollengier; B Velkeniers; A Mahler; L Vanhaelst; E Hooghe-Peters
Journal:  J Neuroendocrinol       Date:  1989-12-01       Impact factor: 3.627

7.  Further characterization of rat 26,000 prolactin as a glycoprotein with essentially o-linked carbohydrate chains.

Authors:  F Bollengier; R Hooghe; B Velkeniers; A Mahler; L Vanhaelst; E Hooghe-Peters
Journal:  J Neuroendocrinol       Date:  1991-08-01       Impact factor: 3.627

8.  Polymorphism of prolactin secreted by human prolactinoma cells: immunological, receptor binding, and biological properties of the glycosylated and nonglycosylated forms.

Authors:  I Pellegrini; G Gunz; C Ronin; E Fenouillet; J P Peyrat; P Delori; P Jaquet
Journal:  Endocrinology       Date:  1988-06       Impact factor: 4.736

9.  Rapid colorimetric assay for cell growth and survival. Modifications to the tetrazolium dye procedure giving improved sensitivity and reliability.

Authors:  F Denizot; R Lang
Journal:  J Immunol Methods       Date:  1986-05-22       Impact factor: 2.303

10.  Prolactin heterogeneity: a limitation on the evaluation of results from prolactin assays due to differences in immunoassays and the different bioactivities of prolactin forms.

Authors:  B Löhrke; S Kunkel; J Köwitz; T Viergutz; U Tiemann; H Alm; B Krüger
Journal:  Eur J Clin Chem Clin Biochem       Date:  1993-12
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