Literature DB >> 1016244

Effect of L-azetidine-2-carboxylic acid on glycosylations of collagen in chick-embryo tendon cells.

A Oikarinen, H Anttinen, K I Kivirikko.   

Abstract

The glycosylations of hydroxylysine during collagen biosynthesis in isolated chick-embryo tendon cells were studied by using pulse-chase labelling experiments with [14C]-lysine. The hydroxylation of lysine and the glycosylations of hydroxylysine continued after a 5 min pulse label for up to about 10 min during the chase period. These data differ from those obtained previously in isolated chick-embryo cartilage cells, in which, after a similar 5 min pulse label, these reactions continued during the chase period for up to about 20 min. The collagen synthesized by the isolated chick-embryo tendon cells differed markedly from the type I collagen of adult tissues in its degree of hydroxylation of lysine residues and glycosylations of hydroxylysine residues. When the isolated tendon cells were incubated in the presence of L-azetidine-2-carboxylic acid, the degree of glycosylations of hydroxylysine during the first 10 min of the chase period was identical with that in cells incubated without thcarboxylic acid for at least 60 min, whereas no additional glycosylations took place in the control cells after the 10 min time-point. As a consequence, the collagen synthesized in the presence of this compound contained more carbohydrate than did the collagen synthesized by the control cells. Additional experiments indicated that azetidine-2-carboxylic acid did not increase the collagen glycosyltransferase activities in the tendon cells or the rate of glycosylation reactions when added directly to the enzyme incubation mixture. Control experiments with colchicine indicated that the delay in the rate of collagen secretion, which was observed in the presence of azetidine-2-carboxylic acid, did not in itself affect the degree of glycosylations of collagen. The results thus suggest that the increased glycosylations were due to inhibition of the collagen triple-helix formation, which is known to occur in the presence of azetidine-2-carboxylic acid.

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Year:  1976        PMID: 1016244      PMCID: PMC1164281          DOI: 10.1042/bj1600639

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


  35 in total

1.  Assay of collagen-galactosyltransferase and collagen-glucosyltransferase activities and preliminary characterization of enzymic reactions with transferases from chick-embryo cartilage.

Authors:  R Myllylä; L Risteli; K I Kivirikko
Journal:  Eur J Biochem       Date:  1975-04-01

2.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

Review 3.  Biosynthesis of collagen and its alterations in pathological states.

Authors:  K I Kivirikko; L Risteli
Journal:  Med Biol       Date:  1976-06

4.  The route of secretion of procollagen. The influence of alphaalpha'-bipyridyl, colchicine and antimycin A on the secretory process in embryonic-chick tendon and cartilage cells.

Authors:  R Harwood; M E Grant; D S Jackson
Journal:  Biochem J       Date:  1976-04-15       Impact factor: 3.857

5.  Formation of interchain disulfide bonds and helical structure during biosynthesis of procollagen by embryonic tendon cells.

Authors:  J D Schofield; J Uitto; D J Prockop
Journal:  Biochemistry       Date:  1974-04-23       Impact factor: 3.162

6.  Effects of temperature on conformation, hydroxylation, and secretion of chick tendon procollagen.

Authors:  S A Jimenez; M Harsch; L Murphy; J Rosenbloom
Journal:  J Biol Chem       Date:  1974-07-25       Impact factor: 5.157

7.  Purification of (14C) protocollagen and its hydroxylation by prolyl-hydroxylase.

Authors:  R A Berg; D J Prockop
Journal:  Biochemistry       Date:  1973-08-28       Impact factor: 3.162

8.  Time lag in the secretion of collagen by matrix-free tendon cells and inhibition of the secretory process by colchicine and vinblastine.

Authors:  P Dehm; D J Prockop
Journal:  Biochim Biophys Acta       Date:  1972-04-21

9.  Developmental changes in protocollagen lysyl hydroxylase activity in the chick embryo.

Authors:  L Ryhänen; K I Kivirikko
Journal:  Biochim Biophys Acta       Date:  1974-03-20

10.  Activities of prolyl hydroxylase, lysyl hydroxylase, collagen galactosyltransferase and collagen glucosyltransferase in the liver of rats with hepatic injury.

Authors:  J Risteli; K I Kivirikko
Journal:  Biochem J       Date:  1974-10       Impact factor: 3.857

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  4 in total

1.  Regulation of collagen post-translational modification in transformed human and chick-embryo cells.

Authors:  R Myllylä; K Alitalo; A Vaheri; K I Kivirikko
Journal:  Biochem J       Date:  1981-06-15       Impact factor: 3.857

2.  Abnormal type I collagen metabolism by cultured fibroblasts in lethal perinatal osteogenesis imperfecta.

Authors:  J F Bateman; T Mascara; D Chan; W G Cole
Journal:  Biochem J       Date:  1984-01-01       Impact factor: 3.857

3.  Further studies on the effect of the collagen triple-helix formation on the hydroxylation of lysine and the glycosylations of hydroxylysine in chick-embryo tendon and cartilage cells.

Authors:  A Oikarinen; H Anttinen; K I Kivirikko
Journal:  Biochem J       Date:  1977-09-15       Impact factor: 3.857

4.  Effect of prevention of procollagen triple-helix formation on proline 3-hydroxylation in freshly isolated chick-embryo tendon cells.

Authors:  K Majamaa
Journal:  Biochem J       Date:  1981-04-15       Impact factor: 3.857

  4 in total

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