Literature DB >> 5499970

Inner- and outer-membrane enzymes of mitochondria during liver regeneration.

A R Gear.   

Abstract

1. Marker enzymes for the mitochondrial matrix, inner membrane, inter-membrane space and outer membrane were measured in mitochondria isolated from control and regenerating rat liver. The specific activity of these enzymes was then followed for up to 30 days after operation. 2. The specific activity of marker enzymes for the matrix, inner membrane and inter-membrane space remained constant during liver regeneration. 3. However, the specific activities of monoamine oxidase and kynurenine hydroxylase, both outer-membrane markers, fell by 67% and 49% respectively from their control values at 4 days after operation, and returned to normal by about 3 weeks. 4. The repression of kynurenine hydroxylase activity was shown to be unrelated to any independent variation in tryptophan catabolism, based on tryptophan pyrrolase assays. 5. These results are considered to indicate that enzymes of the inner and outer mitochondrial membranes are synthesized asynchronously during morphogenesis. 6. The enzyme complement of purified outer membrane at 4 days after operation was about 50% of that of the appropriate control. Thus the composition of the outer membrane itself may vary dramatically, and supports the concept that constitutive enzymes may turn over independently of a membrane's existence. 7. The behaviour of the rotenone-insensitive, NADH cytochrome c reductase did not parallel the other outer-membrane enzymes for intact mitochondria, but did so when assayed in highly purified fractions of outer membrane. This suggests a labile binding to the outer membrane during the early stages of morphogenesis. 8. Electrophoresis of inner- and outer-membrane proteins revealed little difference between control and experimental mitochondria at 4 days, except for an increase in several, high-molecular-weight components of the outer membrane. These bands closely correspond to similar bands derived from smooth endoplasmic reticulum. 9. The results are discussed in relation to the biogenesis and turnover of mitochondria, and are considered to provide evidence for turnover as a unit, at least for the matrix, inner membrane, inter-membrane space and possibly some form of primary outer membrane.

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Year:  1970        PMID: 5499970      PMCID: PMC1179639          DOI: 10.1042/bj1200577

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


  29 in total

1.  Incorporation of 32P-phosphate into phosphatides of rat liver mitochondria in vivo and in vitro.

Authors:  B Kadenbach
Journal:  FEBS Lett       Date:  1968-12       Impact factor: 4.124

2.  The deletion of kynurenine hydroxylase activity during hepatocarcinogenesis.

Authors:  D E KIZER; B A HOWELL
Journal:  J Natl Cancer Inst       Date:  1963-04       Impact factor: 13.506

3.  Turnover of rat-liver mitochondria.

Authors:  M J FLETCHER; D R SANADI
Journal:  Biochim Biophys Acta       Date:  1961-08-05

4.  Tissue fractionation studies. 12. Intracellular distribution of some dehydrogenases, alkaline deoxyribonuclease and iron in rat-liver tissue.

Authors:  H BEAUFAY; D S BENDALL; P BAUDHUIN; C DE DUVE
Journal:  Biochem J       Date:  1959-12       Impact factor: 3.857

5.  Significant biochemical effects of hepatocarcinogens in the rat: a review.

Authors:  E REID
Journal:  Cancer Res       Date:  1962-05       Impact factor: 12.701

6.  Promitochondria of anaerobically grown yeast. I. Isolation and biochemical properties.

Authors:  R S Criddle; G Schatz
Journal:  Biochemistry       Date:  1969-01       Impact factor: 3.162

7.  Apparent turnover of mitochondrial deoxyribonucleic acid and mitochondrial phospholipids in the tissues of the rat.

Authors:  N J Gross; G S Getz; M Rabinowitz
Journal:  J Biol Chem       Date:  1969-03-25       Impact factor: 5.157

8.  Comparison of rat liver mitochondrial and microsomal membrane proteins.

Authors:  C A Schnaitman
Journal:  Proc Natl Acad Sci U S A       Date:  1969-06       Impact factor: 11.205

9.  Phospholipid exchange reactions within the liver cell.

Authors:  W C McMurray; R M Dawson
Journal:  Biochem J       Date:  1969-03       Impact factor: 3.857

10.  Biogenesis of endoplasmic reticulum membranes. I. Structural and chemical differentiation in developing rat hepatocyte.

Authors:  G Dallner; P Siekevitz; G E Palade
Journal:  J Cell Biol       Date:  1966-07       Impact factor: 10.539

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  9 in total

1.  Rate of restoration of cardiolipin and other major phospholipids during liver regeneration in rat.

Authors:  G Fex; K Thorzell
Journal:  Lipids       Date:  1975-05       Impact factor: 1.880

2.  Regulation of mitochondrial protein turnover by thyroid hormone(s).

Authors:  M S Rajwade; S S Katyare; P Fatterpaker; A Sreenivasan
Journal:  Biochem J       Date:  1975-11       Impact factor: 3.857

3.  Relative rates of turnover of subunits of mitochondrial proteins.

Authors:  J H Walker; R J Burgess; R J Mayer
Journal:  Biochem J       Date:  1978-12-15       Impact factor: 3.857

4.  Mitochondrial conformation and swelling-contraction reactivity during early liver regeneration.

Authors:  M A Verity; W J Brown; M Cheung
Journal:  Am J Pathol       Date:  1974-02       Impact factor: 4.307

5.  Rates of recovery of irreversibly inhibited monoamine oxidases: a measure of enzyme protein turnover.

Authors:  G Planz; K Quiring; D Palm
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1972       Impact factor: 3.000

6.  Influence of subtotal hepatectomy on peroxisomes and peroxisomal enzymes of rat liver and isolated liver cell fractions.

Authors:  H Goldenberg; M Hüttinger; P Böck; R Kramar
Journal:  Histochemistry       Date:  1975-07-16

7.  Protein degradation in rat liver during post-natal development.

Authors:  S M Russell; R J Burgess; R J Mayer
Journal:  Biochem J       Date:  1980-10-15       Impact factor: 3.857

8.  Developmental changes in mitochondria during the transition into lactation in the mouse mammary gland. II. Membrane marker enzymes and membrane ultrastructure.

Authors:  T G Rosano; S K Lee; D H Jones
Journal:  J Cell Biol       Date:  1976-06       Impact factor: 10.539

9.  Parenchymal cells from adult rat liver in nonproliferating monolayer culture. I. Functional studies.

Authors:  D M Bissell; L E Hammaker; U A Meyer
Journal:  J Cell Biol       Date:  1973-12       Impact factor: 10.539

  9 in total

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