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Inverse correlation between mitochondrial size and metabolic competence: a quantitative cytochemical study of cytochrome oxidase activity

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Abstract

Mitochondria are topologically closed bilayered systems where the synthesis of adenosine triphosphate (ATP) from adenosine diphosphate (ADP) and inorganic phosphate occurs via oxidative phosphorylation. The ordered architecture (and its extension) of the mitochondria (i.e. inner membrane, outer membrane and cristae) constitutes a critical topographic arrangement for their energy-providing mechanisms. Thus, quantitative estimations of the ultrastructural features of organelles preferentially stained by means of function-related cytochemical reactions reliably report on their potential to supply adequate amounts of ATP. On the basis of this rationale, we carried out a computer-assisted cytochemical study of cytochrome oxidase (COX) activity on mitochondria of different size in the cerebellar cortex of adult rats. The total intra-mitochondrial area of the cytochemical precipitates (CPA)/mitochondrion, the area (MA) and the longer diameter (Fmax) of COX-positive organelles were measured. The ratio (R): CPA/MA was also calculated and referred to as the percentage of mitochondrial inner membrane area involved in COX activity. The regression analysis of R vs MA showed a significant inverse correlation (r=−0.905). The fourfold increase in MA from quartiles I to IV was matched by increases in Fmax and CPA, respectively, but it was also related to a 25% decrease in R. By matching quantitative cytochemical estimations of COX activity within mitochondria with the morphometric assessment of their ultrastructural features, the present study correlates size to the metabolic competence of COX-positive organelles. Quantitative cytochemistry of COX activity is currently regarded as a reliable marker of cellular metabolism; thus our findings support the hypothesis that enlargements in size are inversely correlated with the mitochondrial metabolic competence.

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References

  • Bereiter-Hahn J (1990) Behaviour of mitochondria in the living cell. Int Rev Cytol 122:1–63

    CAS  PubMed  Google Scholar 

  • Bertoni-Freddari C, Fattoretti P, Casoli T, Spagna C, Meier-Ruge W, Ulrich J (1993) Morphological plasticity of synaptic mitochondria during aging. Brain Res 628:193–200

    CAS  PubMed  Google Scholar 

  • Bertoni-Freddari C, Fattoretti P, Caselli U, Paoloni R, Meier-Ruge W (1996) Age-dependent decrease in the activity of succinic dehydrogenase in rat CA1 pyramidal cells: a quantitative cytochemical study. Mech Age Dev 90:53–62

    Article  CAS  Google Scholar 

  • Bertoni-Freddari C, Fattoretti P, Casoli T, Di Stefano G, Solazzi M, Meier-Ruge W (2001) Quantitative cytochemical mapping of mitochondrial enzymes in rat cerebella. Micron 32:405–410

    Article  CAS  PubMed  Google Scholar 

  • Coggeshall RE, Lekan HA (1996) Methods for determinating numbers of cells and synapses: a case for more uniform standards of review. J Comp Neurol 364:6–15

    Article  CAS  PubMed  Google Scholar 

  • Cruz J de la, Buron I, Roncero I (1990) Morphological and functional studies during aging at mitochondrial level: action of drugs. Int J Biochem 22:729–735

    PubMed  Google Scholar 

  • Gartner LP (1987) The fine structural morphology of the midgut of aged Drosofila: a morphometric analysis. Exp Gerontol 22:297–304

    CAS  PubMed  Google Scholar 

  • Karbowski M, Kurono C, Nishizawa Y, Horie Y, Soji T, Wakabayashi T (1997) Induction of megamitotochondria by some chemicals inducing oxidative stress in primary cultured rat hepatocytes. Biochim Biophys Acta 1349:242–250

    Article  CAS  PubMed  Google Scholar 

  • Karbowski M, Kurono C, Wozniak M, Ostrowski M, Teranishi M, Nishizawa Y, Usukura J, Soji T, Wakabayashi T (1999) Free radical-induced megamitochondria formation and apoptosis. Free Rad Biol Med 26:396–409

    Article  CAS  PubMed  Google Scholar 

  • Linnane AW, Marzuky S, Ozawa T, Tanaka M (1989) Mitochondrial DNA mutations as an important contributor to aging and degenerative diseases. Lancet:642–645

  • McCarter RJM (1995) Energy utilisation. In: Masoro EJ (ed) Handbook of physiology: aging. Oxford University Press, Oxford, pp 95–118

    Google Scholar 

  • Nakada K, Inoue K, Ono T, Isobe K, Ogura A, Goto YI, Nonaka I, Hayashi JI (2001) Inter-mitochondrial complementation: mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA. Nat Med 7:934–940

    Article  CAS  PubMed  Google Scholar 

  • Sastre J, Millan A, Garcia de la Asuncion J, Pla R, Juan G, O'Connor E, Martin JA, Drot-Lefaix MT, Vina J (1998) A ginkgo biloba extract (EGb 761) prevents mitochondrial aging by protecting against oxidative stress. Free Rad Biol Med 24:298–304

    Article  CAS  PubMed  Google Scholar 

  • Seligman AM, Karnovsky MJ, Wasserkrug HL, Hanker JS (1968) Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerising osmiophilic reagent, diaminobenzidine (DAB). J Cell Biol 38:1–14

    PubMed  Google Scholar 

  • Sohal RS, Bridges RG (1978) Associated changes in the size and number of mitochondria present in the midgut of the larvae of the housefly, Musca domestica and phospholipid composition of the larvae. J Cell Sci 34:65–79

    CAS  PubMed  Google Scholar 

  • Tauchi H, Sato T (1968) Age changes in size and number of mitochondria of human hepatic cells. J Gerontol 23:454–461

    CAS  PubMed  Google Scholar 

  • Walter PB, Beckman KB, Ames BN (1999) The role of iron and mitochondria in aging. In: Cadenas E, Packer L (eds) Understanding the process of aging: the role of mitochondria free radicals and antioxidants. Dekker, New York, pp 203–227

    Google Scholar 

  • Wong-Riley MTT (1989) Cytochrome oxidase: an endogenous metabolic marker for neuronal activity. Trends Neurosci 12:94–101

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The experiments performed in this study comply with current Italian laws.

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Correspondence to Carlo Bertoni-Freddari.

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Bertoni-Freddari, C., Fattoretti, P., Paoloni, R. et al. Inverse correlation between mitochondrial size and metabolic competence: a quantitative cytochemical study of cytochrome oxidase activity. Naturwissenschaften 90, 68–71 (2003). https://doi.org/10.1007/s00114-002-0398-8

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  • DOI: https://doi.org/10.1007/s00114-002-0398-8

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