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High levels of mitochondrial DNA deletions in skeletal muscle of old rhesus monkeys

  • Steven R. Schwarze
  • , Connie M. Lee
  • , Susan S. Chung
  • , Ellen B. Roecker
  • , Richard Weindruch
  • , Judd M. Aiken

Producción científica: Articlerevisión exhaustiva

115 Citas (Scopus)

Resumen

Mitochondrial DNA (mtDNA) deletions increase in abundance with age in many tissues, however, their calculated low levels (usually < 0.1%) in samples from tissue homogenates containing thousands of cells argue against physiologic significance. Through the analysis of defined numbers of cells (skeletal muscle fibers) from rhesus monkeys, we report that the calculated abundance of specific mtDNA deletions is dependent upon the number of fibers analyzed: as the number of fibers decreases, the calculated deletion abundance increases. Also, most mtDNA deletions appear to occur in a mosaic pattern, varying from cell to cell in size, number and abundance. These data support the hypothesis that mtDNA deletions can focally accumulate to high levels contributing to declines in mass and function of aging skeletal muscle.

Idioma originalEnglish
Páginas (desde-hasta)91-101
Número de páginas11
PublicaciónMechanisms of Ageing and Development
Volumen83
N.º2
DOI
EstadoPublished - sept 7 1995

Nota bibliográfica

Funding Information:
We thank the Richard Moss lab for assistance with the fiber bundle dissections, the members of our lab for helpful discussion throughout the course of this work and Drs. Debbie McKenzie, Mike Strand and Greg Cartee for criticism of the manuscript. Supported by NIH grant PO1 AGl1915 (to RW and JMA). This

Financiación

We thank the Richard Moss lab for assistance with the fiber bundle dissections, the members of our lab for helpful discussion throughout the course of this work and Drs. Debbie McKenzie, Mike Strand and Greg Cartee for criticism of the manuscript. Supported by NIH grant PO1 AGl1915 (to RW and JMA). This

FinanciadoresNúmero del financiador
National Institutes of Health (NIH)PO1 AGl1915
National Institute on AgingP01AG011915

    ASJC Scopus subject areas

    • Aging
    • Developmental Biology

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