Literature DB >> 6468521

High-voltage electron microscopy of human diploid fibroblasts during ageing in vitro. Morphometric analysis of mitochondria.

S Goldstein, E J Moerman, K Porter.   

Abstract

Since recent studies have suggested a diminished mitochondrial functional capacity in late-passage ('old') compared to early-passage ('young') normal fibroblasts and fibroblasts from the Hutchinson-Gilford (progeria) syndrome of premature ageing, we analysed whole-cell preparations on the high voltage electron microscope to look for mitochondrial and related defects. All strains examined showed considerable heterogeneity in cell size and intracellular morphology. Mitochondria were readily seen in all cells, predominantly as long slender rods with frequent branching, but occasional circular and saccular forms were also evident. Various parameters of mitochondrial mass including mean number, weight, and total length of mitochondria per cell weight tended to increase in old and progeria cells, but only the former attained statistical significance due to the heterogeneity and consequent variance. A significant finding was the decreased width of mitochondria in old and progeria cells. Cystic blebs were evident in mitochondria of some cells with an apparent increase in old and progeria fibroblasts. These blebs appeared to be due to weakening of the inner membrane, allowing dilatation of the outer membrane which otherwise appeared intact. The number of osmiophilic inclusions per cell weight, particularly lipofuscin granules and autophagic vacuoles, was significantly increased in old and progeria cells. In conclusion, despite some morphological changes, mitochondria of old and progeria cells maintain a structurally and bioenergetically adequate mass compatible with continued cellular viability.

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Mesh:

Year:  1984        PMID: 6468521     DOI: 10.1016/0014-4827(84)90671-2

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  8 in total

Review 1.  A comparative analysis of the cell biology of senescence and aging.

Authors:  Eun Seong Hwang; Gyesoon Yoon; Hyun Tae Kang
Journal:  Cell Mol Life Sci       Date:  2009-05-07       Impact factor: 9.261

2.  Division of mitochondria in cultured human fibroblasts.

Authors:  Hisashi Fujioka; Bernard Tandler; Mary C Consolo; Pratima Karnik
Journal:  Microsc Res Tech       Date:  2013-09-05       Impact factor: 2.769

3.  Novel roles for actin in mitochondrial fission.

Authors:  Anna L Hatch; Pinar S Gurel; Henry N Higgs
Journal:  J Cell Sci       Date:  2014-09-12       Impact factor: 5.285

4.  Distinctive gene expression patterns in human mammary epithelial cells and breast cancers.

Authors:  C M Perou; S S Jeffrey; M van de Rijn; C A Rees; M B Eisen; D T Ross; A Pergamenschikov; C F Williams; S X Zhu; J C Lee; D Lashkari; D Shalon; P O Brown; D Botstein
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

5.  Oxidative DNA damage and senescence of human diploid fibroblast cells.

Authors:  Q Chen; A Fischer; J D Reagan; L J Yan; B N Ames
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

6.  Senescence-associated changes in respiration and oxidative phosphorylation in primary human fibroblasts.

Authors:  Eveline Hutter; Kathrin Renner; Gerald Pfister; Petra Stöckl; Pidder Jansen-Dürr; Erich Gnaiger
Journal:  Biochem J       Date:  2004-06-15       Impact factor: 3.857

7.  Glycogen Synthase Kinase 3 Inactivation Induces Cell Senescence through Sterol Regulatory Element Binding Protein 1-Mediated Lipogenesis in Chang Cells.

Authors:  You-Mie Kim; Insun Song; Yong-Hak Seo; Gyesoon Yoon
Journal:  Endocrinol Metab (Seoul)       Date:  2013-12-12

8.  Multiple dynamin family members collaborate to drive mitochondrial division.

Authors:  Jason E Lee; Laura M Westrate; Haoxi Wu; Cynthia Page; Gia K Voeltz
Journal:  Nature       Date:  2016-10-31       Impact factor: 49.962

  8 in total

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