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a Department of Physiology and the Sam and Ann Barshop Center for Longevity and Aging Studies, University of Texas Health Science Center, San Antonio
Peter J. Hornsby, Sam and Ann Barshop Center for Longevity and Aging Studies, University of Texas Health Science Center, 15355 Lambda Drive STCBM 2.200, San Antonio, TX 78245 E-mail: hornsby{at}uthscsa.edu.
Decision Editor: James R. Smith, PhD
A long-standing controversy concerns the relevance of cellular senescence, defined and observed as a cell culture phenomenon, to tissue aging in vivo. Here the evidence on this topic is reviewed. The main conclusions are as follows. First, telomere shortening, the principal known mediator of cellular senescence, occurs in many human tissues in aging. Second, it is not clear whether this results in cellular senescence or in some other cell fate (e.g., crisis). Third, rodents probably are not appropriate experimental models for these questions, because of important differences in telomere biology between rodent cells and cells from long-lived mammals (e.g., human or bovine cells). Fourth, better and more comprehensive observations on aging human tissues are needed to answer the question of the occurrence of senescent cells in tissues, and new experimental approaches are needed to elucidate the consequences of telomere shortening in tissues in aging.
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P. J. Hornsby Aging of the Human Adrenal Cortex Sci. Aging Knowl. Environ., September 1, 2004; 2004(35): re6 - re6. [Abstract] [Full Text] [PDF] |
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J. R. Smith Author's Response to Commentary: Cell Senescence: An Evaluation of Replicative Senescence in Culture as a Model for Aging In Situ J. Gerontol. A Biol. Sci. Med. Sci., September 1, 2003; 58(9): B779 - 781. [Full Text] [PDF] |
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P. J. Hornsby Mouse and Human Cells Versus Oxygen Sci. Aging Knowl. Environ., July 30, 2003; 2003(30): pe21 - 21. [Abstract] [Full Text] |
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