Jump to content

Stem cell theory of aging

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by 86.154.102.103 (talk) at 20:02, 1 September 2016 (updated link). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

The stem cell theory of aging postulates that the aging process is the result of the inability of various types of stem cells to continue to replenish the tissues of an organism with functional differentiated cells capable of maintaining that tissue's (or organ's) original function. Damage and error accumulation in genetic material is always a problem for systems regardless of the age. The number of stem cells in young people is very much higher than older people and this cause a better and more efficient replacement mechanism in the young contrary to the old. In other words, aging is not a matter of the increase of damage, but a matter of failure to replace it due to decreased number of stem cells. Stem cells decrease in number and tend to lose the ability to differentiate into progenies or lymphoid lineages and myeloid lineages.

Maintaining the dynamic balance of stem cell pools requires several conditions. Balancing proliferation and quiescence along with homing (See niche) and self-renewal of hematopoietic stem cells are favoring elements of stem cell pool maintenance while differentiation, mobilization and senescence are detrimental elements. These detrimental effects will eventually cause apoptosis.

There are also several challenges when it comes to therapeutic use of stem cells and their ability to replenish organs and tissues. First, different cells may have different lifespans even though they are originated from the same stem cells (See T-cells and erythrocytes), meaning that aging can occur differently in cells that have longer lifespans as opposed to the ones with shorter lifespans. Also, continual effort to replace the somatic cells may cause exhaustion of stem cells.[1]

Research

Some of the proponents of this theory have been Norman E. Sharpless, Ronald A. DePinho, Huber Warner, Alessandro Testori and others. Warner came to this conclusion after analyzing human case of Hutchinson's Gilford syndrome and mouse models of accelerated aging.

Stem cells divide more than non stem cells so the tendency of accumulating damage is greater. Although they have protective mechanisms, they still age and lose function. Matthew R. Wallenfang, Renuka Nayak and Stephen DiNardo showed this in their study. According to their findings, it is possible to track male GSCs labeled with lacZ gene in Drosophila model by inducing recombination with heat shock and observe the decrease in GSC number with aging. In order to mark GSCs with lacZ gene, flip recombinase (Flp)-mediated recombination is used to combine a ubiquitously active tubulin promoter followed by an FRT (flip recombinase target) site with a promotorless lacZ ORF (open reading frame) preceded by an FRT site. Heat shock is used to induce Flp recombinase marker gene expression is activated in dividing cells due to recombination. Consequently, all clone of cells derived from GSC are marked with a functional lacZ gene. By tracking the marked cells, they were able to show that GSCs do age.[2]

Another study in a mouse model shows that stem cells do age and their aging can lead to heart failure. Findings of the study indicate that diabetes leads to premature myocyte senescence and death and together they result in the development of cardiomyopathy due to decreased muscle mass.[3]

Behrens et al.[4] have reviewed evidence that age-dependent accumulation of DNA damage in both stem cells and cells that comprise the stem cell microenvironment is responsible, at least in part, for stem cell dysfunction with aging.

Hematopoietic stem cell aging

Hematopoietic stem cells (HSCs) regenerate the blood system throughout life and maintain homeostasis. DNA strand breaks accumulate in long term HSCs during aging.[5][6] This accumulation is associated with a broad attenuation of DNA repair and response pathways that depends on HSC quiescence.[6] DNA ligase 4 (Lig4) has a highly specific role in the repair of double-strand breaks by non-homologous end joining (NHEJ). Lig4 deficiency in the mouse causes a progressive loss of HSCs during aging.[7] These findings suggest that NHEJ is a key determinant of the ability of HSCs to maintain themselves over time.[7]

Hair follicle stem cell aging

A key aspect of hair loss with age is the aging of the hair follicle.[8] Ordinarily, hair follicle renewal is maintained by the stem cells associated with each follicle. Aging of the hair follicle appears to be primed by a sustained cellular response to the DNA damage that accumulates in renewing stem cells during aging.[9] This damage response involves the proteolysis of type XVII collagen by neutrophil elastase in response to the DNA damage in the hair follicle stem cells. Proteolysis of collagen leads to elimination of the damaged cells and then to terminal hair follicle miniaturization.

Evidence against the theory

Diseases such as Alzheimer's disease, end-stage renal failure and heart disease are caused by different mechanisms that are not related to stem cells. Also, some diseases related to hematopoietic system, such as aplastic anemia and complete bone marrow failure, are not especially age-dependent. Moreover, a dog study published by Zaucha J.M, Yu C. and Mathioudakis G., et al. also shows evidence against the stem cell theory. Experimental comparison of the engraftment properties of young and old marrow in a mammal model, the dog, failed to show any decrement in stem cell function with age.[10]

Other theories of aging

The aging process can be explained with different theories. These are evolutionary theories, molecular theories, system theories and cellular theories. The evolutionary theory of ageing was first proposed in the late 1940s and can be explained briefly by the accumulation of mutations (evolution of ageing), disposable soma and antagonistic pleiotropy hypothesis. The molecular theory of ageing includes phenomena such as gene regulation (gene expression), codon restriction, error catastrophe, somatic mutation (accumulation of genetic material damage) and dysdifferentiation (DNA damage theory of aging). The system theories include the immunologic approach to ageing, rate-of-living and the alterations in neuroendocrinal control mechanisms. (See homeostasis). Cellular theory of ageing can be categorized as telomere theory, free radical theory (free-radical theory of aging) and apoptosis. The stem cell theory of aging is also a sub-category of cellular theories.

Footnotes

  1. ^ Smith J., A., Daniel R. "Stem Cells and Aging: A Chicken-Or-Egg Issue?". Aging and Disease. 2012 Jun, Vol. 3, Number 3; 260–268.
  2. ^ Wallenfang M. R., Nayak R. & DiNardo S. Aging Cell (2006) 5, pp297-304. doi:10.1111/j.1474-9726.2006.0221.x
  3. ^ Rota M., LeCapitaine N., Hosoda T., Boni A., De Angelis A., Padin-Iruegas M., E., Esposito G., Vitale S., Urbanek K., Casarsa C., Giorgio M., Luscher T., F., Pelicci P., G., Anversa P., Leri A., Kajstura J. Diabetes Promotes Cardiac Stem Cell Aging and Heart Failure, Which Are Prevented by Deletion of the p66shc Gene. Circ res. 2006;99:42-52. doi:10.1161/01.RES.0000231289.63468.08
  4. ^ Behrens A, van Deursen JM, Rudolph KL, Schumacher B (2014). "Impact of genomic damage and ageing on stem cell function". Nat. Cell Biol. 16 (3): 201–7. doi:10.1038/ncb2928. PMC 4214082. PMID 24576896.
  5. ^ Rossi DJ, Bryder D, Seita J, Nussenzweig A, Hoeijmakers J, Weissman IL (2007). "Deficiencies in DNA damage repair limit the function of haematopoietic stem cells with age". Nature. 447 (7145): 725–9. doi:10.1038/nature05862. PMID 17554309.
  6. ^ a b Beerman I, Seita J, Inlay MA, Weissman IL, Rossi DJ (2014). "Quiescent hematopoietic stem cells accumulate DNA damage during aging that is repaired upon entry into cell cycle". Cell Stem Cell. 15 (1): 37–50. doi:10.1016/j.stem.2014.04.016. PMC 4082747. PMID 24813857.
  7. ^ a b Nijnik A, Woodbine L, Marchetti C, Dawson S, Lambe T, Liu C, Rodrigues NP, Crockford TL, Cabuy E, Vindigni A, Enver T, Bell JI, Slijepcevic P, Goodnow CC, Jeggo PA, Cornall RJ (2007). "DNA repair is limiting for haematopoietic stem cells during ageing". Nature. 447 (7145): 686–90. doi:10.1038/nature05875. PMID 17554302.
  8. ^ Lei M, Chuong CM (2016). "STEM CELLS. Aging, alopecia, and stem cells". Science. 351 (6273): 559–60. doi:10.1126/science.aaf1635. PMID 26912687.
  9. ^ Matsumura H, Mohri Y, Binh NT, Morinaga H, Fukuda M, Ito M, Kurata S, Hoeijmakers J, Nishimura EK (2016). "Hair follicle aging is driven by transepidermal elimination of stem cells via COL17A1 proteolysis". Science. 351 (6273): aad4395. doi:10.1126/science.aad4395. PMID 26912707.
  10. ^ Liang Y., Zant G., V. 2008. "Aging stem cells, latexin, and longevity". Experimental Cell Research 314 doi:10.1016/j.yescr.2008.01.032

References

  • Sharpless N.E., DePinho, R. A. Telomeres, stem cells, senescence, and cancer. J. Clin. Invest. 113:160–168 (2004). doi:10.1172/JCI200420761.
  • Chang S, Khoo CM, Naylor ML, Maser RS, DePinho RA (2003). "Telomere-based crisis: functional differences between telomerase activation and ALT in tumor progression". Genes Dev. 17: 88–100. doi:10.1101/gad.1029903.
  • Metcalfe JA, et al. (1996). "Accelerated telomere shortening in ataxia telangiectasia". Nat. Genet. 13: 350–353. doi:10.1038/ng0796-350.
  • Hastie ND, et al. (1990). "Telomere reduction in human colorectal carcinoma and with ageing". Nature. 346: 866–868. doi:10.1038/346866a0.
  • Allsopp RC, et al. (1992). "Telomere length predicts replicative capacity of human fibroblasts". Proc. Natl. Acad. Sci. U.S.A. 89: 10114–10118.
  • Frenck RW Jr, Blackburn EH, Shannon KM (1998). "The rate of telomere sequence loss in human leukocytes varies with age". Proc. Natl. Acad. Sci. U.S.A. 95: 5607–5610. doi:10.1073/pnas.95.10.5607.
  • Liu, Y., Sanoff, H., Cho, H., Burd, C., Torrice, C., Ibrahim, J., Thomas, N., & Sharpless, N. (2009). Expression of p16INK4a in peripheral blood T-cells is a biomarker of human aging Aging Cell doi:10.1111/j.1474-9726.2009.00489.x
  • Warner HR (Nov 2007). "Kent award lecture: is cell death and replacement a factor in aging?". J Gerontol A Biol Sci Med Sci. 62 (11): 1228–32.
  • Bell DR, Van Zant G (2004). "Stem cells, ageing, and cancer: Inevitabilities and outcomes". Oncogene. 23 (43): 7290–7296. doi:10.1038/sj.onc.1207949.
  • Weinert, B. T., Timiras, P. S. Invited Review: Theories of Aging. J Appl Physiol 95:1706-1716, 2003. doi:10.1152/japplphysiol.0028.2003.
  • Kirkwood, T. B. L. Understanding the Odd Science of Aging. Cell. 2005 Feb; Vol.120,437-447. doi:10.1016/j.cell.2005.01.027.
  • Jones DL, et al. (May 2011). "Emerging Models and Paradigms for stem cell ageing". Nat Cell Biol. 13 (5): 506–512. doi:10.1038/ncb0511-506.
  • Smith JA, Daniel R (Jun 2012). "Stem Cells and Aging: A Chicken-Or-Egg Issue?". Aging and Disease. 3 (3): 260–268.
  • Liang Y, Zant GV (2008). "Aging stem cells, latexin, and longevity". Experimental Cell Research. doi:10.1016/j.yescr.2008.01.032.
  • Zant GV, Liang Y (2003). "The role of stem cells in aging". Experimental Hematology. 31: 659–672. doi:10.1016/S0301-472X(03)00088-2.
  • Rao MS, Mattson MP (2001). "Stem cells and aging: expanding the possibilities". Mechanisms of Ageing and Development. 122: 713–734. doi:10.1016/s0047-6374(01)00224-x.
  • Marley SB, Lewis JL, Davidson RJ, et al. (1999). "Evidence for a continuous decline in hematopietic cell function from birth: application to evaluating bone marrow failure in children". Br J Haematol. 106: 162–166. doi:10.1046/j.1365-2141.1999.01477.x.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Stem_cell_theory_of_aging&oldid=737283541"