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 thus creates 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 in damage, but a matter of failure to replace it due to a 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 originate 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
editSome of the proponents of this theory have been Norman E. Sharpless, Ronald A. DePinho, Huber Warner, Alessandro Testori [2] and others. Warner came to this conclusion after analyzing human case of Hutchinson's Gilford syndrome and mouse models of accelerated aging.
Stem cells will turn into certain cells as the body needs them. 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.[3]
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.[4]
Recent work has suggested that, although adult tissue stem cells may the key cell type in the aging process, they may contribute via reducing their differentiation rates, rather than via becoming exhausted. Under this model, when stem cells divide but do not differentiate, they produce an excess of daughter stem cells. This phenotype will be selected for, at the cellular level, if it is caused by heritable epigenetic changes or genetic mutations, and has the potential to overwhelm homeostatic regulation of cell numbers when organismal integrity is under reduced selection in later life.[5]
Behrens et al.[6] 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
editHematopoietic stem cells (HSCs) regenerate the blood system throughout life and maintain homeostasis.[7] DNA strand breaks accumulate in long term HSCs during aging.[8][9] This accumulation is associated with a broad attenuation of DNA repair and response pathways that depends on HSC quiescence.[9] 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.[10] These findings suggest that NHEJ is a key determinant of the ability of HSCs to maintain themselves over time.[10]
Hematopoietic stem cell diversity aging
editA study showed that the clonal diversity of stem cells that produce blood cells gets drastically reduced around age 70 to a faster-growing few, substantiating a novel theory of ageing which could enable healthy aging.[11][12]
Hematopoietic mosaic loss of chromosome Y
editA 2022 study showed that blood cells' loss of the Y chromosome in a subset of cells, called 'mosaic loss of chromosome Y' (mLOY) and reportedly affecting at least 40% of 70 years-old men to some degree, contributes to fibrosis, heart risks, and mortality in a causal way.[13][14]
Hair follicle stem cell aging
editA key aspect of hair loss with age is the aging of the hair follicle.[15] 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.[16] 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.[citation needed]
Evidence against the theory
editDiseases 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. Aplastic Anemia is often an adverse effect of certain medications [17] but as such it cannot really be considered as evidence against the stem cell theory of aging. The cellularity of the bone marrow does decrease with age and can be usually calculated by the formula 100-age, and this seems consistent with a stem cell theory of aging.[18] 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.[19]
Other theories of aging
editThe 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 theories of ageing include phenomena such as gene regulation (gene expression), codon restriction, error catastrophe, somatic mutation, accumulation of genetic material (DNA) damage (DNA damage theory of aging) and dysdifferentiation. 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.[citation needed]
Footnotes
edit- ^ 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.
- ^ Mayo Clin Proc. 2018 Nov;93(11):1684-1685
- ^ Wallenfang MR, Nayak R, DiNardo S (2006). "Dynamics of the male germline stem cell population during aging of Drosophila melanogaster". Aging Cell. 5 (4): 297–304. doi:10.1111/j.1474-9726.2006.00221.x. PMID 16800845. S2CID 23514768.
- ^ Rota M, LeCapitaine N, Hosoda T, Boni A, De Angelis A, Padin-Iruegas M, Esposito G, Vitale S, Urbanek K, Casarsa C, Giorgio M, Luscher T, Pelicci P, Anversa P, Leri A, Kajstura J (2006). "Diabetes Promotes Cardiac Stem Cell Aging and Heart Failure, Which Are Prevented by Deletion of the p66shc Gene". Circ. Res. 99 (1): 42–52. doi:10.1161/01.RES.0000231289.63468.08. PMID 16763167.
- ^ Bodmer F, Crouch DJ (2020). "Somatic selection of poorly differentiating variant stem cell clones could be a key to human ageing". Journal of Theoretical Biology. 489: 110153. Bibcode:2020JThBi.48910153B. doi:10.1016/j.jtbi.2020.110153. PMID 31935413. S2CID 210814272.
- ^ 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.
- ^ Mahla RS (2016). "Stem cells application in regenerative medicine and disease threpeutics". International Journal of Cell Biology. 2016 (7): 19. doi:10.1155/2016/6940283. PMC 4969512. PMID 27516776.
- ^ 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. Bibcode:2007Natur.447..725R. doi:10.1038/nature05862. PMID 17554309. S2CID 4416445.
- ^ 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.
- ^ 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. Bibcode:2007Natur.447..686N. doi:10.1038/nature05875. PMID 17554302. S2CID 4332976.
- ^ "Research may reveal why people can suddenly become frail in their 70s". The Guardian. 1 June 2022. Retrieved 18 July 2022.
- ^ Mitchell, Emily; Spencer Chapman, Michael; Williams, Nicholas; Dawson, Kevin J.; Mende, Nicole; Calderbank, Emily F.; Jung, Hyunchul; Mitchell, Thomas; Coorens, Tim H. H.; Spencer, David H.; Machado, Heather; Lee-Six, Henry; Davies, Megan; Hayler, Daniel; Fabre, Margarete A.; Mahbubani, Krishnaa; Abascal, Federico; Cagan, Alex; Vassiliou, George S.; Baxter, Joanna; Martincorena, Inigo; Stratton, Michael R.; Kent, David G.; Chatterjee, Krishna; Parsy, Kourosh Saeb; Green, Anthony R.; Nangalia, Jyoti; Laurenti, Elisa; Campbell, Peter J. (June 2022). "Clonal dynamics of haematopoiesis across the human lifespan". Nature. 606 (7913): 343–350. Bibcode:2022Natur.606..343M. doi:10.1038/s41586-022-04786-y. ISSN 1476-4687. PMC 9177428. PMID 35650442.
- ^ Kolata, Gina (14 July 2022). "As Y Chromosomes Vanish With Age, Heart Risks May Grow". The New York Times. Retrieved 21 August 2022.
- ^ Sano, Soichi; Horitani, Keita; Ogawa, Hayato; Halvardson, Jonatan; Chavkin, Nicholas W.; Wang, Ying; Sano, Miho; Mattisson, Jonas; Hata, Atsushi; Danielsson, Marcus; Miura-Yura, Emiri; Zaghlool, Ammar; Evans, Megan A.; Fall, Tove; De Hoyos, Henry N.; Sundström, Johan; Yura, Yoshimitsu; Kour, Anupreet; Arai, Yohei; Thel, Mark C.; Arai, Yuka; Mychaleckyj, Josyf C.; Hirschi, Karen K.; Forsberg, Lars A.; Walsh, Kenneth (15 July 2022). "Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality". Science. 377 (6603): 292–297. Bibcode:2022Sci...377..292S. doi:10.1126/science.abn3100. ISSN 0036-8075. PMC 9437978. PMID 35857592.
- ^ Lei M, Chuong CM (2016). "STEM CELLS. Aging, alopecia, and stem cells". Science. 351 (6273): 559–60. Bibcode:2016Sci...351..559L. doi:10.1126/science.aaf1635. PMID 26912687.
- ^ 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. S2CID 5078019.
- ^ "Aplastic Anemia | NHLBI, NIH". Nhlbi.nih.gov. 18 January 2019. Retrieved 19 February 2022.
- ^ "Bone Marrow in Aging: Changes? Yes; Clinical Malfunction? Not So Clear". Archived from the original on 9 December 2018.
- ^ Liang Y, Zant G (2008). "Aging stem cells, latexin, and longevity". Experimental Cell Research. 314 (9): 1962–1972. doi:10.1016/j.yexcr.2008.01.032. PMC 2471873. PMID 18374916.
References
edit- Sharpless NE, DePinho RA (2004). "Telomeres, stem cells, senescence, and cancer". J. Clin. Invest. 113 (2): 160–168. doi:10.1172/JCI200420761. PMC 311439. PMID 14722605.
- 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 (1): 88–100. doi:10.1101/gad.1029903. PMC 195968. PMID 12514102.
- Metcalfe JA, et al. (1996). "Accelerated telomere shortening in ataxia telangiectasia". Nat. Genet. 13 (3): 350–353. doi:10.1038/ng0796-350. PMID 8673136. S2CID 22667293.
- Hastie ND, et al. (1990). "Telomere reduction in human colorectal carcinoma and with ageing". Nature. 346 (6287): 866–868. Bibcode:1990Natur.346..866H. doi:10.1038/346866a0. PMID 2392154. S2CID 4258451.
- Allsopp RC, et al. (1992). "Telomere length predicts replicative capacity of human fibroblasts". Proc. Natl. Acad. Sci. U.S.A. 89 (21): 10114–10118. Bibcode:1992PNAS...8910114A. doi:10.1073/pnas.89.21.10114. PMC 50288. PMID 1438199.
- 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 (10): 5607–5610. Bibcode:1998PNAS...95.5607F. doi:10.1073/pnas.95.10.5607. PMC 20425. PMID 9576930.
- 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. 8 (4): 439–448. doi:10.1111/j.1474-9726.2009.00489.x. PMC 2752333. PMID 19485966.
- Warner HR (November 2007). "Kent award lecture: is cell death and replacement a factor in aging?". J Gerontol A Biol Sci Med Sci. 62 (11): 1228–32. doi:10.1093/gerona/62.11.1228. PMID 18000142.
- 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. PMID 15378089.
- Weinert BT, Timiras PS (2003). "Invited Review: Theories of Aging". J Appl Physiol. 95 (4): 1706–1716. doi:10.1152/japplphysiol.00288.2003. PMID 12970376.
- Kirkwood TB (February 2005). "Understanding the Odd Science of Aging". Cell. 120 (4): 437–447. doi:10.1016/j.cell.2005.01.027. PMID 15734677. S2CID 7514614.
- 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. PMC 3257978. PMID 21540846.
- Smith JA, Daniel R (June 2012). "Stem Cells and Aging: A Chicken-Or-Egg Issue?". Aging and Disease. 3 (3): 260–268. PMC 3375082. PMID 22724084.
- Liang Y, Zant GV (2008). "Aging stem cells, latexin, and longevity". Experimental Cell Research. 314 (9): 1962–1972. doi:10.1016/j.yexcr.2008.01.032. PMC 2471873. PMID 18374916.
- Zant GV, Liang Y (2003). "The role of stem cells in aging". Experimental Hematology. 31 (8): 659–672. doi:10.1016/S0301-472X(03)00088-2. PMID 12901970.
- Rao MS, Mattson MP (2001). "Stem cells and aging: expanding the possibilities". Mechanisms of Ageing and Development. 122 (7): 713–734. doi:10.1016/s0047-6374(01)00224-x. PMID 11322994. S2CID 32096146.
- 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 (1): 162–166. doi:10.1046/j.1365-2141.1999.01477.x. PMID 10444180.