Cited by 19Neuroinflammation and Neurodegeneration MechanismsTelomeres, Telomerase, and SenescenceGenetics, Aging, and Longevity in Model Organisms

Late Passage Cultivation Induces Aged Astrocyte Phenotypes in Rat Primary Cultured Cells

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Bang, Minji, Gonzales, Edson Luck, Shin, Chan Young, Kwon, Kyoung Ja·2021·Biomolecules & Therapeutics

Abstract

aged astrocyte model through late passage cultivation of rat primary cultured astrocytes. Astrocytes were cultured until passage 7 (P7) as late passage astrocytes and compared with passage 1 (P1) astrocytes as early passage astrocytes to confirm the differences in phenotypes and the effects of serial passage. In this study, we confirmed the morphological, molecular, and functional changes of late passage astrocytes showing aging phenotypes through SA-β-gal staining and measurement of nuclear size. We also observed a reduced expression of inflammatory mediators including IL-1β, IL-6, TNFα, iNOS, and COX2, as well as dysregulation of wound-healing, phagocytosis, and mitochondrial functions such as mitochondrial membrane potential and mitochondrial oxygen consumption rate. Culture-conditioned media obtained from P1 astrocytes promoted neurite outgrowth in immature primary cultures of rat cortices, which is significantly reduced when we treated the immature neurons with the culture media obtained from P7 astrocytes. These results suggest that late passage astrocytes show senescent astrocyte phenotypes with functional defects, which makes it a suitable model for the study of the role of astrocyte senescence on the modulation of normal and pathological brain aging.

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  • After repeated subculture for 8 weeks, astrocytes almost lost their proliferative ability, manifested as over 80% of cells expressing SA-β-Gal.

    “Some astrocytes were repeatedly subcultured for 8 weeks to establish a replicated aging model. At this point, astrocytes almost lost their proliferative ability, manifested as over 80% of cells expressing SA‐β‐Gal [78, 79].”

    From Aerobic exercise improves astrocyte mitochondrial quality and transfer to neurons in a mouse model of Alzheimer's disease (2025) · cites this paper as [78]

    The Methods (Rat primary cortical astrocyte culture; page unavailable) describe repeated subculture to passage 7, and the Results (Late passage astrocytes show phenotypes of morphologically aged cells; page unavailable) report more SA-β-gal-positive cells than at passage 1. Our copy does not establish an eight-week duration, near-total loss of proliferative ability, or SA-β-gal positivity in over 80% of cells; it reports an approximately 1.3-fold increase instead. (LLM, conf=0.87)

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Research works printed but not linked: 68

  1. Abbott N. J. 2002 Astrocyte-endothelial interactions and blood-brain barrier permeability J. Anat. 200 629 638 10.1046/j.1469-7580.2002.00064.x 12162730 PMC1570746 · DOI · Paper page
  2. Acosta C. Anderson H. D. Anderson C. M. 2017 Astrocyte dysfunction in Alzheimer disease J. Neurosci. Res. 95 2430 2447 10.1002/jnr.24075 28467650 · DOI
  3. Bang M. Kim D. G. Gonzales E. L. Kwon K. J. Shin C. Y. 2019a Etoposide induces mitochondrial dysfunction and cellular senescence in primary cultured rat astrocytes Biomol. Ther. (Seoul) 27 530 539 10.4062/biomolther.2019.151 31646843 PMC6824621 · DOI
  4. Bang M. Ryu O. Kim D. G. Mabunga D. F. Cho K. S. Kim Y. Han S. H. Kwon K. J. Shin C. Y. 2019b Tenovin-1 induces senescence and decreases wound-healing activity in cultured rat primary astrocytes Biomol. Ther. (Seoul) 27 283 289 10.4062/biomolther.2018.107 30092626 PMC6513186 · DOI
  5. Bhaumik D. Scott G. K. Schokrpur S. Patil C. K. Orjalo A. V. Rodier F. Lithgow G. J. Campisi J. 2009 MicroRNAs miR-146a/b negatively modulate the senescence-associated inflammatory mediators IL-6 and IL-8 Aging (Albany N.Y.) 1 402 411 10.18632/aging.100042 20148189 PMC2818025 · DOI · Paper page
  6. Blomquist E. Westermark B. Ponten J. 1980 Ageing of human glial cells in culture: increase in the fraction of non-dividers as demonstrated by a minicloning technique Mech. Ageing Dev. 12 173 182 10.1016/0047-6374(80)90093-7 7366254 · DOI
  7. Boraschi D. Italiani P. 2014 Immunosenescence and vaccine failure in the elderly: strategies for improving response Immunol. Lett. 162 346 353 10.1016/j.imlet.2014.06.006 24960535 · DOI · Paper page
  8. Burda J. E. Bernstein A. M. Sofroniew M. V. 2016 Astrocyte roles in traumatic brain injury Exp. Neurol. 275 Pt 3 305 315 10.1016/j.expneurol.2015.03.020 25828533 PMC4586307 · DOI
  9. Caldeira C. Oliveira A. F. Cunha C. Vaz A. R. Falcao A. S. Fernandes A. Brites D. 2014 Microglia change from a reactive to an age-like phenotype with the time in culture Front. Cell. Neurosci. 8 152 10.3389/fncel.2014.00152 24917789 PMC4040822 · DOI · Paper page
  10. Campisi J. Andersen J. K. Kapahi P. Melov S. 2011 Cellular senescence: a link between cancer and age-related degenerative disease? Semin. Cancer Biol. 21 354 359 10.1016/j.semcancer.2011.09.001 21925603 PMC3230665 · DOI · Paper page
  11. Campuzano O. Castillo-Ruiz M. M. Acarin L. Castellano B. Gonzalez B. 2009 Increased levels of proinflammatory cytokines in the aged rat brain attenuate injury-induced cytokine response after excitotoxic damage J. Neurosci. Res. 87 2484 2497 10.1002/jnr.22074 19326443 · DOI
  12. Chang H. N. Pang J. H. Chen C. P. Ko P. C. Lin M. S. Tsai W. C. Yang Y. M. 2012 The effect of aging on migration, proliferation, and collagen expression of tenocytes in response to ciprofloxacin J. Orthop. Res. 30 764 768 10.1002/jor.21576 22021103 · DOI
  13. Collins-Hooper H. Woolley T. E. Dyson L. Patel A. Potter P. Baker R. E. Gaffney E. A. Maini P. K. Dash P. R. Patel K. 2012 Age-related changes in speed and mechanism of adult skeletal muscle stem cell migration Stem Cells 30 1182 1195 10.1002/stem.1088 22593017 · DOI
  14. Dai W. Zhou J. Jin B. Pan J. 2016 Class III-specific HDAC inhibitor Tenovin-6 induces apoptosis, suppresses migration and eliminates cancer stem cells in uveal melanoma Sci. Rep. 6 22622 10.1038/srep22622 26940009 PMC4778058 · DOI
  15. De Cecco M. Jeyapalan J. Zhao X. Tamamori-Adachi M. Sedivy J. M. 2011 Nuclear protein accumulation in cellular senescence and organismal aging revealed with a novel single-cell resolution fluorescence microscopy assay Aging (Albany N.Y.) 3 955 967 10.18632/aging.100372 22006542 PMC3229972 · DOI
  16. Dimri G. P. Lee X. Basile G. Acosta M. Scott G. Roskelley C. Medrano E. E. Linskens M. Rubelj I. Pereira-Smith O. 1995 A biomarker that identifies senescent human cells in culture and in aging skin in vivo Proc. Natl. Acad. Sci. U.S.A. 92 9363 9367 10.1073/pnas.92.20.9363 7568133 PMC40985 · DOI · Paper page
  17. Dossi E. Vasile F. Rouach N. 2018 Human astrocytes in the diseased brain Brain Res. Bull. 136 139 156 10.1016/j.brainresbull.2017.02.001 28212850 PMC5766741 · DOI · Paper page
  18. Eckman E. A. Reed D. K. Eckman C. B. 2001 Degradation of the Alzheimer's amyloid beta peptide by endothelin-converting enzyme J. Biol. Chem. 276 24540 24548 10.1074/jbc.M007579200 11337485 · DOI
  19. Eckman E. A. Watson M. Marlow L. Sambamurti K. Eckman C. B. 2003 Alzheimer's disease beta-amyloid peptide is increased in mice deficient in endothelin-converting enzyme J. Biol. Chem. 278 2081 2084 10.1074/jbc.C200642200 12464614 · DOI
  20. Enokido Y. Yoshitake A. Ito H. Okazawa H. 2008 Age-dependent change of HMGB1 and DNA double-strand break accumulation in mouse brain Biochem. Biophys. Res. Commun. 376 128 133 10.1016/j.bbrc.2008.08.108 18762169 · DOI
  21. Evans R. J. Wyllie F. S. Wynford-Thomas D. Kipling D. Jones C. J. 2003 A P53-dependent, telomere-independent proliferative life span barrier in human astrocytes consistent with the molecular genetics of glioma development Cancer Res. 63 4854 4861 12941806
  22. Frankel D. Mehindate K. Schipper H. M. 2000 Role of heme oxygenase-1 in the regulation of manganese superoxide dismutase gene expression in oxidatively-challenged astroglia J. Cell. Physiol. 185 80 86 10.1002/1097-4652(200010)185:1<80::AID-JCP7>3.0.CO;2-W 10942521 · DOI
  23. Gerland L. M. Peyrol S. Lallemand C. Branche R. Magaud J. P. Ffrench M. 2003 Association of increased autophagic inclusions labeled for beta-galactosidase with fibroblastic aging Exp. Gerontol. 38 887 895 10.1016/S0531-5565(03)00132-3 12915210 · DOI · Paper page
  24. Golomb L. Sagiv A. Pateras I. S. Maly A. Krizhanovsky V. Gorgoulis V. G. Oren M. Ben-Yehuda A. 2015 Age-associated inflammation connects RAS-induced senescence to stem cell dysfunction and epidermal malignancy Cell Death Differ. 22 1764 1774 10.1038/cdd.2015.21 26434982 PMC4648323 · DOI · Paper page
  25. Green S. J. Mellouk S. Hoffman S. L. Meltzer M. S. Nacy C. A. 1990 Cellular mechanisms of nonspecific immunity to intracellular infection: cytokine-induced synthesis of toxic nitrogen oxides from L-arginine by macrophages and hepatocytes Immunol. Lett. 25 15 19 10.1016/0165-2478(90)90083-3 2126524 · DOI
  26. Grolleau-Julius A. Harning E. K. Abernathy L. M. Yung R. L. 2008 Impaired dendritic cell function in aging leads to defective antitumor immunity Cancer Res. 68 6341 6349 10.1158/0008-5472.CAN-07-5769 18676859 PMC2575813 · DOI
  27. Halle A. Hornung V. Petzold G. C. Stewart C. R. Monks B. G. Reinheckel T. Fitzgerald K. A. Latz E. Moore K. J. Golenbock D. T. 2008 The NALP3 inflammasome is involved in the innate immune response to amyloid-beta Nat. Immunol. 9 857 865 10.1038/ni.1636 18604209 PMC3101478 · DOI · Paper page
  28. Hayflick L. Moorhead P. S. 1961 The serial cultivation of human diploid cell strains Exp. Cell Res. 25 585 621 10.1016/0014-4827(61)90192-6 13905658 · DOI · Paper page
  29. Hong S. H. Lee M. H. Koo M. A. Seon G. M. Park Y. J. Kim D. Park J. C. 2019 Stem cell passage affects directional migration of stem cells in electrotaxis Stem Cell Res. 38 101475 10.1016/j.scr.2019.101475 31176110 · DOI
  30. Hou J. Cui C. Kim S. Sung C. Choi C. 2018 Ginsenoside F1 suppresses astrocytic senescence-associated secretory phenotype Chem. Biol. Interact. 283 75 83 10.1016/j.cbi.2018.02.002 29412148 · DOI
  31. Hsu J. Y. Bourguignon L. Y. Adams C. M. Peyrollier K. Zhang H. Fandel T. Cun C. L. Werb Z. Noble-Haeusslein L. J. 2008 Matrix metalloproteinase-9 facilitates glial scar formation in the injured spinal cord J. Neurosci. 28 13467 13477 10.1523/JNEUROSCI.2287-08.2008 19074020 PMC2712293 · DOI
  32. Izadpanah R. Kaushal D. Kriedt C. Tsien F. Patel B. Dufour J. Bunnell B. A. 2008 Long-term in vitro expansion alters the biology of adult mesenchymal stem cells Cancer Res. 68 4229 4238 10.1158/0008-5472.CAN-07-5272 18519682 PMC2713721 · DOI
  33. Jung Y. J. Chung W. S. 2018 Phagocytic roles of glial cells in healthy and diseased brains Biomol. Ther. (Seoul) 26 350 357 10.4062/biomolther.2017.133 29316776 PMC6029679 · DOI · Paper page
  34. Lee B. Y. Han J. A. Im J. S. Morrone A. Johung K. Goodwin E. C. Kleijer W. J. DiMaio D. Hwang E. S. 2006 Senescence-associated beta-galactosidase is lysosomal beta-galactosidase Aging Cell 5 187 195 10.1111/j.1474-9726.2006.00199.x 16626397 · DOI · Paper page
  35. Li Y. N. Pan R. Qin X. J. Yang W. L. Qi Z. Liu W. Liu K. J. 2014 Ischemic neurons activate astrocytes to disrupt endothelial barrier via increasing VEGF expression J. Neurochem. 129 120 129 10.1111/jnc.12611 24251624 PMC3965617 · DOI
  36. Lian J. Lv S. Liu C. Liu Y. Wang S. Guo X. Nan F. Yu H. He X. Sun G. Ma X. 2016 Effects of serial passage on the characteristics and cardiac and neural differentiation of human umbilical cord Wharton's jelly-derived mesenchymal stem cells Stem Cells Int. 2016 9291013 10.1155/2016/9291013 26798365 PMC4699056 · DOI
  37. Logan S. Pharaoh G. A. Marlin M. C. Masser D. R. Matsuzaki S. Wronowski B. Yeganeh A. Parks E. E. Premkumar P. Farley J. A. Owen D. B. Humphries K. M. Kinter M. Freeman W. M. Szweda L. I. Van Remmen H. Sonntag W. E. 2018 Insulin-like growth factor receptor signaling regulates working memory, mitochondrial metabolism, and amyloid-beta uptake in astrocytes Mol. Metab. 9 141 155 10.1016/j.molmet.2018.01.013 29398615 PMC5870102 · DOI
  38. Lutz C. T. Quinn L. S. 2012 Sarcopenia, obesity, and natural killer cell immune senescence in aging: altered cytokine levels as a common mechanism Aging (Albany N.Y.) 4 535 546 10.18632/aging.100482 22935594 PMC3461341 · DOI
  39. McHugh D. Gil J. 2018 Senescence and aging: causes, consequences, and therapeutic avenues J. Cell Biol. 217 65 77 10.1083/jcb.201708092 29114066 PMC5748990 · DOI · Paper page
  40. Miranda C. J. Braun L. Jiang Y. Hester M. E. Zhang L. Riolo M. Wang H. Rao M. Altura R. A. Kaspar B. K. 2012 Aging brain microenvironment decreases hippocampal neurogenesis through Wnt-mediated survivin signaling Aging Cell 11 542 552 10.1111/j.1474-9726.2012.00816.x 22404871 PMC3350615 · DOI
  41. Montgomery R. R. Shaw A. C. 2015 Paradoxical changes in innate immunity in aging: recent progress and new directions J. Leukoc. Biol. 98 937 943 10.1189/jlb.5MR0315-104R 26188078 PMC4661037 · DOI · Paper page
  42. Moraga A. Pradillo J. M. Garcia-Culebras A. Palma-Tortosa S. Ballesteros I. Hernandez-Jimenez M. Moro M. A. Lizasoain I. 2015 Aging increases microglial proliferation, delays cell migration, and decreases cortical neurogenesis after focal cerebral ischemia J. Neuroinflammation 12 87 10.1186/s12974-015-0314-8 25958332 PMC4437744 · DOI
  43. Munoz-Najar U. Sedivy J. M. 2011 Epigenetic control of aging Antioxid. Redox Signal. 14 241 259 10.1089/ars.2010.3250 20518699 PMC3014766 · DOI
  44. Murphy N. Lynch M. A. 2012 Activation of the P2X(7) receptor induces migration of glial cells by inducing cathepsin B degradation of tissue inhibitor of metalloproteinase 1 J. Neurochem. 123 761 770 10.1111/jnc.12031 23017058 · DOI
  45. Nadal-Nicolas F. M. Galindo-Romero C. Valiente-Soriano F. J. Barbera-Cremades M. deTorre-Minguela C. Salinas-Navarro M. Pelegrin P. Agudo-Barriuso M. 2016 Involvement of P2X7 receptor in neuronal degeneration triggered by traumatic injury Sci. Rep. 6 38499 10.1038/srep38499 27929040 PMC5144087 · DOI
  46. Pertusa M. Garcia-Matas S. Rodriguez-Farre E. Sanfeliu C. Cristofol R. 2007 Astrocytes aged in vitro show a decreased neuroprotective capacity J. Neurochem. 101 794 805 10.1111/j.1471-4159.2006.04369.x 17250685 · DOI · Paper page
  47. Phatnani H. Maniatis T. 2015 Astrocytes in neurodegenerative disease Cold Spring Harb. Perspect. Biol. 7 a020628 10.1101/cshperspect.a020628 25877220 PMC4448607 · DOI · Paper page
  48. Poland G. A. Ovsyannikova I. G. Kennedy R. B. Lambert N. D. Kirkland J. L. 2014 A systems biology approach to the effect of aging, immunosenescence and vaccine response Curr. Opin. Immunol. 29 62 68 10.1016/j.coi.2014.04.005 24820347 PMC4119552 · DOI
  49. Ponten J. Macintyre E. H. 1968 Long term culture of normal and neoplastic human glia Acta Pathol. Microbiol. Scand. 74 465 486 10.1111/j.1699-0463.1968.tb03502.x 4313504 · DOI
  50. Ponten J. Stein W. D. Shall S. 1983 A quantitative analysis of the aging of human glial cells in culture J. Cell. Physiol. 117 342 352 10.1002/jcp.1041170309 6361044 · DOI
  51. Rosenstiel P. Derer S. Till A. Hasler R. Eberstein H. Bewig B. Nikolaus S. Nebel A. Schreiber S. 2008 Systematic expression profiling of innate immune genes defines a complex pattern of immunosenescence in peripheral and intestinal leukocytes Genes Immun. 9 103 114 10.1038/sj.gene.6364454 18216864 · DOI
  52. Rozovsky I. Wei M. Morgan T. E. Finch C. E. 2005 Reversible age impairments in neurite outgrowth by manipulations of astrocytic GFAP Neurobiol. Aging 26 705 715 10.1016/j.neurobiolaging.2004.06.009 15708446 · DOI
  53. Sadaba M. C. Martin-Estal I. Puche J. E. Castilla-Cortazar I. 2016 Insulin-like growth factor 1 (IGF-1) therapy: mitochondrial dysfunction and diseases Biochim. Biophys. Acta 1862 1267 1278 10.1016/j.bbadis.2016.03.010 27020404 · DOI
  54. Salminen A. Ojala J. Kaarniranta K. Haapasalo A. Hiltunen M. Soininen H. 2011 Astrocytes in the aging brain express characteristics of senescence-associated secretory phenotype Eur. J. Neurosci. 34 3 11 10.1111/j.1460-9568.2011.07738.x 21649759 · DOI · Paper page
  55. Schipper H. M. Bernier L. Mehindate K. Frankel D. 1999 Mitochondrial iron sequestration in dopamine-challenged astroglia: role of heme oxygenase-1 and the permeability transition pore J. Neurochem. 72 1802 1811 10.1046/j.1471-4159.1999.0721802.x 10217256 · DOI
  56. Scuderi C. Stecca C. Iacomino A. Steardo L. 2013 Role of astrocytes in major neurological disorders: the evidence and implications IUBMB Life 65 957 961 10.1002/iub.1223 24376207 · DOI
  57. Seifert G. Schilling K. Steinhauser C. 2006 Astrocyte dysfunction in neurological disorders: a molecular perspective Nat. Rev. Neurosci. 7 194 206 10.1038/nrn1870 16495941 · DOI
  58. Shall S. Stein W. D. 1979 A mortalization theory for the control of the cell proliferation and for the origin of immortal cell lines J. Theor. Biol. 76 219 231 10.1016/0022-5193(79)90371-0 431096 · DOI
  59. Sidoryk-Wegrzynowicz M. Wegrzynowicz M. Lee E. Bowman A. B. Aschner M. 2011 Role of astrocytes in brain function and disease Toxicol. Pathol. 39 115 123 10.1177/0192623310385254 21075920 PMC6218934 · DOI
  60. Simard M. Nedergaard M. 2004 The neurobiology of glia in the context of water and ion homeostasis Neuroscience 129 877 896 10.1016/j.neuroscience.2004.09.053 15561405 · DOI
  61. Sochocka M. Sobczynski M. Sender-Janeczek A. Zwolinska K. Blachowicz O. Tomczyk T. Zietek M. Leszek J. 2017 Association between periodontal health status and cognitive abilities. The role of cytokine profile and systemic inflammation Curr. Alzheimer Res. 14 978 990 10.2174/1567205014666170316163340 28317488 PMC5676025 · DOI
  62. Wagner W. Bork S. Horn P. Krunic D. Walenda T. Diehlmann A. Benes V. Blake J. Huber F. X. Eckstein V. Boukamp P. Ho A. D. 2009 Aging and replicative senescence have related effects on human stem and progenitor cells PLoS ONE 4 e5846 10.1371/journal.pone.0005846 19513108 PMC2688074 · DOI
  63. Wittko I. M. Schanzer A. Kuzmichev A. Schneider F. T. Shibuya M. Raab S. Plate K. H. 2009 VEGFR-1 regulates adult olfactory bulb neurogenesis and migration of neural progenitors in the rostral migratory stream in vivo J. Neurosci. 29 8704 8714 10.1523/JNEUROSCI.5527-08.2009 19587277 PMC3865485 · DOI
  64. Wong C. Goldstein D. R. 2013 Impact of aging on antigen presentation cell function of dendritic cells Curr. Opin. Immunol. 25 535 541 10.1016/j.coi.2013.05.016 23806201 PMC3775944 · DOI
  65. Yin K. J. Cirrito J. R. Yan P. Hu X. Xiao Q. Pan X. Bateman R. Song H. Hsu F. F. Turk J. Xu J. Hsu C. Y. Mills J. C. Holtzman D. M. Lee J. M. 2006 Matrix metalloproteinases expressed by astrocytes mediate extracellular amyloid-beta peptide catabolism J. Neurosci. 26 10939 10948 10.1523/JNEUROSCI.2085-06.2006 17065436 PMC6674654 · DOI · Paper page
  66. Yoon K. B. Park K. R. Kim S. Y. Han S. Y. 2016 Induction of nuclear enlargement and senescence by sirtuin inhibitors in glioblastoma cells Immune. Netw. 16 183 188 10.4110/in.2016.16.3.183 27340387 PMC4917402 · DOI
  67. Yu Z. Yi M. Wei T. Gao X. Chen H. 2017 KCa3.1 inhibition switches the astrocyte phenotype during astrogliosis associated with ischemic stroke via endoplasmic reticulum stress and MAPK signaling pathways Front. Cell. Neurosci. 11 319 10.3389/fncel.2017.00319 29075181 PMC5643415 · DOI
  68. Zhu L. Yu J. Shi Q. Lu W. Liu B. Xu S. Wang L. Han J. Wang X. 2011 Strain- and age-related alteration of proteins in the brain of SAMP8 and SAMR1 mice J. Alzheimers Dis. 23 641 654 10.3233/JAD-2010-101389 21178285 · DOI

Cited by

Sorted by citations

Authors
Bang, M., Gonzales, E. L., Shin, C. Y., & Kwon, K. J.
Affiliations
Konkuk University (KR)
Corresponding author
Kwon, Kyoung Ja
Venue
Biomolecules & Therapeutics
Published
2021-03-01
Volume
29
Issue
2
Pages
144-153
ISSN
  • 1976-9148 (ISSN-L)
  • 2005-4483
OpenAlex
W3109498668
Cited by
19
References
8
Citations by year
2026: 3 · 2025: 2 · 2024: 3 · 2023: 3 · 2022: 7 · 2021: 1
FWCI
1.05
Type
journal article
Language
en
Open access
Locations
  • Biomolecules & Therapeutics (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
Funders
Konkuk University
Topics
  • Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
  • Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
Keywords
astrocyte senescence, primary astrocyte culture, brain aging, senescence-associated β-galactosidase, inflammatory mediators, mitochondrial dysfunction, mitochondrial membrane potential, mitochondrial oxygen consumption, neurite outgrowth, phagocytosis, wound healing

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