IL-17 and immunologically induced senescence regulate response to injury in osteoarthritis
Open accessAbstract
Senescent cells (SnCs) are implicated in the pathogenesis of age-related diseases including osteoarthritis (OA), in part via expression of a senescence-associated secretory phenotype (SASP) that includes immunologically relevant factors and cytokines. In a model of posttraumatic OA (PTOA), anterior cruciate ligament transection (ACLT) induced a type 17 immune response in the articular compartment and draining inguinal lymph nodes (LNs) that paralleled expression of the senescence marker p16INK4a (Cdkn2a) and p21 (Cdkn1a). Innate lymphoid cells, γδ+ T cells, and CD4+ T cells contributed to IL-17 expression. Intra-articular injection of IL-17-neutralizing antibody reduced joint degeneration and decreased expression of the senescence marker Cdkn1a. Local and systemic senolysis was required to attenuate tissue damage in aged animals and was associated with decreased IL-17 and increased IL-4 expression in the articular joint and draining LNs. In vitro, we found that Th17 cells induced senescence in fibroblasts and that SnCs skewed naive T cells toward Th17 or Th1, depending on the presence of TGF-β. The SASP profile of the inflammation-induced SnCs included altered Wnt signaling, tissue remodeling, and cell-cycle pathways not previously implicated in senescence. These findings provide molecular targets and mechanisms for senescence induction and therapeutic strategies to support tissue healing in an aged environment.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In a mouse osteoarthritis model, UBX0101 combined with N was necessary to restore aged joint structure.
“in a mouse model of osteoarthritis, a combination of UBX0101 with N was necessary to restore aged joint structure131.”
From Cellular senescence and senolytics: the path to the clinic (2022) · cites this paper as [131]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
A biomarker that identifies senescent human cells in culture and in aging skin in vivo.
Dimri, G. P., Lee, X., Basile, G., Acosta, M., Scott, G., Roskelley, C., Medrano, E. E., Linskens, M., Rubelj, I., & Pereira-Smith, O. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.20.9363 · Cited by 7,477 · see citing works
The senescence-associated secretory phenotype: the dark side of tumor suppression
Coppé, J.-P., Desprez, P.-Y., Krtolica, A., & Campisi, J. (2010) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathol-121808-102144 · Cited by 5,206 · see citing works
Self-citationKorn, T., Bettelli, E., Oukka, M., & Kuchroo, V. K. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132710 · Cited by 4,873 · see citing works
Oppmann, B., Lesley, R., Blom, B., Timans, J. C., Xu, Y., Hunte, B., Vega, F., Yu, N., Wang, J., Singh, K. P., et al. (2000) · Immunity · doi:10.1016/s1074-7613(00)00070-4 · Cited by 2,819 · see citing works
Cellular senescence in aging and age-related disease: from mechanisms to therapy
Childs, B. G., Durik, M., Baker, D. J., & van Deursen, J. M. (2015) · Nature Medicine · doi:10.1038/nm.4000 · Cited by 2,363 · see citing works
An Essential Role for Senescent Cells in Optimal Wound Healing through Secretion of PDGF-AA
Demaria, M., Ohtani, N., Youssef, S. A., Rodier, F., Toussaint, W., Mitchell, J. R., Laberge, R.-M., Vijg, J., Van Steeg, H., Dollé, M. E. T., et al. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.11.012 · Cited by 2,045 · see citing works
Self-citationClearance of senescent cells by ABT263 rejuvenates aged hematopoietic stem cells in mice
Chang, J., Wang, Y., Shao, L., Laberge, R.-M., Demaria, M., Campisi, J., Janakiraman, K., Sharpless, N. E., Ding, S., Feng, W., et al. (2016) · Nature Medicine · doi:10.1038/nm.4010 · Cited by 1,819 · see citing works
Self-citationKraus, V. B., Huebner, J. L., DeGroot, J., & Bendele, A. M. (2010) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2010.04.015 · Cited by 1,773 · see citing works
Glasson, S. S., Chambers, M. G., Van Den Berg, W. B., & Little, C. B. (2010) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2010.05.025 · Cited by 1,708 · see citing works
Divergent Pro- and Antiinflammatory Roles for IL-23 and IL-12 in Joint Autoimmune Inflammation
Murphy, C. A., Langrish, C. L., Chen, Y., Blumenschein, W., McClanahan, T., Kastelein, R. A., Sedgwick, J. D., & Cua, D. J. (2003) · The Journal of Experimental Medicine · doi:10.1084/jem.20030896 · Cited by 1,669 · see citing works
Inflammation and wound healing: the role of the macrophage
Koh, T. J., & DiPietro, L. A. (2011) · Expert Reviews in Molecular Medicine · doi:10.1017/s1462399411001943 · Cited by 1,667 · see citing works
The IL-23-IL-17 immune axis: from mechanisms to therapeutic testing
Gaffen, S. L., Jain, R., Garg, A. V., & Cua, D. J. (2014) · Nature reviews. Immunology · doi:10.1038/nri3707 · Cited by 1,585 · see citing works
Jeon, O. H., Kim, C., Laberge, R.-M., Demaria, M., Rathod, S., Vasserot, A. P., Chung, J. W., Kim, D. H., Poon, Y., David, N., et al. (2017) · Nature Medicine · doi:10.1038/nm.4324 · Cited by 1,515 · cited 6× · see citing works
“We previously demonstrated that IL-1β expression increased in the joint after injury and decreased after senolytic treatment (1).”
BackgroundInfluentialSelf-citationLow-grade inflammation as a key mediator of the pathogenesis of osteoarthritis
Robinson, W., Lepus, C. M., Wang, Q., Raghu, H., Mao, R., Lindstrom, T., & Sokolove, J. (2016) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2016.136 · Cited by 1,462 · see citing works
Clearance of senescent glial cells prevents tau-dependent pathology and cognitive decline
Bussian, T. J., Aziz, A., Meyer, C. F., Swenson, B. L., van Deursen, J. M., & Baker, D. J. (2018) · Nature · doi:10.1038/s41586-018-0543-y · Cited by 1,289 · see citing works
Senescent intimal foam cells are deleterious at all stages of atherosclerosis
Childs, B. G., Baker, D. J., Wijshake, T., Conover, C. A., Campisi, J., & van Deursen, J. M. (2016) · Science · doi:10.1126/science.aaf6659 · Cited by 1,195 · see citing works
Self-citationSynovitis in osteoarthritis: current understanding with therapeutic implications
Mathiessen, A., & Conaghan, P. G. (2017) · Arthritis Research & Therapy · doi:10.1186/s13075-017-1229-9 · Cited by 1,071 · see citing works
Zhen, G., Wen, C., Jia, X., Li, Y., Crane, J. L., Mears, S. C., Askin, F. B., Frassica, F. J., Chang, W., Yao, J., et al. (2013) · Nature Medicine · doi:10.1038/nm.3143 · Cited by 946 · see citing works
Wilson, W. H., O'Connor, O. A., Czuczman, M. S., LaCasce, A. S., Gerecitano, J. F., Leonard, J. P., Tulpule, A., Dunleavy, K., Xiong, H., Chiu, Y.-L., et al. (2010) · The Lancet Oncology · doi:10.1016/s1470-2045(10)70261-8 · Cited by 876 · cited 1× · see citing works
“Thrombocytopenia had a dose-limiting effect in clinical trials, though neutropenia and a reduction in circulating lymphocytes were also observed (53), consistent with the role of these pathways in lymphocyte maturation (54).”
BackgroundType 2 Innate Signals Stimulate Fibro/Adipogenic Progenitors to Facilitate Muscle Regeneration
Heredia, J. E., Mukundan, L., Chen, F. M., Mueller, A. A., Deo, R. C., Locksley, R. M., Rando, T. A., & Chawla, A. (2013) · Cell · doi:10.1016/j.cell.2013.02.053 · Cited by 818 · see citing works
Causes, consequences, and reversal of immune system aging
Montecino-Rodriguez, E., Berent-Maoz, B., & Dorshkind, K. (2013) · Journal of Clinical Investigation · doi:10.1172/jci64096 · Cited by 793 · see citing works
How do Regulatory T Cells Work?
Corthay, A. (2009) · Scandinavian Journal of Immunology · doi:10.1111/j.1365-3083.2009.02308.x · Cited by 650 · see citing works
Robinette, M. L., Fuchs, A. G., Cortez, V. S., Lee, J. S., Wang, Y., Durum, S. K., Gilfillan, S., & Colonna, M. (2015) · Nature Immunology · doi:10.1038/ni.3094 · Cited by 644 · see citing works
Developing a pro-regenerative biomaterial scaffold microenvironment requires T helper 2 cells
Sadtler, K., Estrellas, K., Allen, B. W., Wolf, M. T., Fan, H., Tam, A. J., Patel, C. H., Luber, B. S., Wang, H., Wagner, K. R., et al. (2016) · Science · doi:10.1126/science.aad9272 · Cited by 605 · see citing works
Self-citationImpaired immune surveillance accelerates accumulation of senescent cells and aging
Ovadya, Y., Landsberger, T., Leins, H., Vadai, E., Gal, H., Biran, A., Yosef, R., Sagiv, A., Agrawal, A., Shapira, A., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07825-3 · Cited by 578 · see citing works
Biernacka, A., & Frangogiannis, N. G. (2011) · Europe PMC (PubMed Central) · Cited by 456 · see citing works
The IL-23-IL-17 axis in inflammatory arthritis
Lubberts, E. (2015) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2015.53 · Cited by 442 · see citing works
The central role of muscle stem cells in regenerative failure with aging
Blau, H. M., Cosgrove, B. D., & Ho, A. T. V. (2015) · Nature Medicine · doi:10.1038/nm.3918 · Cited by 437 · see citing works
Source of chronic inflammation in aging
Sanada, F., Taniyama, Y., Muratsu, J., Otsu, R., Shimizu, H., Rakugi, H., & Morishita, R. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00012 · Cited by 413 · see citing works
Yang, Y., Topol, L. Z., Lee, H., & Wu, J. (2003) · Development · doi:10.1242/dev.00324 · Cited by 398 · see citing works
Regulation of Lymphocyte Survival by the BCL-2 Gene Family
Cory, S. (1995) · Annual Review of Immunology · doi:10.1146/annurev.iy.13.040195.002501 · Cited by 385 · see citing works
Bone development and age-related bone loss in male C57BL/6J mice
Ferguson, V. L., Ayers, R. A., Bateman, T. A., & Simske, S. J. (2003) · Bone · doi:10.1016/s8756-3282(03)00199-6 · Cited by 379 · see citing works
Mi, S., Li, Z., Yang, H.-Z., Liu, H., Wang, J.-P., Ma, Y.-G., Wang, X.-X., Liu, H.-Z., Sun, W., & Hu, Z.-W. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1004081 · Cited by 370 · see citing works
Inflammaging decreases adaptive and innate immune responses in mice and humans
Frasca, D., & Blomberg, B. B. (2016) · Biogerontology · doi:10.1007/s10522-015-9578-8 · Cited by 357 · see citing works
Senescent cells and osteoarthritis: a painful connection
Jeon, O. H., David, N. E., Campisi, J., & Elisseeff, J. H. (2018) · Journal of Clinical Investigation · doi:10.1172/jci95147 · Cited by 354 · see citing works
Self-citationTransplanted Senescent Cells Induce an Osteoarthritis-Like Condition in Mice
Xu, M., Bradley, E. W., Weivoda, M. M., Hwang, S. M., Pirtskhalava, T., Decklever, T., Curran, G. L., Ogrodnik, M., Jurk, D., Johnson, K. O., et al. (2016) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glw154 · Cited by 352 · see citing works
Terminally Differentiated CD8 + T Cells Negatively Affect Bone Regeneration in Humans
Reinke, S., Geißler, S., Taylor, W. R., Schmidt‐Bleek, K., Juelke, K., Schwachmeyer, V., Dahne, M., Hartwig, T., Akyüz, L., Meisel, C., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3004754 · Cited by 336 · see citing works
CCR2 chemokine receptor signaling mediates pain in experimental osteoarthritis
Miller, R. E., Tran, P. B., Das, R., Ghoreishi-Haack, N. S., Ren, D., Miller, R. J., & Malfait, A. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1209294110 · Cited by 279 · see citing works
Cell Senescence: Role in Aging and Age-Related Diseases
Campisi, J., & Robert, L. (2014) · Interdisciplinary Topics in Gerontology and Geriatrics · doi:10.1159/000358899 · Cited by 240 · see citing works
Self-citationThe role of inflammation in age-related disease
Howcroft, T. K., Campisi, J., Louis, G. B., Smith, M. T., Wise, B., Wyss-Coray, T., Augustine, A. D., McElhaney, J. E., Kohanski, R., & Sierra, F. (2013) · Aging · doi:10.18632/aging.100531 · Cited by 239 · see citing works
Self-citationThe Th17/Treg balance is disturbed during aging
Schmitt, V., Rink, L., & Uciechowski, P. (2013) · Experimental Gerontology · doi:10.1016/j.exger.2013.09.003 · Cited by 235 · see citing works
Regulation of interleukin‐12/interleukin‐23 production and the T‐helper 17 response in humans
Lyakh, L. A., Trinchieri, G., Provezza, L., Carra, G., & Gerosa, F. (2008) · Immunological Reviews · doi:10.1111/j.1600-065x.2008.00700.x · Cited by 230 · see citing works
Mouse models of osteoarthritis: modelling risk factors and assessing outcomes
Fang, H., & Beier, F. (2014) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2014.46 · Cited by 212 · see citing works
Age-related changes in immune function: Effect on airway inflammation
Busse, P. J., & Mathur, S. K. (2010) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2010.08.011 · Cited by 209 · see citing works
Making Mouse Models That Reflect Human Immune Responses
Tao, L., & Reese, T. A. (2017) · Trends in Immunology · doi:10.1016/j.it.2016.12.007 · Cited by 209 · see citing works
Proteoglycan 4 Expression Protects Against the Development of Osteoarthritis
Ruan, M. Z. C., Erez, A., Guse, K., Dawson, B., Bertin, T., Chen, Y., Jiang, M.-M., Yustein, J., Gannon, F., & Lee, B. H. L. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3005409 · Cited by 196 · see citing works
IL ‐23: One cytokine in control of autoimmunity
Croxford, A. L., Mair, F., & Becher, B. (2012) · European Journal of Immunology · doi:10.1002/eji.201242598 · Cited by 194 · see citing works
Mease, P. J. (2015) · Current Opinion in Rheumatology · doi:10.1097/bor.0000000000000147 · Cited by 171 · see citing works
Fibroblast senescence in the pathology of idiopathic pulmonary fibrosis
Waters, D. W., Blokland, K. E. C., Pathinayake, P. S., Burgess, J. K., Mutsaers, S. E., Prêle, C. M., Schuliga, M. J., Grainge, C., & Knight, D. A. (2018) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00037.2018 · Cited by 167 · see citing works
Cai, J., Weiss, M. L., & Rao, M. S. (2004) · Experimental Hematology · doi:10.1016/j.exphem.2004.03.013 · Cited by 166 · see citing works
Diekman, B. O., Sessions, G. A., Collins, J. A., Knecht, A. K., Strum, S. L., Mitin, N. K., Carlson, C. S., Loeser, R. F., & Sharpless, N. E. (2018) · Aging Cell · doi:10.1111/acel.12771 · Cited by 158 · see citing works
Cellular senescence impact on immune cell fate and function
Vicente, R., Mausset-Bonnefont, A.-L., Jorgensen, C., Louis-Plence, P., & Brondello, J.-M. (2016) · Aging Cell · doi:10.1111/acel.12455 · Cited by 151 · see citing works
Ishii, H., Tanaka, H., Katoh, K., Nakamura, H., NAGASHIMA, M., & Yoshino, S. (2002) · Osteoarthritis and Cartilage · doi:10.1053/joca.2001.0509 · Cited by 147 · see citing works
IL-17A mediates inflammatory and tissue remodelling events in early human tendinopathy
Millar, N. L., Akbar, M., Campbell, A. L., Reilly, J. H., Kerr, S. C., McLean, M., Frleta‐Gilchrist, M., Fazzi, U. G., Leach, W. J., Rooney, B. P., et al. (2016) · Scientific Reports · doi:10.1038/srep27149 · Cited by 136 · see citing works
LIF signaling in stem cells and development
Onishi, K., & Zandstra, P. W. (2015) · Development · doi:10.1242/dev.117598 · Cited by 116 · see citing works
LIF in the regulation of T-cell fate and as a potential therapeutic
Metcalfe, S. M. (2011) · Genes and Immunity · doi:10.1038/gene.2011.9 · Cited by 115 · see citing works
Liu, Y., Zhu, H., Su, Z., Sun, C., Yin, J., Yuan, H., Sandoghchian, S., Jiao, Z., Wang, S., & Xu, H. (2012) · International Immunology · doi:10.1093/intimm/dxs056 · Cited by 110 · see citing works
Osteoarthritis: can anti-cytokine therapy play a role in treatment?
Calich, A. L., Domiciano, D. S., & Fuller, R. (2010) · Clinical Rheumatology · doi:10.1007/s10067-009-1352-3 · Cited by 108 · see citing works
Pain, motor and gait assessment of murine osteoarthritis in a cruciate ligament transection model
Ruan, M. Z. C., Patel, R. M., Dawson, B., Jiang, M., & Lee, B. (2013) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2013.06.016 · Cited by 102 · see citing works
Erratum: The IL-23–IL-17 axis in inflammatory arthritis
Lubberts, E. (2015) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2015.128 · Cited by 96 · see citing works
Role of Interleukin-1 Inhibitors in Osteoarthritis
Jotanović, Z., Mihelić, R., Šestan, B., & Dembić, Z. (2012) · Drugs & Aging · doi:10.2165/11599350-000000000-00000 · Cited by 91 · see citing works
Role of the IL-23/IL-17 axis in Crohn's disease.
Siakavellas, S. I., & Bamias, G. (2012) · PubMed · Cited by 82 · see citing works
Chen, B., Deng, Y. L., Tan, Y., Qin, J., & Chen, L. (2013) · Journal of International Medical Research · doi:10.1177/0300060513501751 · Cited by 80 · see citing works
Role of IL-17 in the pathogenesis of psoriatic arthritis and axial spondyloarthritis
Raychaudhuri, S. K., Saxena, A., & Raychaudhuri, S. P. (2015) · Clinical Rheumatology · doi:10.1007/s10067-015-2961-7 · Cited by 78 · see citing works
Mechanistic rationales for targeting interleukin-17A in spondyloarthritis
Raychaudhuri, S. P., & Raychaudhuri, S. K. (2017) · Arthritis Research & Therapy · doi:10.1186/s13075-017-1249-5 · Cited by 71 · see citing works
Askari, A., Naghizadeh, M., Homayounfar, R., Shahi, A., Afsarian, M. H., Paknahad, A., Kennedy, D., & Ataollahi, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164757 · Cited by 69 · see citing works
Sohn, J. J., Schetter, A. J., Yfantis, H. G., Ridnour, L. A., Horikawa, I., Ma, K., Robles, A. I., Hussain, S. P., Goto, A., Bowman, E. D., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044156 · Cited by 66 · see citing works
Interactions between Innate Lymphoid Cells and Cells of the Innate and Adaptive Immune System
Symowski, C., & Voehringer, D. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01422 · Cited by 54 · see citing works
Systemic inflammation and painful joint burden in osteoarthritis: a matter of sex?
Perruccio, A., Chandran, V., Power, J., Kapoor, M., Mahomed, N., & Gandhi, R. (2015) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2016.08.001 · Cited by 53 · see citing works
Binks, D., Gravallese, E. M., Bergin, D., Hodgson, R. J., Tan, A. L., Matzelle, M. M., McGonagle, D. G., & Radjenovic, A. (2013) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2013-203972 · Cited by 47 · see citing works
Secukinumab for ankylosing spondylitis and psoriatic arthritis
Lubrano, E., & Perrotta, F. M. (2016) · Therapeutics and Clinical Risk Management · doi:10.2147/tcrm.s100091 · Cited by 44 · see citing works
IL-23/IL-17 axis in spondyloarthritis-bench to bedside
Raychaudhuri, S. P., & Raychaudhuri, S. K. (2016) · Clinical Rheumatology · doi:10.1007/s10067-016-3263-4 · Cited by 43 · see citing works
Innate Lymphoid Cells (ILCs) as Mediators of Inflammation, Release of Cytokines and Lytic Molecules
Elemam, N. M., Hannawi, S., & Maghazachi, A. A. (2017) · Toxins · doi:10.3390/toxins9120398 · Cited by 41 · see citing works
Defining the functional states of Th17 cells
Lee, Y., & Kuchroo, V. K. (2015) · F1000Research · doi:10.12688/f1000research.6116.1 · Cited by 31 · see citing works
Lurati, A., Laria, A., Gatti, A., Brando, B., & Scarpellini, M. (2015) · Open Access Rheumatology Research and Reviews · doi:10.2147/oarrr.s81905 · Cited by 23 · see citing works
Diekman, B. O., Thakore, P. I., O’Connor, S. K., Willard, V. P., Brunger, J. M., Christoforou, N., Leong, K. W., Gersbach, C. A., & Guilak, F. (2014) · Tissue Engineering Part A · doi:10.1089/ten.tea.2014.0240 · Cited by 18 · see citing works
Who regulates whom: ZNF341 is an additional player in the STAT3/T H 17 song
August, A. (2018) · Science Immunology · doi:10.1126/sciimmunol.aat9779 · Cited by 9 · see citing works
The Puzzle of Generalized Osteoarthritis (OA) — Is OA a Systemic Enthesopathy?
Haugen, I. K. (2012) · The Journal of Rheumatology · doi:10.3899/jrheum.111151 · Cited by 3 · see citing works
Flagged first, then by citations
2 of the 80 references couldn’t be matched to a known paper.
Research works printed but not linked: 5
- [15]15. Jeon OH, David N, Campisi J, Elisseeff JH. Senes- cent cells and osteoarthritis: a painful connec- tion. J Clin Invest. 2018;128(4):1229-1237.
- [24]24. Cai J, Weiss ML, Rao MS. In search of "stem- ness". Exp Hematol. 2004;32(7):585-598.
- [36]36. Yang Y, Topol L, Lee H, Wu J. Wnt5a and Wnt5b exhibit distinct activities in coordinating chon- drocyte proliferation and differentiation. Devel- opment. 2003;130(5):1003-1015.
- [47]47. Biernacka A, Frangogiannis NG. Aging and cardi- ac fibrosis. Aging Dis. 2011;2(2):158-173.
- [70]70. Diekman BO, et al. Expression of p16 INK4a is a bio- marker of chondrocyte aging but does not cause osteoarthritis. Aging Cell. 2018;17(4):e12771.
Cited by
Sorted by citations
Cellular senescence and senolytics: the path to the clinic
Chaib, S., Tchkonia, T., & Kirkland, J. L. (2022) · Nature Medicine · doi:10.1038/s41591-022-01923-y · Cited by 1,105 · see citing works
The senescence-associated secretory phenotype and its physiological and pathological implications
Wang, B., Han, J., Elisseeff, J. H., & Demaria, M. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-024-00727-x · Cited by 948 · see citing works
Self-citationDisease-modifying therapeutic strategies in osteoarthritis: current status and future directions
Cho, Y., Jeong, S., Kim, H., Kang, D., Lee, J., Kang, S., & Kim, J. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00710-y · Cited by 307 · see citing works
Fundamentals of osteoarthritis: Inflammatory mediators in osteoarthritis
Roover, A. D., Escribano-Núñez, A., Monteagudo, S., & Lories, R. J. U. (2023) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2023.06.005 · Cited by 288 · see citing works
Osteoarthritis year in review 2021: biology
Jiang, Y. (2021) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2021.11.009 · Cited by 268 · see citing works
The role of T cells in age-related diseases
Carrasco, E., Heras, M. M. G. D. L., Gabandé‐Rodríguez, E., Desdín-Micó, G., Aranda, J. F., & Mittelbrunn, M. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00557-4 · Cited by 244 · see citing works
Senescence in osteoarthritis: from mechanism to potential treatment
Liu, Y., Zhang, Z., Li, T., Xu, H., & Zhang, H. (2022) · Arthritis Research & Therapy · doi:10.1186/s13075-022-02859-x · Cited by 206 · see citing works
Self-citationCellular senescence in knee osteoarthritis: molecular mechanisms and therapeutic implications
Xie, J., Wang, Y., Lu, L., Liu, L., Yu, X., & Pei, F. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101413 · Cited by 174 · see citing works
Cellular senescence in musculoskeletal homeostasis, diseases, and regeneration
Wan, M., Gray-Gaillard, E. F., & Elisseeff, J. H. (2021) · Bone Research · doi:10.1038/s41413-021-00164-y · Cited by 150 · see citing works
Self-citationSirt6 attenuates chondrocyte senescence and osteoarthritis progression
Ji, M.-L., Jiang, H., Li, Z., Geng, R., Hu, J. Z., Lin, Y. C., & Lu, J. (2022) · Nature Communications · doi:10.1038/s41467-022-35424-w · Cited by 144 · see citing works
Mi, B.-B., Xiong, Y., Knoedler, S. A., Alfertshofer, M. G., Panayi, A. C., Wang, H., Lin, S.-E., Li, G., & Liu, G. (2024) · Bone Research · doi:10.1038/s41413-024-00346-4 · Cited by 138 · see citing works
Aging and the emerging role of cellular senescence in osteoarthritis
Diekman, B. O., & Loeser, R. F. (2023) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2023.11.018 · Cited by 130 · see citing works
Engineering the IL ‐4/ IL ‐13 axis for targeted immune modulation
Bernstein, Z. J., Shenoy, A., Chen, A. Y.-C., Heller, N. M., & Spangler, J. B. (2023) · Immunological Reviews · doi:10.1111/imr.13230 · Cited by 124 · see citing works
The immune system in cardiovascular diseases: from basic mechanisms to therapeutic implications
Wang, X., Chen, L., Wei, J., Zheng, H., Zhou, N., Xu, X., Deng, X., Liu, T., & Zou, Y. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02220-z · Cited by 120 · see citing works
Role of cellular senescence in inflammation and regeneration
Saito, Y., Yamamoto, S., & Chikenji, T. (2024) · Inflammation and Regeneration · doi:10.1186/s41232-024-00342-5 · Cited by 117 · see citing works
Shanley, L. C., Mahon, O. R., Kelly, D. J., & Dunne, A. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.02.023 · Cited by 108 · see citing works
Dolgin, E. (2020) · Nature Biotechnology · doi:10.1038/s41587-020-00750-1 · Cited by 95 · see citing works
Cellular senescence in skeletal disease: mechanisms and treatment
He, X., Hu, W., Zhang, Y., Chen, M., Ding, Y., Yang, H., He, F., Gu, Q., & Shi, Q. (2023) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-023-00501-5 · Cited by 96 · see citing works
Khella, C. M., Asgarian, R., Horvath, J. M., Rolauffs, B., & Hart, M. L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041996 · Cited by 91 · see citing works
Zhu, X., Huang, J.-Y., Dong, W., Tang, H.-D., Xu, S., Wu, Q., Zhang, H., Cheng, P., Jin, Y., Zhu, M., et al. (2024) · Nature Neuroscience · doi:10.1038/s41593-023-01561-8 · Cited by 85 · see citing works
Self-citationvan den Bosch, M. H. J., Blom, A. B., & van der Kraan, P. M. (2023) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2023.12.005 · Cited by 86 · see citing works
Cellular senescence and the host immune system in aging and age-related disorders
Giannoula, Y., Kroemer, G., & Pietrocola, F. (2023) · Biomedical Journal · doi:10.1016/j.bj.2023.02.001 · Cited by 81 · see citing works
State of the Art: The Immunomodulatory Role of MSCs for Osteoarthritis
Kwon, D., Kim, M., Jeon, Y., Nam, Y., Park, J. S., & Ryu, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031618 · Cited by 79 · see citing works
Osteoarthritis pathophysiology – therapeutic target discovery may require a multi-faceted approach
Vincent, T., Alliston, T., Kapoor, M., Loeser, R., Troeberg, L., & Little, C. (2022) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2021.11.015 · Cited by 73 · see citing works
A coalition to heal—the impact of the cardiac microenvironment
Tzahor, E., & Dimmeler, S. (2022) · Science · doi:10.1126/science.abm4443 · Cited by 66 · see citing works
Wu, C., Liu, R., Huan, S., Tang, W., Zeng, Y.-K., Zhang, J., Yang, J., Li, Z., Zhou, Y., Zha, Z., et al. (2022) · Arthritis Research & Therapy · doi:10.1186/s13075-022-02747-4 · Cited by 68 · see citing works
Self-citationFang, C., Liu, B., & Wan, M. (2023) · Calcified Tissue International · doi:10.1007/s00223-023-01100-4 · Cited by 69 · see citing works
Cherry, C., Andorko, J. I., Krishnan, K., Mejías, J. C., Nguyen, H. H., Stivers, K. B., Gray-Gaillard, E. F., Ruta, A., Han, J., Hamada, N., et al. (2023) · GeroScience · doi:10.1007/s11357-023-00785-7 · Cited by 66 · see citing works
Self-citationImpact of aging on treatment considerations for multiple sclerosis patients
Macaron, G., Larochelle, C., Arbour, N., Galmard, M., Girard, M., Prat, A., & Duquette, P. (2023) · Frontiers in Neurology · doi:10.3389/fneur.2023.1197212 · Cited by 67 · see citing works
Huang, Z., Luo, Z., Cai, Y. R., Chou, C.-H., Yao, M. L., Pei, F., Kraus, V. B., & Zhou, Z. (2021) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2021.12.007 · Cited by 63 · see citing works
The role of Th/Treg immune cells in osteoarthritis
Wen, Z. H., Qiu, L., Ye, Z., Tan, X., Xu, X., Lu, M., & Kuang, G. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1393418 · Cited by 63 · see citing works
Targeting Cellular Senescence for Healthy Aging: Advances in Senolytics and Senomorphics
Alum, E. U., Izah, S. C., Uti, D. E., Ugwu, O. P.-C., Betiang, P. A., Basajja, M., & Ejemot-Nwadiaro, R. I. (2025) · Drug Design Development and Therapy · doi:10.2147/dddt.s543211 · Cited by 59 · see citing works
Osteoclasts and osteoarthritis: Novel intervention targets and therapeutic potentials during aging
Wang, H., Yuan, T., Wang, Y., Liu, C., Li, D., Li, Z., & Sun, S. (2024) · Aging Cell · doi:10.1111/acel.14092 · Cited by 60 · see citing works
Khella, C. M., Horvath, J. M., Asgarian, R., Rolauffs, B., & Hart, M. L. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158005 · Cited by 54 · see citing works
Role of synovial lymphatic function in osteoarthritis
Cao, M., Ong, M. T., Yung, P. S., Tuan, R. S., & Jiang, Y. (2022) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2022.04.003 · Cited by 54 · see citing works
Dhanabalan, K. M., Dravid, A. A., Agarwal, S., Sharath, R. K., Padmanabhan, A. K., & Agarwal, R. (2022) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10298 · Cited by 53 · see citing works
Targeting cellular senescence as a novel treatment for osteoarthritis
Astrike‐Davis, E. M., Coryell, P., & Loeser, R. F. (2022) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2022.102213 · Cited by 51 · see citing works
Jiang, N., Xing, B., Peng, R., Shang, J., Wu, B., Xiao, P., Lin, S., Xu, X., & Lu, H. (2022) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2022.111688 · Cited by 51 · see citing works
Chin, A. F., Han, J., Clement, C. C., Choi, Y., Zhang, H., Browne, M., Jeon, O. H., & Elisseeff, J. H. (2023) · Aging Cell · doi:10.1111/acel.13979 · Cited by 49 · see citing works
Self-citationDing, C., Min, J., Tan, Y., Zheng, L., Ma, R., Zhao, R., Zhao, H., Ding, Q., Chen, H., & Huo, D. (2024) · Advanced Materials · doi:10.1002/adma.202401361 · Cited by 48 · see citing works
Zupan, J., Stražar, K., Kocijan, R., Nau, T., Grillari, J., & Marolt, D. (2021) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2021.111539 · Cited by 49 · see citing works
Rizzo, M. G., Best, T. M., Huard, J., Philippon, M. J., Hornicek, F. J., Duan, Z., Griswold, A. J., Kaplan, L. D., Hare, J. M., & Kouroupis, D. (2023) · Cells · doi:10.3390/cells12101421 · Cited by 46 · see citing works
Hu, K., Song, M. K., Song, T., Jia, X. H., & Song, Y.-J. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s514002 · Cited by 44 · see citing works
Okamoto, K., & Takayanagi, H. (2023) · Bone · doi:10.1016/j.bone.2023.116675 · Cited by 42 · see citing works
Gil, T., Zheng, H., Lee, H. G., Shin, J.-W., Hwang, S. W., Jang, K.-M., & Jeon, O. H. (2022) · Aging · doi:10.18632/aging.204204 · Cited by 42 · see citing works
Self-citationIL-17 in osteoarthritis: A narrative review
Xiao, J., Zhang, P., Cai, F., Luo, C.-G., Pu, T., Pan, X.-L., & Tian, M. (2023) · Open Life Sciences · doi:10.1515/biol-2022-0747 · Cited by 55 · see citing works
Wang, X., Li, X., Zhou, J., Lei, Z., & Yang, X. (2024) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2024.110890 · Cited by 40 · see citing works
Tang, S., Cao, Y., Cai, Z.-P., Nie, X., Ruan, J., Zhou, Z., Ruan, G., Zhu, Z.-H., Han, W., & Ding, C. (2022) · Science Signaling · doi:10.1126/scisignal.abm6265 · Cited by 40 · see citing works
Xu, J., Lin, S., Chen, H., Yang, G., Zhou, M., Liu, Y., Li, A., Yin, S., & Jiang, X. (2024) · Advanced Healthcare Materials · doi:10.1002/adhm.202304315 · Cited by 39 · see citing works
Periodontal disease as a model to study chronic inflammation in aging
Bertolini, M., & Clark, D. R. (2023) · GeroScience · doi:10.1007/s11357-023-00835-0 · Cited by 37 · see citing works
The impact of ageing mechanisms on musculoskeletal system diseases in the elderly
Cai, Y., Han, Z., Cheng, H., Li, H., Wang, K., Chen, J., Liu, Z., Xie, Y., Lin, Y., Zhou, S., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1405621 · Cited by 47 · see citing works
Crosstalk between bone and the immune system
Okamoto, K. (2024) · Journal of Bone and Mineral Metabolism · doi:10.1007/s00774-024-01539-x · Cited by 37 · see citing works
IL-23R is a senescence-linked circulating and tissue biomarker of aging
Carver, C. M., Rodriguez, S. L., Atkinson, E. J., Dosch, A. J., Asmussen, N. C., Gomez, P. T., Leitschuh, E. A., Espíndola‐Netto, J. M., Jeganathan, K. B., Whaley, M. G., et al. (2024) · Nature Aging · doi:10.1038/s43587-024-00752-7 · Cited by 37 · see citing works
Immunotherapies in chronic pain through modulation of neuroimmune interactions
Zhao, J., Huh, Y., Bortsov, A. V., Diatchenko, L. B., & Ji, R. (2023) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2023.108476 · Cited by 39 · see citing works
Jenei-Lanzl, Z., Maurer, S., Brenner, R. E., Zaucke, F., Fuchs, M., & Riegger, J. (2025) · Archives of pharmacal research · doi:10.1007/s12272-025-01551-3 · Cited by 35 · see citing works
Mechanism of immune infiltration in synovial tissue of osteoarthritis: a gene expression-based study
Zhang, Q., Sun, C., Liu, X., Zhu, C., Ma, C., & Feng, R. (2023) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-023-03541-x · Cited by 34 · see citing works
Immunoengineering Biomaterials for Musculoskeletal Tissue Repair across Lifespan
Han, J., Rindone, A. N., & Elisseeff, J. H. (2024) · Advanced Materials · doi:10.1002/adma.202311646 · Cited by 34 · see citing works
Self-citationTang, R., Harasymowicz, N. S., Wu, C., Choi, Y., Lenz, K. L., Oswald, S. J., & Guilak, F. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2402954121 · Cited by 34 · see citing works
Immune cell profiles in synovial fluid after anterior cruciate ligament and meniscus injuries
Kim-Wang, S. Y., Holt, A. G., McGowan, A. M., Danyluk, S. T., Goode, A. P., Lau, B. C., Toth, A. P., Wittstein, J. R., DeFrate, L. E., Yi, J. S., et al. (2021) · Arthritis Research & Therapy · doi:10.1186/s13075-021-02661-1 · Cited by 34 · see citing works
Kouri, V., Olkkonen, J., Nurmi, K., Peled, N., Ainola, M., Mandelin, J., Nordström, D., & Eklund, K. K. (2022) · Lara D. Veeken · doi:10.1093/rheumatology/keac385 · Cited by 33 · see citing works
Pathological progression of osteoarthritis: a perspective on subchondral bone
Li, X., Chen, W., Liu, D., Chen, P., Wang, S., Li, F., Chen, Q., Lv, S., Li, F., Chen, C., et al. (2024) · Frontiers of Medicine · doi:10.1007/s11684-024-1061-y · Cited by 34 · see citing works
Feng, Y., Zhang, X., Li, J., Fu, S., Xu, W., Liu, J., Yang, Y., Chen, T., Zhao, Y., Li, D., et al. (2024) · Theranostics · doi:10.7150/thno.103746 · Cited by 35 · see citing works
Oxidative Stress, Inflammation, and Cellular Senescence in Neuropathic Pain: Mechanistic Crosstalk
Stojanović, B., Bevc, I. M., Stojanovic, M. D., Stojanović, B., Lazarević, T., Spasić, M., Petrovic, M., Stefanovic, I., Marković, M., Nešić, J., et al. (2025) · Antioxidants · doi:10.3390/antiox14101166 · Cited by 33 · see citing works
Song, X., Xiao, J., Ai, X., Li, Y., Sun, L., & Chen, L. (2024) · Acta Biomaterialia · doi:10.1016/j.actbio.2024.09.034 · Cited by 31 · see citing works
Rentschler, M., Braumüller, H., Briquez, P. S., & Wieder, T. (2022) · Cancers · doi:10.3390/cancers14061364 · Cited by 31 · see citing works
T cell control of inflammaging
Shchukina, I., Boháčová, P., & Artyomov, M. N. (2023) · Seminars in Immunology · doi:10.1016/j.smim.2023.101818 · Cited by 31 · see citing works
Cellular senescence is a key mediator of lung aging and susceptibility to infection
Torrance, B. L., & Haynes, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1006710 · Cited by 28 · see citing works
Can Exercise Mend Aged-Tissue Crosstalk in Bone, to Lessen Osteoporosis & Osteoarthritis?
Little-Letsinger, S. E., Rubin, J., Diekman, B., Rubin, C., McGrath, C., Pagnotti, G., Klett, E., & Styner, M. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.08.011 · Cited by 27 · see citing works
The ageing immune system as a driver of systemic ageing
Jang, I. H., Niedernhofer, L. J., Robbins, P. D., & Camell, C. D. (2026) · Nature reviews. Immunology · doi:10.1038/s41577-026-01269-3 · Cited by 33 · see citing works
Ling, Y., Yu, X., Liu, M., & Cao, Y. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1149686 · Cited by 28 · see citing works
From the divergence of senescent cell fates to mechanisms and selectivity of senolytic drugs
L’Hôte, V., Mann, C., & Thuret, J. (2022) · Open Biology · doi:10.1098/rsob.220171 · Cited by 26 · see citing works
Neural and immune roles in osteoarthritis pain: Mechanisms and intervention strategies
Zou, Y., Liu, C., Wang, Z., Li, G., & Xiao, J. (2024) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2024.07.010 · Cited by 26 · see citing works
Shang, J., Lin, N., Peng, R., Jiang, N., Wu, B., Xing, B., Lin, S., Xu, X., & Lu, H. (2023) · Molecules · doi:10.3390/molecules28030924 · Cited by 26 · see citing works
Aging microenvironment in osteoarthritis focusing on early-stage alterations and targeted therapies
Dang, Y., Liu, Y., Zhang, B., & Zhang, X. (2025) · Bone Research · doi:10.1038/s41413-025-00465-6 · Cited by 27 · see citing works
Chen, G., Liu, X., Chen, J., Yu, X., Luo, J., Yan, Z.-R., & Tao, Q. (2021) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2021/5233462 · Cited by 25 · see citing works
ATOH8 binds SMAD3 to induce cellular senescence and prevent Ras-driven malignant transformation
Liu, X., Li, X., Wang, S., Liu, Q., Feng, X., Wang, W., Huang, Z., Huang, Y., Wu, J., Cai, M., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2208927120 · Cited by 25 · see citing works
Microenvironment-Responsive Nanosystems for Osteoarthritis Therapy
Li, S., Xiong, Y., Zhu, H., Ma, T., Sun, X., & Xiao, J. (2023) · Engineered Regeneration · doi:10.1016/j.engreg.2023.12.002 · Cited by 27 · see citing works
Feng, K., Liu, J., Gong, L., Ye, T., Chen, Z., Wang, Y., Li, Q., & Xie, X. (2025) · Advanced Science · doi:10.1002/advs.202413759 · Cited by 24 · see citing works
Synovial mast cells and osteoarthritis: Current understandings and future perspectives
Hao, G., Han, S., Xiao, Z., Shen, J., Zhao, Y., & Qi, H. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e41003 · Cited by 23 · see citing works
Immunosenescence in autoimmune diseases
Hu, H., Zhang, G., Chen, T., Liu, Y., Meng, L., Holmdahl, R., Dai, L., & Zhao, Y. C. (2025) · Autoimmunity Reviews · doi:10.1016/j.autrev.2025.103805 · Cited by 25 · see citing works
Interleukin-17A: Potential mediator and therapeutic target in hypertension
Rodrigues-Díez, R. R., Tejera‐Muñoz, A., Orejudo, M., Márquez‐Expósito, L., Santos‐Sanchez, L., Rayego‐Mateos, S., Cantero‐Navarro, E., Tejedor-Santamaria, L., Marchant, V. A., Ortíz, A., et al. (2021) · Nefrología (English Edition) · doi:10.1016/j.nefroe.2021.06.003 · Cited by 22 · see citing works
Fu, L., Duan, H., Cai, Y., Chen, X., Zou, B., Yuan, L., & Liu, G. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.116031 · Cited by 22 · see citing works
Apremilast prevents IL‑17‑induced cellular senescence in ATDC5 chondrocytes mediated by SIRT1
Wang, B., Sun, W., Bi, K., Li, Y., & Li, F. (2021) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2021.4845 · Cited by 22 · see citing works
Antisenescence Therapy Improves Function in a Human Model of Cardiac Fibrosis-on-a-Chip
Mourad, O., Mastikhina, O., Khan, S. T., Sun, X., Hatkar, R., Williams, K., & Nunes, S. S. (2023) · ACS Materials Au · doi:10.1021/acsmaterialsau.3c00009 · Cited by 21 · see citing works
Harasymowicz, N. S., Harissa, Z., Rashidi, N., Lenz, K. L., Tang, R., & Guilak, F. (2025) · Annals of the Rheumatic Diseases · doi:10.1016/j.ard.2025.03.001 · Cited by 21 · see citing works
Feng, M., Liu, W., Ding, J., Qiu, Y., & Chen, Q. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.716610 · Cited by 20 · see citing works
The Role of Senescence-Associated Secretory Phenotype in Bone Loss
Zhu, R., Wan, H.-Y., Yang, H., Song, M., Chai, Y., & Yu, B. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.841612 · Cited by 20 · see citing works
Identification of SCRG1 as a Potential Therapeutic Target for Human Synovial Inflammation
Liu, G., He, G., Zhang, J., Zhang, Z., & Wang, L. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.893301 · Cited by 20 · see citing works
Emerging therapeutic targets for osteoarthritis
Hadzic, E., & Beier, F. (2023) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2023.2185133 · Cited by 20 · see citing works
Cystathionine-γ-lyase attenuates inflammatory response and pain of osteoarthritis
Wei, K., Shu, Z., Pu, H., Xu, H., Li, S., Xiao, J., Zhu, Y., & Ma, T. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110289 · Cited by 20 · see citing works
Zhang, Y., & Zhou, Y. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117314 · Cited by 20 · see citing works
Nong, J., Lu, G., Huang, Y., Liu, J., Chen, L., Pan, H., & Xiong, B. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1178794 · Cited by 19 · see citing works
Chatterjee, P., Stevens, H. Y., Kippner, L. E., Bowles, A. C., Drissi, H., Mautner, K., Yeago, C., Gibson, G. C., & Roy, K. (2024) · iScience · doi:10.1016/j.isci.2024.110827 · Cited by 19 · see citing works
CDK8 mediated inflammatory microenvironment aggravates osteoarthritis progression
Lin, Z., Xu, Y., Jiang, H., Zeng, W., Wang, Y., Zhu, L., Lin, C., Lou, C., Shen, H., Ye, H., et al. (2025) · Journal of Advanced Research · doi:10.1016/j.jare.2025.01.017 · Cited by 21 · see citing works
Conway, J., Certo, M., Lord, J. M., Mauro, C., & Duggal, N. A. (2021) · British Journal of Pharmacology · doi:10.1111/bph.15671 · Cited by 19 · see citing works
Li, N., Luo, R., Zhang, W., Wu, Y., Hu, C., Liu, M., Jiang, D., Jiang, Z., Zhao, X., Wang, Y., et al. (2022) · Biogerontology · doi:10.1007/s10522-022-09999-2 · Cited by 19 · see citing works
Ji, M.-L., Li, Z., Hu, X. Y., Zhang, W. T., Zhang, H. X., & Lu, J. (2023) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2023.02.011 · Cited by 19 · see citing works
Self-citationLiu, W., Chen, Y., Zeng, G., Yang, S., Yang, T., Ma, M., & Song, W. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.748360 · Cited by 19 · see citing works
Huang, J., Bu, Z., Liu, W., Zhou, Z., Hu, J., Yu, J., Wang, H., Xu, S., & Wu, P. (2024) · Materials Today Bio · doi:10.1016/j.mtbio.2024.101124 · Cited by 18 · see citing works
In Vitro Study of the Therapeutic Potential of Brown Crude Fucoidans in Osteoarthritis Treatment
Vaamonde‐García, C., Capelo-Mera, E., Flórez-Fernández, N., Torres, M. D., Rivas‐Murias, B., Meijide-Faílde, R., Blanco, F. J., & Domı́nguez, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232214236 · Cited by 18 · see citing works
- Authors
- Faust, H. J., Zhang, H., Han, J., Wolf, M. T., Jeon, O. H., Sadtler, K., Peña, A. N., Chung, L., Maestas, D. R., Tam, A. J., Pardoll, D. M., Campisi, J., Housseau, F., Zhou, D., Bingham, C. O., & Elisseeff, J. H.
- Affiliations
- Johns Hopkins University (US)
- Korea University (KR)
- Buck Institute for Research on Aging (US)
- University of Florida (US)
- Corresponding author
- Elisseeff, Jennifer H.
- ORCID
- Venue
- Journal of Clinical Investigation
- Published
- 2020-09-21
- Volume
- 130
- Issue
- 10
- Pages
- 5493-5507
- ISSN
- 0021-9738 (ISSN-L)
- 1558-8238
- PMC
- PMC7524483
- OpenAlex
- W3087504560
- Cited by
- 260
- References
- 80
- Citations by year
- 2026: 33 · 2025: 56 · 2024: 57 · 2023: 46 · 2022: 43 · 2021: 24 · 2020: 1
- FWCI
- 21.64
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- other-oa
- Locations
- Journal of Clinical Investigation (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Defense (W81XWH-17-1-0627, W81XWH-14-1-0285)
- National Institutes of Health (R01CA211963, R01CA219836)
- Topics
- Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and 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
- osteoarthritis, senescence-associated secretory phenotype, senescence, IL-17, Th17 cells, post-traumatic osteoarthritis, anterior cruciate ligament transection, senolysis, p16INK4a, p21, innate lymphoid cells, γδ T cells, CD4+ T cells, TGF-beta, Wnt signaling, joint degeneration, aging, tissue repair
- MeSH terms
- Aging, Animals, Arthritis, Experimental, Disease Models, Animal, Humans, Immunity, Innate, Male, Mice, Inbred C57BL, Osteoarthritis, Cellular Senescence, Mice, Knockout, Receptors, Interleukin-4, Interleukin-17, Regenerative Medicine, Mice, Adaptive Immunity, Th17 Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review