9
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      The GSK3β-β-catenin-TCF1 pathway improves naive T cell activation in old adults by upregulating miR-181a

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          MicroRNAs play an important role in the regulation of T cell development, activation, and differentiation. One of the most abundant microRNAs in lymphocytes is miR-181a, which controls T cell receptor (TCR) activation thresholds in thymic selection as well as in peripheral T cell responses. We previously found that miR-181a levels decline in T cells in the elderly. In this study, we identified TCF1 as a transcriptional regulator of pri-miR-181a. A decline in TCF1 levels in old individuals accounted for the reduced miR-181a expression impairing TCR signaling. Inhibition of GSK3ß restored expression of miR-181a by inducing TCF1 in T cells from old adults. GSK3ß inhibition enhanced TCR signaling to increase downstream expression of activation markers and production of IL-2. The effect involved the upregulation of miR-181a and the inhibition of DUSP6 expression. Thus, inhibition of GSK3ß can restore responses of old T cells by inducing miR-181a expression through TCF1.

          Related collections

          Most cited references46

          • Record: found
          • Abstract: not found
          • Article: not found

          Micromanagers of gene expression: the potentially widespread influence of metazoan microRNAs.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            T Cell Factor 1-Expressing Memory-like CD8(+) T Cells Sustain the Immune Response to Chronic Viral Infections.

            Chronic infections promote the terminal differentiation (or "exhaustion") of T cells and are thought to preclude the formation of memory T cells. In contrast, we discovered a small subpopulation of virus-specific CD8(+) T cells that sustained the T cell response during chronic infections. These cells were defined by, and depended on, the expression of the transcription factor Tcf1. Transcriptome analysis revealed that this population shared key characteristics of central memory cells but lacked an effector signature. Unlike conventional memory cells, Tcf1-expressing T cells displayed hallmarks of an "exhausted" phenotype, including the expression of inhibitory receptors such as PD-1 and Lag-3. This population was crucial for the T cell expansion that occurred in response to inhibitory receptor blockade during chronic infection. These findings identify a memory-like T cell population that sustains T cell responses and is a prime target for therapeutic interventions to improve the immune response in chronic infections.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The twilight of immunity: emerging concepts in aging of the immune system

              Immunosenescence is a series of age-related changes that affect the immune system and, with time, lead to increased vulnerability to infectious diseases. This Review addresses recent developments in the understanding of age-related changes that affect key components of immunity, including the effect of aging on cells of the (mostly adaptive) immune system, on soluble molecules that guide the maintenance and function of the immune system and on lymphoid organs that coordinate both the maintenance of lymphocytes and the initiation of immune responses. I further address the effect of the metagenome and exposome as key modifiers of immune-system aging and discuss a conceptual framework in which age-related changes in immunity might also affect the basic rules by which the immune system operates.
                Bookmark

                Author and article information

                Contributors
                jgoronzy@stanford.edu
                Journal
                NPJ Aging Mech Dis
                NPJ Aging Mech Dis
                NPJ Aging and Mechanisms of Disease
                Nature Publishing Group UK (London )
                2056-3973
                8 February 2021
                8 February 2021
                2021
                : 7
                : 4
                Affiliations
                [1 ]GRID grid.168010.e, ISNI 0000000419368956, From the Department of Medicine, Division of Immunology and Rheumatology, , Stanford University, ; Stanford, CA 94305 USA
                [2 ]GRID grid.280747.e, ISNI 0000 0004 0419 2556, Department of Medicine, , Veterans Affairs Palo Alto Health Care System, ; Palo Alto, CA 94306 USA
                Author information
                http://orcid.org/0000-0002-6858-1265
                http://orcid.org/0000-0003-1143-9388
                http://orcid.org/0000-0003-2230-9802
                http://orcid.org/0000-0001-7670-1856
                Article
                56
                10.1038/s41514-021-00056-9
                7870817
                33558531
                d19582b9-09e3-4159-9b5c-f3a8e1253c66
                © This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 16 June 2020
                : 8 January 2021
                Funding
                Funded by: FundRef https://doi.org/10.13039/100005440, U.S. Department of Health & Human Services | NIH | Center for Scientific Review (NIH Center for Scientific Review);
                Award ID: R01 AR042527
                Award ID: R01 HL117913
                Award ID: R01 AI108906
                Award ID: P01 HL129941
                Award Recipient :
                Funded by: U.S. Department of Health & Human Services | NIH | Center for Scientific Review (NIH Center for Scientific Review)
                Funded by: U.S. Department of Health & Human Services | NIH | Center for Scientific Review (NIH Center for Scientific Review)
                Funded by: U.S. Department of Health & Human Services | NIH | Center for Scientific Review (NIH Center for Scientific Review)
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                transcription,cell signalling
                transcription, cell signalling

                Comments

                Comment on this article