MicroRNA-mediated Regulation of the Development and Functions of Follicular Helper T cells
2
조회
0
다운로드
2
인용
0
참고문헌
키워드
초록
The germinal center reaction is a key event of humoral immunity, providing long-lived immunological memory. Follicular helper T (TFH) cells are a specialized subset of CD4+ T cells located in the follicles, which help B cells and thus control the germinal center reaction. TFH cell development is achieved by multi-step processes of interactions with dendritic cells and B cells along with the coordination of various transcription factors. Since the T helper cell fate decision program is determined by subtle changes in regulatory molecules, fine tuning of these dynamic interactions is crucial for the generation functional TFH cells. MicroRNAs (miRNAs) have emerged as important post-transcriptional regulatory molecules for gene expression, which consequently modulate diverse biological functions. In the last decade, the miRNA-mediated regulation network for the germinal center reaction has been extensively explored in T cells and B cells, resulting in the identification of several key miRNA species and their target genes. Here, we review the current knowledge of the miRNA-mediated control of the germinal center reaction, focusing on the aspect of T cell regulation in particular. In addition, we highlight the most important issues related to defining the functional target genes of the relevant miRNAs. We believe that the studies that uncover the miRNA-mediated regulatory axis of TFH cell generation and functions by defining their functional target genes might provide additional opportunities to understand germinal center reactions.
Abstract
The germinal center reaction is a key event of humoral immunity, providing long-lived immunological memory. Follicular helper T (TFH) cells are a specialized subset of CD4+ T cells located in the follicles, which help B cells and thus control the germinal center reaction. TFH cell development is achieved by multi-step processes of interactions with dendritic cells and B cells along with the coordination of various transcription factors. Since the T helper cell fate decision program is determined by subtle changes in regulatory molecules, fine tuning of these dynamic interactions is crucial for the generation functional TFH cells. MicroRNAs (miRNAs) have emerged as important post-transcriptional regulatory molecules for gene expression, which consequently modulate diverse biological functions. In the last decade, the miRNA-mediated regulation network for the germinal center reaction has been extensively explored in T cells and B cells, resulting in the identification of several key miRNA species and their target genes. Here, we review the current knowledge of the miRNA-mediated control of the germinal center reaction, focusing on the aspect of T cell regulation in particular. In addition, we highlight the most important issues related to defining the functional target genes of the relevant miRNAs. We believe that the studies that uncover the miRNA-mediated regulatory axis of TFH cell generation and functions by defining their functional target genes might provide additional opportunities to understand germinal center reactions.
참고문헌 (58)
- Bortnick A, "What is and what should always have been: long-lived plasma cells induced by T cell-independent antigens", J Immunol, 190, pp.5913~5918 (2013)[DOI]
- Racine R, "IgM in microbial infections: taken for granted?", Immunol Lett, 125, pp.79~85 (2009)[DOI]
- Vinuesa CG, "Dysregulation of germinal centres in autoimmune disease", Nat Rev Immunol, 9, pp.845~857 (2009)[DOI]
- Basso K, "Germinal centres and B cell lymphomagenesis", Nat Rev Immunol, 15, pp.172~184 (2015)[DOI]
- Kim CH, "Subspecialization of CXCR5+ T cells: B helper activity is focused in a germinal center-localized subset of CXCR5+ T cells", J Exp Med, 193, pp.1373~1381 (2001)[DOI]
- Campbell DJ, "Separable effector T cell populations specialized for B cell help or tissue inflammation", Nat Immunol, 2, pp.876~881 (2001)[DOI]
- Crotty S, "T follicular helper cell differentiation, function, and roles in disease", Immunity, 41, pp.529~542 (2014)[DOI]
- Pratama A, "Control of TFH cell numbers: why and how?", Immunol Cell Biol, 92, pp.40~48 (2014)[DOI]
- Blanco P, "T follicular helper (Tfh) cells in lupus: activation and involvement in SLE pathogenesis", Eur J Immunol, 46, pp.281~290 (2016)[DOI]
- Ueno H, "Pathophysiology of T follicular helper cells in humans and mice", Nat Immunol, 16, pp.142~152 (2015)[DOI]
- Choi YS, "ICOS receptor instructs T follicular helper cell versus effector cell differentiation via induction of the transcriptional repressor Bcl6", Immunity, 34, pp.932~946 (2011)[DOI]
- Liu X, "Transcription factor achaete-scute homologue 2 initiates follicular T-helper-cell development", Nature, 507, pp.513~518 (2014)[DOI]
- Li J, "EBI2 augments Tfh cell fate by promoting interaction with IL-2-quenching dendritic cells", Nature, 533, pp.110~114 (2016)[DOI]
- Johnston RJ, "STAT5 is a potent negative regulator of TFH cell differentiation", J Exp Med, 209, pp.243~250 (2012)[DOI]
- Nurieva RI, "STAT5 protein negatively regulates T follicular helper (Tfh) cell generation and function", J Biol Chem, 287, pp.11234~11239 (2012)[DOI]
- Xu H, "Follicular T-helper cell recruitment governed by bystander B cells and ICOS-driven motility", Nature, 496, pp.523~527 (2013)[DOI]
- Liu X, "Transcriptional regulation of follicular T-helper (Tfh) cells", Immunol Rev, 252, pp.139~145 (2013)[DOI]
- Fang D, "Dynamic balance between master transcription factors determines the fates and functions of CD4 T cell and innate lymphoid cell subsets", J Exp Med, 214, pp.1861~1876 (2017)[DOI]
- Chekulaeva M, "Mechanisms of miRNA-mediated post-transcriptional regulation in animal cells", Curr Opin Cell Biol, 21, pp.452~460 (2009)[DOI]
- Rupaimoole R, "MicroRNA therapeutics: towards a new era for the management of cancer and other diseases", Nat Rev Drug Discov, 16, pp.203~222 (2017)[DOI]
- Kuchen S, "Regulation of microRNA expression and abundance during lymphopoiesis", Immunity, 32, pp.828~839 (2010)[DOI]
- Landgraf P, "A mammalian microRNA expression atlas based on small RNA library sequencing", Cell, 129, pp.1401~1414 (2007)[DOI]
- Bronevetsky Y, "T cell activation induces proteasomal degradation of Argonaute and rapid remodeling of the microRNA repertoire", J Exp Med, 210, pp.417~432 (2013)[DOI]
- Pratama A, "MicroRNA-146a regulates ICOS-ICOSL signalling to limit accumulation of T follicular helper cells and germinal centres", Nat Commun, 6, pp.6436~ (2015)[DOI]
- Muljo SA, "Aberrant T cell differentiation in the absence of Dicer", J Exp Med, 202, pp.261~269 (2005)[DOI]
- Steiner DF, "MicroRNA-29 regulates T-box transcription factors and interferon-<TEX>$\gamma$<", TEX> production in helper T cells, 2011, pp.35, 169~181
- Baumjohann D, "The microRNA cluster miR-17-92 promotes TFH cell differentiation and represses subset-inappropriate gene expression", Nat Immunol, 14, pp.840~848 (2013)[DOI]
- Kang SG, "MicroRNAs of the miR-17-92 family are critical regulators of T(FH) differentiation", Nat Immunol, 14, pp.849~857 (2013)[DOI]
- Liu WH, "A miR-155-Peli1-c-Rel pathway controls the generation and function of T follicular helper cells", J Exp Med, 213, pp.1901~1919 (2016)[DOI]
- Yu D, "The transcriptional repressor Bcl-6 directs T follicular helper cell lineage commitment", Immunity, 31, pp.457~468 (2009)[DOI]
- Rodriguez A, "Requirement of bic", microRNA-155 for normal immune function, 2007, pp.316, 608~611
- Hu R, "miR-155 promotes T follicular helper cell accumulation during chronic, low-grade inflammation", Immunity, 41, pp.605~619 (2014)[DOI]
- Chang M, "The ubiquitin ligase Peli1 negatively regulates T cell activation and prevents autoimmunity", Nat Immunol, 12, pp.1002~1009 (2011)[DOI]
- Stittrich AB, "The microRNA miR-182 is induced by IL-2 and promotes clonal expansion of activated helper T lymphocytes", Nat Immunol, 11, pp.1057~1062 (2010)[DOI]
- Stone EL, "ICOS coreceptor signaling inactivates the transcription factor FOXO1 to promote Tfh cell differentiation", Immunity, 42, pp.239~251 (2015)[DOI]
- Sakaguchi S, "Naturally arising CD4+ regulatory t cells for immunologic self-tolerance and negative control of immune responses", Annu Rev Immunol, 22, pp.531~562 (2004)[DOI]
- Levine AG, "Stability and function of regulatory T cells expressing the transcription factor T-bet", Nature, 546, pp.421~425 (2017)[DOI]
- Yang BH, "Foxp3(+) T cells expressing <TEX>$ROR{\gamma}t$<", TEX> represent a stable regulatory T-cell effector lineage with enhanced suppressive capacity during intestinal inflammation, 2016, pp.9, 444~457
- Chung Y, "Follicular regulatory T cells expressing Foxp3 and Bcl-6 suppress germinal center reactions", Nat Med, 17, pp.983~988 (2011)[DOI]
- Linterman MA, "Foxp3+ follicular regulatory T cells control the germinal center response", Nat Med, 17, pp.975~982 (2011)[DOI]
- Linterman MA, "T-follicular helper cell differentiation and the co-option of this pathway by non-helper cells", Immunol Rev, 247, pp.143~159 (2012)[DOI]
- Lu LF, "Function of miR-146a in controlling Treg cell-mediated regulation of Th1 responses", Cell, 142, pp.914~929 (2010)[DOI]
- Kohlhaas S, "Cutting edge: the Foxp3 target miR-155 contributes to the development of regulatory T cells", J Immunol, 182, pp.2578~2582 (2009)[DOI]
- Lu LF, "Foxp3-dependent microRNA155 confers competitive fitness to regulatory T cells by targeting SOCS1 protein", Immunity, 30, pp.80~91 (2009)[DOI]
- Takahashi H, "TGF-<TEX>${\beta}$<", TEX> and retinoic acid induce the microRNA miR-10a, which targets Bcl-6 and constrains the plasticity of helper T cells, 2012, pp.13, 587~595
- Jeker LT, "MicroRNA 10a marks regulatory T cells", PLoS One, 7, pp.e36684~ (2012)[DOI]
- Baumjohann D, "MicroRNA regulation of the germinal center response", Curr Opin Immunol, 28, pp.6~11 (2014)[DOI]
- Wu T, "Cutting edge: mir-17-92 is required for both CD4 Th1 and T follicular helper cell responses during viral infection", J Immunol, 195, pp.2515~2519 (2015)[DOI]
- Jiang S, "Molecular dissection of the miR-17-92 cluster's critical dual roles in promoting Th1 responses and preventing inducible Treg differentiation", Blood, 118, pp.5487~5497 (2011)[DOI]
- Escobar TM, "miR-155 activates cytokine gene expression in Th17 cells by regulating the DNA-binding protein Jarid2 to relieve polycomb-mediated repression", Immunity, 40, pp.865~879 (2014)[DOI]
- Hu R, "MicroRNA-155 confers encephalogenic potential to Th17 cells by promoting effector gene expression", J Immunol, 190, pp.5972~5980 (2013)[DOI]
- Lu LF, "A single miRNA-mRNA interaction affects the immune response in a context- and cell-type-specific manner", Immunity, 43, pp.52~64 (2015)[DOI]
- Zawislak CL, "Stage-specific regulation of natural killer cell homeostasis and response against viral infection by microRNA-155", Proc Natl Acad Sci U S A, 110, pp.6967~6972 (2013)[DOI]
- Lai X, "Understanding microRNA-mediated gene regulatory networks through mathematical modelling", Nucleic Acids Res, 44, pp.6019~6035 (2016)[DOI]
- Jin HY, "MicroRNA mechanisms of action: what have we learned from mice?", Front Genet, 6, pp.328~ (2015)
- Jin HY, "Differential sensitivity of target genes to translational repression by miR-17-92", PLoS Genet, 13, pp.e1006623~ (2017)[DOI]
- Hale JS, "Memory T follicular helper CD4 T cells", Front Immunol, 6, pp.16~ (2015)
- Shane Crotty, "Do Memory CD4 T Cells Keep Their Cell-Type Programming: Plasticity versus Fate Commitment?", Cold Spring Harbor Perspectives in Biology, 10(3), pp.a032102~ (2018), Cold Spring Harbor Laboratory[DOI]
