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      Sertoli Cell Immune Regulation: A Double-Edged Sword

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          Abstract

          The testis must create and maintain an immune privileged environment to protect maturing germ cells from autoimmune destruction. The establishment of this protective environment is due, at least in part, to Sertoli cells. Sertoli cells line the seminiferous tubules and form the blood-testis barrier (BTB), a barrier between advanced germ cells and the immune system. The BTB compartmentalizes the germ cells and facilitates the appropriate microenvironment necessary for spermatogenesis. Further, Sertoli cells modulate innate and adaptive immune processes through production of immunoregulatory compounds. Sertoli cells, when transplanted ectopically (outside the testis), can also protect transplanted tissue from the recipient’s immune system and reduce immune complications in autoimmune diseases primarily by immune regulation. These properties make Sertoli cells an attractive candidate for inflammatory disease treatments and cell-based therapies. Conversely, the same properties that protect the germ cells also allow the testis to act as a reservoir site for infections. Interestingly, Sertoli cells also have the ability to mount an antimicrobial response, if necessary, as in the case of infections. This review aims to explore how Sertoli cells act as a double-edged sword to both protect germ cells from an autoimmune response and activate innate and adaptive immune responses to fight off infections.

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          NF-κB signaling in inflammation

          The transcription factor NF-κB regulates multiple aspects of innate and adaptive immune functions and serves as a pivotal mediator of inflammatory responses. NF-κB induces the expression of various pro-inflammatory genes, including those encoding cytokines and chemokines, and also participates in inflammasome regulation. In addition, NF-κB plays a critical role in regulating the survival, activation and differentiation of innate immune cells and inflammatory T cells. Consequently, deregulated NF-κB activation contributes to the pathogenic processes of various inflammatory diseases. In this review, we will discuss the activation and function of NF-κB in association with inflammatory diseases and highlight the development of therapeutic strategies based on NF-κB inhibition.
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            IL-6 in inflammation, immunity, and disease.

            Interleukin 6 (IL-6), promptly and transiently produced in response to infections and tissue injuries, contributes to host defense through the stimulation of acute phase responses, hematopoiesis, and immune reactions. Although its expression is strictly controlled by transcriptional and posttranscriptional mechanisms, dysregulated continual synthesis of IL-6 plays a pathological effect on chronic inflammation and autoimmunity. For this reason, tocilizumab, a humanized anti-IL-6 receptor antibody was developed. Various clinical trials have since shown the exceptional efficacy of tocilizumab, which resulted in its approval for the treatment of rheumatoid arthritis and juvenile idiopathic arthritis. Moreover, tocilizumab is expected to be effective for other intractable immune-mediated diseases. In this context, the mechanism for the continual synthesis of IL-6 needs to be elucidated to facilitate the development of more specific therapeutic approaches and analysis of the pathogenesis of specific diseases.
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              Toll-Like Receptor Signaling Pathways

              Toll-like receptors (TLRs) play crucial roles in the innate immune system by recognizing pathogen-associated molecular patterns derived from various microbes. TLRs signal through the recruitment of specific adaptor molecules, leading to activation of the transcription factors NF-κB and IRFs, which dictate the outcome of innate immune responses. During the past decade, the precise mechanisms underlying TLR signaling have been clarified by various approaches involving genetic, biochemical, structural, cell biological, and bioinformatics studies. TLR signaling appears to be divergent and to play important roles in many aspects of the innate immune responses to given pathogens. In this review, we describe recent progress in our understanding of TLR signaling regulation and its contributions to host defense.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                09 June 2022
                2022
                : 13
                : 913502
                Affiliations
                [1] 1 Department of Cell Biology and Biochemistry, Texas Tech University Health Sciences Center , Lubbock, TX, United States
                [2] 2 Immunology and Infectious Disease Concentration, Texas Tech University Health Sciences Center , Lubbock, TX, United States
                [3] 3 Department of Medical Education, Texas Tech University Health Sciences Center , Lubbock, TX, United States
                Author notes

                Edited by: Daishu Han, Chinese Academy of Medical Sciences and Peking Union Medical College, China

                Reviewed by: Wing-Yee Lui, The University of Hong Kong, Hong Kong SAR, China; Sudhanshu Bhushan, University of Giessen, Germany

                *Correspondence: Jannette M. Dufour, jannette.dufour@ 123456ttuhsc.edu

                †These authors have contributed equally to this work

                This article was submitted to Viral Immunology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2022.913502
                9218077
                35757731
                a70ba2d2-af0c-46d0-bb15-c27bed285094
                Copyright © 2022 Washburn, Hibler, Kaur and Dufour

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 05 April 2022
                : 29 April 2022
                Page count
                Figures: 4, Tables: 3, Equations: 0, References: 185, Pages: 19, Words: 11589
                Funding
                Funded by: National Institute of Allergy and Infectious Diseases , doi 10.13039/100000060;
                Funded by: CH Foundation , doi 10.13039/100001027;
                Categories
                Immunology
                Review

                Immunology
                sertoli cells,immune regulation,transplantation,cell therapeutics,testis
                Immunology
                sertoli cells, immune regulation, transplantation, cell therapeutics, testis

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