Unconventional immune cells in the gut mucosal barrier: regulation by symbiotic microbiota
The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-ch...
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Published in | Experimental & molecular medicine Vol. 55; no. 9; pp. 1905 - 1912 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.09.2023
Springer Nature B.V Nature Publishing Group 생화학분자생물학회 |
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Abstract | The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-characterized innate and adaptive immune cells, a growing body of evidence shows additional important players in gut mucosal immunity. Among them, unconventional immune cells, including innate lymphoid cells (ILCs) and unconventional T cells, are essential for maintaining homeostasis. These cells rapidly respond to bacterial signals and bridge the innate immunity and adaptive immunity in the mucosal barrier. Here, we focus on the types and roles of these immune cells in physiological and pathological conditions as prominent mechanisms by which the host immune system communicates with the gut microbiota in health and diseases.
Bridging the gap: immunity and gut microbiota
This study highlights the essential role of microbiota in regulating the maintenance and function of ILC subsets and unconventional T cells in the gut. Microbial colonization influences cytokine production, affecting ILC function in barrier maintenance and protection against pathogens. Additionally, microbiota-derived antigens shape MAIT and iNKT cell populations, with their activity finely regulated by a combination of metabolites and local cytokines influenced by the microbiota. Understanding these interactions could lead to innovative strategies for enhancing gut health and effectively treating immune-mediated diseases. |
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AbstractList | The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-characterized innate and adaptive immune cells, a growing body of evidence shows additional important players in gut mucosal immunity. Among them, unconventional immune cells, including innate lymphoid cells (ILCs) and unconventional T cells, are essential for maintaining homeostasis. These cells rapidly respond to bacterial signals and bridge the innate immunity and adaptive immunity in the mucosal barrier. Here, we focus on the types and roles of these immune cells in physiological and pathological conditions as prominent mechanisms by which the host immune system communicates with the gut microbiota in health and diseases. The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-characterized innate and adaptive immune cells, a growing body of evidence shows additional important players in gut mucosal immunity. Among them, unconventional immune cells, including innate lymphoid cells (ILCs) and unconventional T cells, are essential for maintaining homeostasis. These cells rapidly respond to bacterial signals and bridge the innate immunity and adaptive immunity in the mucosal barrier. Here, we focus on the types and roles of these immune cells in physiological and pathological conditions as prominent mechanisms by which the host immune system communicates with the gut microbiota in health and diseases.Bridging the gap: immunity and gut microbiotaThis study highlights the essential role of microbiota in regulating the maintenance and function of ILC subsets and unconventional T cells in the gut. Microbial colonization influences cytokine production, affecting ILC function in barrier maintenance and protection against pathogens. Additionally, microbiota-derived antigens shape MAIT and iNKT cell populations, with their activity finely regulated by a combination of metabolites and local cytokines influenced by the microbiota. Understanding these interactions could lead to innovative strategies for enhancing gut health and effectively treating immune-mediated diseases. The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-characterized innate and adaptive immune cells, a growing body of evidence shows additional important players in gut mucosal immunity. Among them, unconventional immune cells, including innate lymphoid cells (ILCs) and unconventional T cells, are essential for maintaining homeostasis. These cells rapidly respond to bacterial signals and bridge the innate immunity and adaptive immunity in the mucosal barrier. Here, we focus on the types and roles of these immune cells in physiological and pathological conditions as prominent mechanisms by which the host immune system communicates with the gut microbiota in health and diseases. This study highlights the essential role of microbiota in regulating the maintenance and function of ILC subsets and unconventional T cells in the gut. Microbial colonization influences cytokine production, affecting ILC function in barrier maintenance and protection against pathogens. Additionally, microbiota-derived antigens shape MAIT and iNKT cell populations, with their activity finely regulated by a combination of metabolites and local cytokines influenced by the microbiota. Understanding these interactions could lead to innovative strategies for enhancing gut health and effectively treating immune-mediated diseases. Abstract The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-characterized innate and adaptive immune cells, a growing body of evidence shows additional important players in gut mucosal immunity. Among them, unconventional immune cells, including innate lymphoid cells (ILCs) and unconventional T cells, are essential for maintaining homeostasis. These cells rapidly respond to bacterial signals and bridge the innate immunity and adaptive immunity in the mucosal barrier. Here, we focus on the types and roles of these immune cells in physiological and pathological conditions as prominent mechanisms by which the host immune system communicates with the gut microbiota in health and diseases. The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-characterized innate and adaptive immune cells, a growing body of evidence shows additional important players in gut mucosal immunity. Among them, unconventional immune cells, including innate lymphoid cells (ILCs) and unconventional T cells, are essential for maintaining homeostasis. These cells rapidly respond to bacterial signals and bridge the innate immunity and adaptive immunity in the mucosal barrier. Here, we focus on the types and roles of these immune cells in physiological and pathological conditions as prominent mechanisms by which the host immune system communicates with the gut microbiota in health and diseases. KCI Citation Count: 0 The mammalian gut is the most densely colonized organ by microbial species, which are in constant contact with the host throughout life. Hosts have developed multifaceted cellular and molecular mechanisms to distinguish and respond to benign and pathogenic bacteria. In addition to relatively well-characterized innate and adaptive immune cells, a growing body of evidence shows additional important players in gut mucosal immunity. Among them, unconventional immune cells, including innate lymphoid cells (ILCs) and unconventional T cells, are essential for maintaining homeostasis. These cells rapidly respond to bacterial signals and bridge the innate immunity and adaptive immunity in the mucosal barrier. Here, we focus on the types and roles of these immune cells in physiological and pathological conditions as prominent mechanisms by which the host immune system communicates with the gut microbiota in health and diseases. Bridging the gap: immunity and gut microbiota This study highlights the essential role of microbiota in regulating the maintenance and function of ILC subsets and unconventional T cells in the gut. Microbial colonization influences cytokine production, affecting ILC function in barrier maintenance and protection against pathogens. Additionally, microbiota-derived antigens shape MAIT and iNKT cell populations, with their activity finely regulated by a combination of metabolites and local cytokines influenced by the microbiota. Understanding these interactions could lead to innovative strategies for enhancing gut health and effectively treating immune-mediated diseases. |
Author | Oh, Sungwhan F. Yoo, Ji-Sun |
Author_xml | – sequence: 1 givenname: Ji-Sun surname: Yoo fullname: Yoo, Ji-Sun organization: Center for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women’s Hospital – sequence: 2 givenname: Sungwhan F. orcidid: 0000-0002-0280-7903 surname: Oh fullname: Oh, Sungwhan F. email: soh2@bwh.harvard.edu organization: Center for Experimental Therapeutics and Reperfusion Injury, Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women’s Hospital, Graduate Program in Immunology, Harvard Medical School |
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Title | Unconventional immune cells in the gut mucosal barrier: regulation by symbiotic microbiota |
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ispartofPNX | Experimental and Molecular Medicine, 2023, 55(0), , pp.1905-1912 |
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