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Gas6 ameliorates intestinal mucosal immunosenescence to prevent the translocation of a gut pathobiont, Klebsiella pneumoniae, to the liver.
Tsugawa, Hitoshi; Ohki, Takuto; Tsubaki, Shogo; Tanaka, Rika; Matsuzaki, Juntaro; Suzuki, Hidekazu; Hozumi, Katsuto.
Affiliation
  • Tsugawa H; Transkingdom Signaling Research Unit, Division of Host Defense Mechanism, Tokai University School of Medicine, Isehara, Japan.
  • Ohki T; Department of Hand Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Tsubaki S; Transkingdom Signaling Research Unit, Division of Host Defense Mechanism, Tokai University School of Medicine, Isehara, Japan.
  • Tanaka R; Department of Immunology, Division of Host Defense Mechanism, Tokai University School of Medicine, Isehara, Japan.
  • Matsuzaki J; Division of Pharmacotherapeutics, Keio University Faculty of Pharmacy, Tokyo, Japan.
  • Suzuki H; Division of Gastroenterology and Hepatology, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Hozumi K; Department of Immunology, Division of Host Defense Mechanism, Tokai University School of Medicine, Isehara, Japan.
PLoS Pathog ; 19(6): e1011139, 2023 Jun.
Article in En | MEDLINE | ID: mdl-37289655
ABSTRACT
Immunosenescence refers to the development of weakened and/or dysfunctional immune responses associated with aging. Several commensal bacteria can be pathogenic in immunosuppressed individuals. Although Klebsiella pneumoniae is a commensal bacterium that colonizes human mucosal surfaces, the gastrointestinal tract, and the oropharynx, it can cause serious infectious diseases, such as pneumonia, urinary tract infections, and liver abscesses, primarily in elderly patients. However, the reason why K. pneumoniae is a more prevalent cause of infection in the elderly population remains unclear. This study aimed to determine how the host's intestinal immune response to K. pneumoniae varies with age. To this end, the study analyzed an in vivo K. pneumoniae infection model using aged mice, as well as an in vitro K. pneumoniae infection model using a Transwell insert co-culture system comprising epithelial cells and macrophages. In this study, we demonstrate that growth arrest-specific 6 (Gas6), released by intestinal macrophages that recognize K. pneumoniae, inhibits bacterial translocation from the gastrointestinal tract by enhancing tight-junction barriers in the intestinal epithelium. However, in aging mice, Gas6 was hardly secreted under K. pneumoniae infection due to decreasing intestinal mucosal macrophages; therefore, K. pneumoniae can easily invade the intestinal epithelium and subsequently translocate to the liver. Moreover, the administration of Gas6 recombinant protein to elderly mice prevented the translocation of K. pneumoniae from the gastrointestinal tract and significantly prolonged their survival. From these findings, we conclude that the age-related decrease in Gas6 secretion in the intestinal mucosa is the reason why K. pneumoniae can be pathogenic in the elderly, thereby indicating that Gas6 could be effective in protecting the elderly against infectious diseases caused by gut pathogens.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Klebsiella Infections / Communicable Diseases / Immunosenescence Type of study: Prognostic_studies Limits: Aged / Animals / Humans Language: En Journal: PLoS Pathog Year: 2023 Type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Klebsiella Infections / Communicable Diseases / Immunosenescence Type of study: Prognostic_studies Limits: Aged / Animals / Humans Language: En Journal: PLoS Pathog Year: 2023 Type: Article Affiliation country: Japan