| Autor: |
Liu Y; the University of Texas Health Science Center at Houston., Armbrister SA; the University of Texas Health Science Center at Houston., Okeugo B; the University of Texas Health Science Center at Houston., Mills TW; the University of Texas Health Science Center at Houston., Daniel RC; the University of Texas Health Science Center at Houston., Oh JH; University of Wisconsin-Madison., Pijkeren JP; University of Wisconsin-Madison., Park ES; the University of Texas Health Science Center at Houston., Saleh ZM; the University of Texas Health Science Center at Houston., Lahiri S; the University of Texas Health Science Center at Houston., Roos S; Uppsala BioCenter, Swedish Univeristy of Agricultural Sciences., Rhoads JM; the University of Texas Health Science Center at Houston. |
| Jazyk: |
angličtina |
| Zdroj: |
Research square [Res Sq] 2023 Apr 07. Date of Electronic Publication: 2023 Apr 07. |
| DOI: |
10.21203/rs.3.rs-2781715/v1 |
| Abstrakt: |
Probiotic Limosilactobacillus reuteri DSM 17938 (DSM 17938) prolonges the survival of Treg-deficient scurfy (SF) mice and reduces multiorgan inflammation by a process requiring adenosine receptor 2A (A 2A ) on T cells. We hypothesized that L. reuteri -derived ecto-5'-nucleotidase (ecto-5'NT) activity acts to generate adenosine, which may be a central mediator for L. reuteri protection in SF mice. We evaluated DSM 17938-5'NT activity and the associated adenosine and inosine levels in plasma, gut and liver of SF mice. We examined orally fed DSM 17938, DSM 17938Δ5NT (with a deleted 5'NT gene), and DSM 32846 (BG-R46) (a naturally selected strain derived from DSM 17938). Results showed that DSM 17938 and BG-R46 produced adenosine while "exhausting" AMP, whereas DSM 17938∆5NT did not generate adenosine in culture. Plasma 5'NT activity was increased by DSM 17938 or BG-R46, but not by DSM 17938Δ5NT in SF mice. BG-R46 increased both adenosine and inosine levels in the cecum of SF mice. DSM 17938 increased adenosine levels, whereas BG-R46 increased inosine levels in the liver. DSM 17938Δ5NT did not significantly change the levels of adenosine or inosine in the GI tract or the liver of SF mice. Although regulatory CD73 + CD8 + T cells were decreased in spleen and blood of SF mice, these regulatory T cells could be increased by orally feeding DSM 17938 or BG-R46, but not DSM 17938Δ5NT. In conclusion, probiotic-5'NT may be a central mediator of DSM 17938 protection against autoimmunity. Optimal 5'NT activity from various probiotic strains could be beneficial in treating Treg-associated immune disorders in humans. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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