TY - JOUR
T1 - Impacts of liver macrophages, gut microbiota, and bile acid metabolism on the differences in iHFC diet-induced MASH progression between TSNO and TSOD mice
AU - Igarashi, Naoya
AU - Kasai, Kaichi
AU - Tada, Yuki
AU - Kani, Koudai
AU - Kato, Miyuna
AU - Takano, Shun
AU - Goto, Kana
AU - Matsuura, Yudai
AU - Ichimura-Shimizu, Mayuko
AU - Watanabe, Shiro
AU - Tsuneyama, Koichi
AU - Furusawa, Yukihiro
AU - Nagai, Yoshinori
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2024.
PY - 2024/7
Y1 - 2024/7
N2 - Background: Tsumura-Suzuki non-obese (TSNO) mice exhibit a severe form of metabolic dysfunction-associated steatohepatitis (MASH) with advanced liver fibrosis upon feeding a high-fat/cholesterol/cholate-based (iHFC) diet. Another ddY strain, Tsumura-Suzuki diabetes obese (TSOD) mice, are impaired in the progression of iHFC diet-induced MASH. Aim: To elucidate the underlying mechanisms contributing to the differences in MASH progression between TSNO and TSOD mice. Methods: We analyzed differences in the immune system, gut microbiota, and bile acid metabolism in TSNO and TSOD mice fed with a normal diet (ND) or an iHFC diet. Results: TSOD mice had more anti-inflammatory macrophages in the liver than TSNO mice under ND feeding, and were impaired in the iHFC diet-induced accumulation of fibrosis-associated macrophages and formation of histological hepatic crown-like structures in the liver. The gut microbiota of TSOD mice also exhibited a distinct community composition with lower diversity and higher abundance of Akkermansia muciniphila compared with that in TSNO mice. Finally, TSOD mice had lower levels of bile acids linked to intestinal barrier disruption under iHFC feeding. Conclusions: The dynamics of liver macrophage subsets, and the compositions of the gut microbiota and bile acids at steady state and post-onset of MASH, had major impacts on MASH development.
AB - Background: Tsumura-Suzuki non-obese (TSNO) mice exhibit a severe form of metabolic dysfunction-associated steatohepatitis (MASH) with advanced liver fibrosis upon feeding a high-fat/cholesterol/cholate-based (iHFC) diet. Another ddY strain, Tsumura-Suzuki diabetes obese (TSOD) mice, are impaired in the progression of iHFC diet-induced MASH. Aim: To elucidate the underlying mechanisms contributing to the differences in MASH progression between TSNO and TSOD mice. Methods: We analyzed differences in the immune system, gut microbiota, and bile acid metabolism in TSNO and TSOD mice fed with a normal diet (ND) or an iHFC diet. Results: TSOD mice had more anti-inflammatory macrophages in the liver than TSNO mice under ND feeding, and were impaired in the iHFC diet-induced accumulation of fibrosis-associated macrophages and formation of histological hepatic crown-like structures in the liver. The gut microbiota of TSOD mice also exhibited a distinct community composition with lower diversity and higher abundance of Akkermansia muciniphila compared with that in TSNO mice. Finally, TSOD mice had lower levels of bile acids linked to intestinal barrier disruption under iHFC feeding. Conclusions: The dynamics of liver macrophage subsets, and the compositions of the gut microbiota and bile acids at steady state and post-onset of MASH, had major impacts on MASH development.
KW - Akkermansia muciniphila
KW - Bile acid
KW - Fibrosis
KW - Gut microbiota
KW - Macrophage
KW - Metabolic dysfunction associated steatohepatitis
UR - http://www.scopus.com/inward/record.url?scp=85190371538&partnerID=8YFLogxK
U2 - 10.1007/s00011-024-01884-7
DO - 10.1007/s00011-024-01884-7
M3 - 学術論文
C2 - 38619583
AN - SCOPUS:85190371538
SN - 1023-3830
VL - 73
SP - 1081
EP - 1098
JO - Inflammation Research
JF - Inflammation Research
IS - 7
ER -