Impact of Gut Recolonization on Liver Regeneration: Hepatic Matrisome Gene Expression after Partial Hepatectomy in Mice.
Abdul Rahman AminNgatiman M HairulhisyamRaman Nur Fatin AqilahMohd Manzor Nur FarihaBeth L MallardFergus ShanahanAntony M WheatleyMuhamad MarliniPublished in: International journal of molecular sciences (2023)
The hepatic matrisome is involved in the remodeling phase of liver regeneration. As the gut microbiota has been implicated in liver regeneration, we investigated its role in liver regeneration focusing on gene expression of the hepatic matrisome after partial hepatectomy (PHx) in germ-free (GF) mice, and in GF mice reconstituted with normal gut microbiota (XGF). Liver mass restoration, hepatocyte proliferation, and immune response were assessed following 70% PHx. Hepatic matrisome and collagen gene expression were also analyzed. Reduced liver weight/body weight ratio, mitotic count, and hepatocyte proliferative index at 72 h post PHx in GF mice were preceded by reduced expression of cytokine receptor genes Tnfrsf1a and Il6ra , and Hgf gene at 3 h post PHx. In XGF mice, these indices were significantly higher than in GF mice, and similar to that of control mice, indicating normal liver regeneration. Differentially expressed genes (DEGs) of the matrisome were lower in GF compared to XGF mice at both 3 h and 72 h post PHx. GF mice also demonstrated lower collagen expression, with significantly lower expression of Col1a1 , Col1a2 , Col5a1, and Col6a2 compared to WT mice at 72 h post PHx. In conclusion, enhanced liver regeneration and matrisome expression in XGF mice suggests that interaction of the gut microbiota and matrisome may play a significant role in the regulation of hepatic remodeling during the regenerative process.
Keyphrases
- gene expression
- stem cells
- high fat diet induced
- poor prognosis
- immune response
- dna methylation
- genome wide
- body weight
- body mass index
- rheumatoid arthritis
- binding protein
- cell proliferation
- wild type
- inflammatory response
- weight loss
- signaling pathway
- skeletal muscle
- physical activity
- toll like receptor
- mass spectrometry
- long non coding rna
- adipose tissue
- high resolution
- cell cycle
- liver injury
- insulin resistance
- copy number
- disease activity
- tissue engineering
- bioinformatics analysis
- genome wide analysis
- genome wide identification