Brain-derived neurotrophic factor knock-out mice develop non-alcoholic steatohepatitis.
Mayuko Ichimura-ShimizuMasami KojimaShingo SuzukiMisaki MiyataYui OsakiKonomi MatsuiToshiyuki MizuiKoichi TsuneyamaPublished in: The Journal of pathology (2023)
While brain-derived neurotrophic factor (BDNF), which is a growth factor associated with cognitive improvement and the alleviation of depression symptoms, is known to regulate food intake and body weight, the role of BDNF in peripheral disease is not fully understood. Here, we show that reduced BDNF expression is associated with weight gain and the chronic liver disease non-alcoholic steatohepatitis (NASH). At 10 months of age, BDNF-heterozygous (BDNF +/- ) mice developed symptoms of NASH: centrilobular/perivenular steatosis, lobular inflammation with infiltration of neutrophils, ballooning hepatocytes, and fibrosis of the liver. Obesity and higher serum levels of glucose and insulin - major pathologic features in human NASH - were dramatic. Dying adipocytes were surrounded by macrophages in visceral fat, suggesting that chronic inflammation occurs in peripheral organs. RNA sequencing (RNA-seq) studies of the liver revealed that the most significantly enriched Gene Ontology term involved fatty acid metabolic processes and the modulation of neutrophil aggregation, pathologies that well characterise NASH. Gene expression analysis by RNA-seq also support the notion that BDNF +/- mice are under oxidative stress, as indicated by alterations in the expression of the cytochrome P450 family and a reduction in glutathione S-transferase p, an antioxidant enzyme. Histopathologic phenotypes of NASH were also observed in a knock-in mouse (BDNF +/pro ), in which the precursor BDNF is inefficiently converted into the mature form of BDNF. Lastly, as BDNF reduction causes overeating and subsequent obesity, a food restriction study was conducted in BDNF +/pro mice. Pair-fed BDNF +/pro mice developed hepatocellular damage and showed infiltration of inflammatory cells, including neutrophils in the liver, despite having body weights and blood parameters that were comparable to those of controls. This is the first report demonstrating that reduced BDNF expression plays a role in the pathogenic mechanism of NASH, which is a hepatic manifestation of metabolic syndrome. © 2023 The Pathological Society of Great Britain and Ireland.
Keyphrases
- oxidative stress
- high fat diet induced
- stress induced
- rna seq
- metabolic syndrome
- single cell
- weight gain
- insulin resistance
- growth factor
- type diabetes
- poor prognosis
- induced apoptosis
- adipose tissue
- fatty acid
- endothelial cells
- body mass index
- weight loss
- dna damage
- liver injury
- cell death
- preterm infants
- drug induced
- high fat diet
- gene expression
- long non coding rna
- radiation therapy
- neoadjuvant chemotherapy
- physical activity
- signaling pathway
- skeletal muscle
- blood pressure
- endoplasmic reticulum stress
- birth weight
- rectal cancer
- locally advanced
- cell cycle arrest