Frontiers in Molecular Biosciences (Aug 2023)

Cellular heterogeneity and plasticity during NAFLD progression

  • Hyun-Ju Park,
  • Hyun-Ju Park,
  • Juyong Choi,
  • Juyong Choi,
  • Hyunmi Kim,
  • Hyunmi Kim,
  • Da-Yeon Yang,
  • Da-Yeon Yang,
  • Tae Hyeon An,
  • Tae Hyeon An,
  • Eun-Woo Lee,
  • Eun-Woo Lee,
  • Baek-Soo Han,
  • Baek-Soo Han,
  • Sang Chul Lee,
  • Sang Chul Lee,
  • Won Kon Kim,
  • Won Kon Kim,
  • Kwang-Hee Bae,
  • Kwang-Hee Bae,
  • Kyoung-Jin Oh,
  • Kyoung-Jin Oh

DOI
https://doi.org/10.3389/fmolb.2023.1221669
Journal volume & issue
Vol. 10

Abstract

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Nonalcoholic fatty liver disease (NAFLD) is a progressive liver disease that can progress to nonalcoholic steatohepatitis (NASH), NASH-related cirrhosis, and hepatocellular carcinoma (HCC). NAFLD ranges from simple steatosis (or nonalcoholic fatty liver [NAFL]) to NASH as a progressive form of NAFL, which is characterized by steatosis, lobular inflammation, and hepatocellular ballooning with or without fibrosis. Because of the complex pathophysiological mechanism and the heterogeneity of NAFLD, including its wide spectrum of clinical and histological characteristics, no specific therapeutic drugs have been approved for NAFLD. The heterogeneity of NAFLD is closely associated with cellular plasticity, which describes the ability of cells to acquire new identities or change their phenotypes in response to environmental stimuli. The liver consists of parenchymal cells including hepatocytes and cholangiocytes and nonparenchymal cells including Kupffer cells, hepatic stellate cells, and endothelial cells, all of which have specialized functions. This heterogeneous cell population has cellular plasticity to adapt to environmental changes. During NAFLD progression, these cells can exert diverse and complex responses at multiple levels following exposure to a variety of stimuli, including fatty acids, inflammation, and oxidative stress. Therefore, this review provides insights into NAFLD heterogeneity by addressing the cellular plasticity and metabolic adaptation of hepatocytes, cholangiocytes, hepatic stellate cells, and Kupffer cells during NAFLD progression.

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