Hepatic stellate cell heterogeneity: Functional aspects and therapeutic implications

Hepatic stellate cells (HSCs) represent a highly heterogeneous mesenchymal cell population with multifaceted roles in liver homeostasis and disease. Beyond their well-established roles in vitamin A storage and scar formation, there is increasing evidence for HSCs in the regulation of hepatic metabolism, regeneration, immunity, and carcinogenesis. Here, we will review the heterogeneity of HSCs in the healthy, aging, and diseased liver, focusing on cell-cell interactions and their contributions to fibrosis, liver zonation and function, regeneration, and cancer. We explore the spatiotemporal diversity of HSCs, highlighting their subpopulations and their specialized roles, as well as the complex bidirectional communications between HSCs, hepatocytes, endothelial cells (ECs), macrophages/monocytes, T cells, and tumor cells. By integrating insights from single-cell sequencing, spatial transcriptomics, preclinical data, and clinical data, this review aims to provide an updated understanding of how HSC heterogeneity contributes to liver homeostasis and disease and can be targeted for therapeutic purposes.

Authors

Institutions

Publication Details

Journal
Hepatology
Published
2025-05-08
DOI
https://doi.org/10.1097/hep.0000000000001386
Citations
10
Primary Topic
Liver physiology and pathology
Type
article
Field-Weighted Citation Impact
13.22
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Hepatic stellate cell heterogeneity: Functional aspects and therapeutic implications

Robert F. Schwabe, Yana Geng
10 citations
Hepatology
Liver physiology and pathology
13.22
article

Hepatic stellate cell heterogeneity: Functional aspects and therapeutic implications

Robert F. Schwabe, Yana Geng
article en
10 citations

Abstract

Hepatic stellate cells (HSCs) represent a highly heterogeneous mesenchymal cell population with multifaceted roles in liver homeostasis and disease. Beyond their well-established roles in vitamin A storage and scar formation, there is increasing evidence for HSCs in the regulation of hepatic metabolism, regeneration, immunity, and carcinogenesis. Here, we will review the heterogeneity of HSCs in the healthy, aging, and diseased liver, focusing on cell-cell interactions and their contributions to fibrosis, liver zonation and function, regeneration, and cancer. We explore the spatiotemporal diversity of HSCs, highlighting their subpopulations and their specialized roles, as well as the complex bidirectional communications between HSCs, hepatocytes, endothelial cells (ECs), macrophages/monocytes, T cells, and tumor cells. By integrating insights from single-cell sequencing, spatial transcriptomics, preclinical data, and clinical data, this review aims to provide an updated understanding of how HSC heterogeneity contributes to liver homeostasis and disease and can be targeted for therapeutic purposes.

Hepatology
Columbia University Irving Medical Center (US), Center for Digestive and Liver Diseases (US), Human Longevity (United States) (US), Columbia University (US)
Good health and well-being
Openalex Percentile: Top 1%
Liver physiology and pathology
13.22
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.