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Inflammatory Cytokine TNFα Promotes the Long-Term Expansion of Primary Hepatocytes in 3D Culture
Author(s) -
Weng Chuan Peng,
Catriona Y. Logan,
Matt Fish,
Teni Anbarchian,
Francis Aguisanda,
Adrián Álvarez-Varela,
Peng Wu,
Yinhua Jin,
Junjie Zhu,
Bin Li,
Markus Grompe,
Bruce Wang,
Roel Nusse
Publication year - 2018
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2018.11.012
Subject(s) - biology , hepatocyte , microbiology and biotechnology , wnt signaling pathway , cytokine , in vitro , tumor necrosis factor alpha , cell culture , extracellular , bile duct , immunology , signal transduction , medicine , genetics
In the healthy adult liver, most hepatocytes proliferate minimally. However, upon physical or chemical injury to the liver, hepatocytes proliferate extensively in vivo under the direction of multiple extracellular cues, including Wnt and pro-inflammatory signals. Currently, liver organoids can be generated readily in vitro from bile-duct epithelial cells, but not hepatocytes. Here, we show that TNFα, an injury-induced inflammatory cytokine, promotes the expansion of hepatocytes in 3D culture and enables serial passaging and long-term culture for more than 6 months. Single-cell RNA sequencing reveals broad expression of hepatocyte markers. Strikingly, in vitro-expanded hepatocytes engrafted, and significantly repopulated, the injured livers of Fah -/- mice. We anticipate that tissue repair signals can be harnessed to promote the expansion of otherwise hard-to-culture cell-types, with broad implications.

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