Hepatocytes reprogram liver macrophages involving control of TGF-beta activation, influencing liver regeneration and injury.

Abstract:

BACKGROUND: Macrophages play an important role in maintaining liver homeostasis and regeneration. However, it is not clear to what extent the different macrophage populations of the liver differ in terms of their activation state and which other liver cell populations may play a role in regulating the same. METHODS: Reverse transcription PCR, flow cytometry, transcriptome, proteome, secretome, single cell analysis, and immunohistochemical methods were used to study changes in gene expression as well as the activation state of macrophages in vitro and in vivo under homeostatic conditions and after partial hepatectomy. RESULTS: We show that F4/80+/CD11bhi/CD14hi macrophages of the liver are recruited in a C-C motif chemokine receptor (CCR2)-dependent manner and exhibit an activation state that differs substantially from that of the other liver macrophage populations, which can be distinguished on the basis of CD11b and CD14 expressions. Thereby, primary hepatocytes are capable of creating an environment in vitro that elicits the same specific activation state in bone marrow-derived macrophages as observed in F4/80+/CD11bhi/CD14hi liver macrophages in vivo. Subsequent analyses, including studies in mice with a myeloid cell-specific deletion of the TGF-beta type II receptor, suggest that the availability of activated TGF-beta and its downregulation by a hepatocyte-conditioned milieu are critical. Reduction of TGF-betaRII-mediated signal transduction in myeloid cells leads to upregulation of IL-6, IL-10, and SIGLEC1 expression, a hallmark of the activation state of F4/80+/CD11bhi/CD14hi macrophages, and enhances liver regeneration. CONCLUSIONS: The availability of activated TGF-beta determines the activation state of specific macrophage populations in the liver, and the observed rapid transient activation of TGF-beta may represent an important regulatory mechanism in the early phase of liver regeneration in this context.

SEEK ID: https://fairdomhub.org/publications/693

PubMed ID: 37486964

Projects: LiSyM Core Infrastructure and Management (LiSyM-PD)

Publication type: Journal

Journal: Hepatol Commun

Citation: Hepatol Commun. 2023 Jul 24;7(8):e0208. doi: 10.1097/HC9.0000000000000208. eCollection 2023 Aug 1.

Date Published: 1st Aug 2023

Registered Mode: by PubMed ID

Authors: S. D. Wolf, C. Ehlting, S. Muller-Dott, G. Poschmann, P. Petzsch, T. Lautwein, S. Wang, B. Helm, M. Schilling, J. Saez-Rodriguez, M. Vucur, K. Stuhler, K. Kohrer, F. Tacke, S. Dooley, U. Klingmuller, T. Luedde, J. G. Bode

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Created: 7th Mar 2024 at 12:17

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