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Intraocular liver spheroids for non-invasive high-resolution in vivo monitoring of liver cell function.


ABSTRACT: Longitudinal monitoring of liver function in vivo is hindered by the lack of high-resolution non-invasive imaging techniques. Using the anterior chamber of the mouse eye as a transplantation site, we have established a platform for longitudinal in vivo imaging of liver spheroids at cellular resolution. Transplanted liver spheroids engraft on the iris, become vascularized and innervated, retain hepatocyte-specific and liver-like features and can be studied by in vivo confocal microscopy. Employing fluorescent probes administered intravenously or spheroids formed from reporter mice, we showcase the potential use of this platform for monitoring hepatocyte cell cycle activity, bile secretion and lipoprotein uptake. Moreover, we show that hepatic lipid accumulation during diet-induced hepatosteatosis is mirrored in intraocular in vivo grafts. Here, we show a new technology which provides a crucial and unique tool to study liver physiology and disease progression in pre-clinical and basic research.

SUBMITTER: Lazzeri-Barcelo F 

PROVIDER: S-EPMC10817975 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature

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Intraocular liver spheroids for non-invasive high-resolution in vivo monitoring of liver cell function.

Lazzeri-Barcelo Francesca F   Oliva-Vilarnau Nuria N   Baniol Marion M   Leibiger Barbara B   Bergmann Olaf O   Lauschke Volker M VM   Leibiger Ingo B IB   Moruzzi Noah N   Berggren Per-Olof PO  

Nature communications 20240126 1


Longitudinal monitoring of liver function in vivo is hindered by the lack of high-resolution non-invasive imaging techniques. Using the anterior chamber of the mouse eye as a transplantation site, we have established a platform for longitudinal in vivo imaging of liver spheroids at cellular resolution. Transplanted liver spheroids engraft on the iris, become vascularized and innervated, retain hepatocyte-specific and liver-like features and can be studied by in vivo confocal microscopy. Employin  ...[more]

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