Evidence map›Paper›PMID 41805789›Full record

ArticleJCI insight2026

Loss of fungal sensing exacerbates liver injury in a murine model of MASLD.

Vijay Pandyarajan, So Yeon Kim, Takashi Tsuchiya, Selena Liu, Sadam H Bhat, Jieun Kim, David M Underhill, Mazen Noureddin, Shelly C Lu, Ekihiro Seki

Abstract read
In one paragraph

Article in JCI insight, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Vijay PandyarajanKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
So Yeon KimKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
Takashi TsuchiyaKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
Selena LiuKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
Sadam H BhatKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
Jieun KimKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
David M UnderhillKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
Mazen NoureddinKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
Shelly C LuKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.
Ekihiro SekiKarsh Division of Gastroenterology and Hepatology, Department of Medicine, and.

Funding

LPS binding to TLR4 regulates hepatic stellate cell activation and fibrosisR01DK085252 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI EKIHIRO SEKI · 2011 to 2026
$4.8M
Determination of Molecular Mechanism of Stellate Cell-Mediated FibrosisR01DK138591 · NIDDK · CEDARS-SINAI MEDICAL CENTER · PI EKIHIRO SEKI · 2024 to 2026
$1.7M
NIDDK NIH HHS R01 DK085252NIDDK NIH HHS R01 DK138591
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a global health concern with limited interventions. While the role of gut bacteria in MASLD has been extensively studied, the contribution of gut fungi remains largely unexplored. This study investigates the impact of fungal dysbiosis and the role of CARD9, a key adaptor protein in fungal sensing on gut-liver axis dysfunction in MASLD. Patients with advanced liver fibrosis exhibited distinct mycobiota profiles. Using a Card9-deficient mouse model subjected to high-fat, high-glucose/-fructose feeding, we observed exacerbated liver injury and fibrosis accompanied by fungal dysbiosis, paralleling our findings in human patients. Beyond its established expression in myeloid cells, CARD9 was also detected in intestinal enterocytes where its expression was diminished under metabolic stress. Intestinal organoids with CARD9 inhibition had reduced expression of antimicrobial Reg3g, the tight junction protein ZO-1, and the antifungal enteroendocrine hormone PYY. These findings suggest that CARD9 maintains gut barrier integrity, preventing microbial translocation and subsequent liver injury and fibrosis. Our results provide insights into the interplay between fungal dysbiosis, gut barrier dysfunction, and MASLD, and identify CARD9 as a key protein within this axis.

Indexed as

CARD Signaling Adaptor ProteinsDysbiosisAnimalsDisease Models, AnimalGastrointestinal MicrobiomeHumansIntestinal Barrier FunctionLiverLiver CirrhosisMaleMiceMice, Inbred C57BLMice, KnockoutPancreatitis-Associated ProteinsZonula Occludens-1 ProteinCARD9 protein, humanCard9 protein, mouseCARD Signaling Adaptor ProteinsPancreatitis-Associated ProteinsReg3g protein, mouseTjp1 protein, mouseZonula Occludens-1 ProteinGastroenterologyHepatitisHepatologyObesity

Identifiers

PMID41805789
PMCPMC13135407

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.