Evidence map›Paper›PMID 42552328›Full record

ArticleScientific reports2026

Transcriptomic profiling of HBV transgenic mouse livers reveals ZBP1-associated necroptotic signaling.

Zean Wang, Mengyuan Zhao, Yun Fu, Lili Liu, Yong Hou, Mei Shi, Fei Gao, Guoliang Zhang

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Zean Wang *First Clinical Medical College, Anhui University of Chinese Medicine, Hefei, China.
Mengyuan Zhao *Hefei Preschool Education College, Hefei, China.
Yun Fu *First Clinical Medical College, Anhui University of Chinese Medicine, Hefei, China.
Lili LiuDepartment of Infectious Disease, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, China.
Yong HouDepartment of Infectious Disease, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, China.
Mei ShiDepartment of Infectious Disease, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, China.
Fei GaoFirst Clinical Medical College, Anhui University of Chinese Medicine, Hefei, China.
Guoliang ZhangDepartment of Infectious Disease, The First Affiliated Hospital of Anhui University of Chinese Medicine, Hefei, China. zhangguoliang61@sina.com.

Funding

National Natural Science Foundation of China 81874451Xu Jingshi National TCM Master Studio Wan Mi 2023-11
6 · The paper itself

Abstract

Although transcriptome studies have been performed in cell culture models of HBV infection, the in vivo hepatic transcriptional response to persistent HBV expression remains incompletely characterized. In addition, whether HBV is associated with activation of necroptotic signaling in the liver has not been fully clarified. Therefore, this study aimed to: (1) define transcriptomic alterations in livers from an HBV transgenic mouse model; and (2) explore whether ZBP1-associated necroptotic signaling is present in HBV-Tg livers by integrating RNA-seq, bioinformatic analysis, and biochemical validation. We utilized an HBV transgenic mouse model and characterized it by measuring serum HBV DNA, HBsAg, AST, ALT, and TBIL levels and by performing hematoxylin and eosin (H&E) staining. Subsequently, the expression of protein-coding genes in HBV transgenic and control mice was analyzed by next-generation RNA sequencing (RNA-seq). Differentially expressed genes (DEGs) were identified using EdgeR with thresholds of |log2(fold change)| > 1 and P value < 0.05. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses were performed on the DEGs. A protein-protein interaction (PPI) network was constructed based on the STRING database, and PPI modules were analyzed using the MCODE plugin in Cytoscape. Finally, we evaluated ZBP1-associated necroptotic signaling by examining the protein levels of ZBP1 and phosphorylated RIPK3/MLKL by Western blot. We identified 815 candidate differentially expressed genes, including 412 upregulated and 403 downregulated genes in HBV-Tg livers compared with control livers. KEGG pathway analysis indicated enrichment of immune-related pathways, metabolic pathways, and viral infection-related pathways. Zbp1 drew further attention because it was increased in HBV-Tg livers and located within an interferon/innate immune-related PPI module. At the protein level, ZBP1, p-RIPK3, and p-MLKL were increased in HBV-Tg livers. These findings suggest elevated ZBP1-associated necroptosis-related markers in the HBV-Tg liver model. We profiled gene expression in livers from HBV-Tg and control mice using RNA-seq and identified candidate DEGs, GO terms, and pathway terms associated with HBV-related liver responses. Our data support an association between HBV-Tg liver status and increased ZBP1, p-RIPK3, and p-MLKL expression. However, additional functional studies are required to determine cell specificity, causal direction, and the contribution of this signaling axis to liver injury.

Indexed as

Hepatitis BHepatitis B virusLiverNecroptosisRNA-Binding ProteinsSignal TransductionTranscriptomeAnimalsGene Expression ProfilingMaleMiceMice, TransgenicProtein Interaction MapsRNA-Binding ProteinsZbp1 protein, mouseHBV transgenic micenecroptosisRNA-seqtranscriptomeZBP1

Identifiers

PMID42552328
PMCPMC13439201

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.