Evidence map›Paper›PMID 41390791›Full record

ArticleScientific reports2025

Splenectomy reduces shear stress and inflammation in liver endothelial cells during regeneration after partial hepatectomy in mice.

Andrey Elchaninov, Elena Gantsova, Polina Vishnyakova, Maria Kuznetsova, Dmitry Trofimov, Timur Fatkhudinov, Gennady Sukhikh

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

7 authors.

Andrey ElchaninovLaboratory of Growth and Development, Avtsyn Research Institute of Human Morphology of FSBI "Petrovsky National Research Centre of Surgery", 3 Tsuruppa Street, Moscow, 117418, Russia. elchandrey@yandex.ru.
Elena GantsovaLaboratory of Growth and Development, Avtsyn Research Institute of Human Morphology of FSBI "Petrovsky National Research Centre of Surgery", 3 Tsuruppa Street, Moscow, 117418, Russia.
Polina VishnyakovaLaboratory of Regenerative Medicine, Institute of Translational Medicine, Gynecology and Perinatology Named After Academician V.I., National Medical Research Centre for Obstetrics, Kulakov of Ministry of Healthcare of Russian Federation, Moscow, Russia.
Maria KuznetsovaLaboratory of Molecular Research Methods, Institute of Reproductive Genetics, National Medical Research Centre for Obstetrics, Gynecology and Perinatology Named After Academician V.I., Kulakov of Ministry of Healthcare of Russian Federation, Moscow, Russia.
Dmitry TrofimovLaboratory of Molecular Research Methods, Institute of Reproductive Genetics, National Medical Research Centre for Obstetrics, Gynecology and Perinatology Named After Academician V.I., Kulakov of Ministry of Healthcare of Russian Federation, Moscow, Russia.
Timur FatkhudinovLaboratory of Growth and Development, Avtsyn Research Institute of Human Morphology of FSBI "Petrovsky National Research Centre of Surgery", 3 Tsuruppa Street, Moscow, 117418, Russia.
Gennady SukhikhLaboratory of Regenerative Medicine, Institute of Translational Medicine, Gynecology and Perinatology Named After Academician V.I., National Medical Research Centre for Obstetrics, Kulakov of Ministry of Healthcare of Russian Federation, Moscow, Russia.

Funding

Russian Science Foundation 22-14-00152-P
6 · The paper itself

Abstract

Clinical and experimental findings indicate that splenectomy stimulates liver regeneration. The mechanisms of this effect are uncertain. This study aimed to assess the effect of splenectomy on the state of sinusoidal endothelial cells during liver regeneration after 70% resection in mouse model. Two series of experiments were performed. In the first series, splenectomy was performed on sexually mature male C57BL/6 mice, followed by 70% liver resection 7 days later. In the second series, only 70% liver resection was performed. The animals were withdrawn from the experiment 1, 3, or 7 days post-resection. The measurements encompassed the liver mass recovery dynamics; the AST, ALT, and albumin levels; and the proliferation activity of hepatocytes, as well as gene expression profiles, apoptosis rates, and proliferation activity of liver sinusoidal endothelial cells. Animals that underwent splenectomy before liver resection showed a decrease in the number of endothelial cells positive for VCAM-1 on days 1 and 7 post-resection and VE-cadherin-positive (CD144 +) cells on day 7. Liver resection caused an increase in the relative counts of dying (Annexin-PI +) and Ki67 + endothelial cells in the remnant. The apoptotic endothelial cell counts were significantly higher in the group with preserved spleen on day 1 post-resection, while the number of Ki67 + endotheliocytes was higher in splenectomized animals on day 1 and day 3 post-resection. Splenectomy exerts significant effect on the state of endothelial cells of the sinusoidal capillaries of the regenerating liver. The gene expression profiling studied by microarray technology using Clariom™ S Assay (mouse) revealed specific enrichment of the following signaling pathways in the endothelial cells of regenerating liver in splenectomized animals: PI3K-Akt-mTOR signaling pathway, Focal adhesion pathway, Chemokine signaling pathway. In this case, most of the differentially expressed genes were repressed. The decreased proinflammatory activation of sinusoidal endothelium results in decreased immigration of lymphocytes, notably CD3 + и NK1.1 lymphocytes known to inhibit the regeneration. The results indicate that prior splenectomy mitigates the manifestation of shear stress in endothelial cells of the liver and reduces their pro-inflammatory activation, resulting in lower rates of migration of regeneration-inhibiting lymphocytes to the regenerating liver.

Indexed as

Endothelial CellsHepatectomyInflammationLiverLiver RegenerationSplenectomyAnimalsApoptosisCell ProliferationHepatocytesMaleMiceMice, Inbred C57BLStress, MechanicalEndothelial cellsLiverRegenerationSpleen

Identifiers

PMID41390791
PMCPMC12824239

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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.