Evidence map›Paper›PMID 42888005›Full record

ArticleStem cells translational medicine2026

Human umbilical cord mesenchymal stem cells alleviate brain injury and promote neuroregeneration via BDNF/TrkB/CREB/PI3K-Akt pathway in preterm rats with intraventricular hemorrhage.

Mingyou Yu, Ziyi Zhang, Xuxian Wu, Baoying Zhang, Yang Hu, Changge Wei, Miao Ran, Manni Cao, Jinhui Zhang, Xueli Ding and 4 more

Abstract read
In one paragraph

Article in Stem cells translational medicine, 2026. 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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1 · What the graph read from it

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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

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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

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0 citing papers in PubMed.

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4 · The record

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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

14 authors.

Mingyou YuCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Ziyi ZhangCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Xuxian WuCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.ORCID 0009-0006-7565-2486
Baoying ZhangCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Yang HuCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Changge WeiCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Miao RanCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Manni CaoCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Jinhui ZhangCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Xueli DingCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Yan WangCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.
Can LiuGuizhou Guizhong Biotechnology Co., Ltd., Guiyang 550000, Guizhou, China.
Maoqiong ChenDepartment of Neonatology, Affiliated Hospital of Guizhou Medical University, Guiyang 550000, Guizhou, China.
Jianwei XuCenter for Tissue Engineering and Stem Cell Research, Guizhou Medical University, Guiyang 550000, Guizhou, China.

Funding

Joint Project of Guizhou Medical University and Guizhong Biotechnology Co., Ltd HY2402National Natural Science Foundation of China 82160126Science and Technology Fund of Guizhou Provincial Health Commission gzwkj2023-093Science and Technology Fund of Guizhou Provincial Health Commission gzwkj2026-062
6 · The paper itself

Abstract

objectiveTo explore the neuroprotective effect and molecular mechanism of human umbilical cord mesenchymal stem cells (hUC-MSCs) in preterm rats with intraventricular hemorrhage (IVH), and provide experimental basis for clinical treatment of neonatal IVH.

methodsTissue block adherence method was used to isolate and culture hUC-MSCs, and P4 Sprague-Dawley premature rats were divided into sham, IVH model, and hUC-MSC treatment groups. Collagenase VIIS was injected to establish IVH model, and hUC-MSCs were injected into lateral ventricles. Cell colonization, body weight, neurobehavior, brain histology, apoptosis, and related molecular indicators were detected via fluorescence tracking, behavioral tests, staining, RT-PCR, Western blot (WB), and ELISA. Bioinformatics combined with ANA12 blocking assay verified core pathways.

resultshUC-MSCs survived in rat brain for at least 7 days. Compared with the model group, the treatment group gained weight faster, neurobehavioral function was markedly improved, neuronal apoptosis decreased sharply, and brain tissue damage was alleviated. hUC-MSCs up-regulated anti-apoptotic, anti-inflammatory, antioxidant and neurogenesis-related molecules and activated BDNF/TrkB/CREB/PI3K-Akt pathway; TrkB blockade reversed all protective effects.

conclusionhUC-MSCs exert multi-target neuroprotection by activating BDNF/TrkB/CREB/PI3K-Akt pathway, which offers a novel strategy for IVH treatment in preterm infants.

Indexed as

Brain InjuriesCerebral HemorrhageCerebral Intraventricular HemorrhageMesenchymal Stem CellsMesenchymal Stem Cell TransplantationNerve RegenerationUmbilical CordAnimalsAnimals, NewbornApoptosisBrain-Derived Neurotrophic FactorCyclic AMP Response Element-Binding ProteinDisease Models, AnimalFemaleHumansMaleBrain-Derived Neurotrophic FactorCyclic AMP Response Element-Binding ProteinPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor, trkBhuman umbilical cord-derived mesenchymal stem cellsintraventricular hemorrhageneuroprotectionpreterm ratssignaling pathway

Identifiers

PMID42888005
PMCPMC13675110

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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.