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Stem cell therapy offers new hope for the treatment of Alzheimer's disease.

作者信息

He Guodong, Huang Jingnan, Zeng Zhaodi, Sun Huiyu, Wu Chao, Xu Qi, Hu Chuanchen, Jin Bei, Tong Minfeng, Wang Chengde

机构信息

Department of Neurosurgery, Affiliated Jinhua Hospital, Zhejiang University School of Medicine, Jinhua, Zhejiang, China.

Department of Neurosurgery, Wencheng Hospital Affiliated of Wenzhou Medical University, Wenzhou, Zhejiang, China.

出版信息

Front Cell Dev Biol. 2025 Aug 14;13:1650885. doi: 10.3389/fcell.2025.1650885. eCollection 2025.


DOI:10.3389/fcell.2025.1650885
PMID:40894925
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12391054/
Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder primarily characterized by memory impairment and cognitive decline, for which no curative treatment is currently available. Existing therapeutic strategies, such as cholinesterase inhibitors and N-methyl-D-aspartate (NMDA) receptor antagonists, can only provide limited symptomatic relief and fail to halt disease progression. In recent years, stem cell therapy has emerged as a promising approach for AD due to its multifaceted mechanisms of action. The therapeutic effects of stem cells in AD are mainly attributed to their ability to differentiate into functional neurons or glial cells, thereby replacing damaged cells and repairing neural networks. In addition, stem cells secrete neurotrophic and anti-inflammatory factors that contribute to the improvement of the brain microenvironment. Furthermore, they can regulate neuroinflammation, promote the clearance of β-amyloid (Aβ) deposits, and suppress neuroinflammation, thus potentially slowing disease progression. However, several challenges remain, including low cell survival rates, immune rejection, tumorigenic risks, and difficulties in crossing the blood-brain barrier. Looking ahead, the integration of advanced technologies such as organoid models, gene editing, artificial intelligence, and multi-omics approaches may drive substantial progress in the clinical translation of stem cell therapies for AD. Although still in its early stages, the future of this therapeutic strategy holds great promise.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/67516e316c98/fcell-13-1650885-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/2dba31661568/fcell-13-1650885-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/53f69b127a1b/fcell-13-1650885-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/c0b9c41ead72/fcell-13-1650885-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/67516e316c98/fcell-13-1650885-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/2dba31661568/fcell-13-1650885-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/53f69b127a1b/fcell-13-1650885-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/c0b9c41ead72/fcell-13-1650885-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe26/12391054/67516e316c98/fcell-13-1650885-g004.jpg

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本文引用的文献

[1]
Progress of bone marrow mesenchymal stem cell transplantation on neural plasticity in brain.

Front Cell Dev Biol. 2025-6-10

[2]
Astrocyte induction of disease-associated microglia is suppressed by acute exposure to fAD neurons in human iPSC triple cultures.

Cell Rep. 2025-6-24

[3]
Alzheimer's disease pathogenesis: standing at the crossroad of lipid metabolism and immune response.

Mol Neurodegener. 2025-6-4

[4]
Examining the association between synaptic density and neurofibrillary tau among cognitively impaired and unimpaired older adults with and without Alzheimer's disease pathology.

Alzheimers Dement. 2025-6

[5]
Progression of differentiation of iPSCs into specific subtypes of neurons.

Differentiation. 2025

[6]
Amyloid β-Induced Inflammarafts in Alzheimer's Disease.

Int J Mol Sci. 2025-5-10

[7]
Stem cell therapy: a revolutionary cure or a pandora's box.

Stem Cell Res Ther. 2025-5-22

[8]
Biological Effects of Dietary Restriction on Alzheimer's Disease: Experimental and Clinical Investigations.

CNS Neurosci Ther. 2025-4

[9]
Physical activity in Alzheimer's disease prevention: Sex differences and the roles of BDNF and irisin.

Front Neuroendocrinol. 2025-4

[10]
Maximizing the benefit and managing the risk of anti-amyloid monoclonal antibody therapy for Alzheimer's disease: Strategies and research directions.

Neurotherapeutics. 2025-4

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