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Neural progenitor cells derived from fibroblasts induced by small molecule compounds under hypoxia for treatment of Parkinson's disease in rats

文献类型： 外文期刊

作者： Guo, Yu 1 ; Wang, Yuan-Yuan 1 ; Sun, Ting-Ting 1 ; Xu, Jia-Jia 1 ; Yang, Pan 1 ; Ma, Cai-Yun 1 ; Guan, Wei-Jun 2 ; Wang, Chun-Jing 1 ; Liu, Gao-Feng 1 ; Liu, Chang-Qing 1 ;

作者机构： 1.Bengbu Med Coll, Sch Lab Med, Sch Life Sci, Bengbu, Anhui, Peoples R China

2.Chinese Acad Agr Sci, Inst Anim Sci, Natl Germplasm Resource Ctr Domest Anim, Beijing, Peoples R China

3.Univ Connecticut, Hlth Ctr, Dept Neurosci, Farmington, CT 06030 USA

关键词： cell reprogramming; cell transplantation; hypoxia; neural progenitor cells; neurological function; Parkinson's disease; small molecule compounds; substantia nigra

期刊名称：NEURAL REGENERATION RESEARCH （ 影响因子：6.1； 五年影响因子：5.1 ）

ISSN： 1673-5374

年卷期： 2023 年 18 卷 5 期

页码：

收录情况： SCI

摘要： Neural progenitor cells (NPCs) capable of self-renewal and differentiation into neural cell lineages offer broad prospects for cell therapy for neurodegenerative diseases. However, cell therapy based on NPC transplantation is limited by the inability to acquire sufficient quantities of NPCs. Previous studies have found that a chemical cocktail of valproic acid, CHIR99021, and Repsox (VCR) promotes mouse fibroblasts to differentiate into NPCs under hypoxic conditions. Therefore, we used VCR (0.5 mM valproic acid, 3 mu M CHIR99021, and 1 mu M Repsox) to induce the reprogramming of rat embryonic fibroblasts into NPCs under a hypoxic condition (5%). These NPCs exhibited typical neurosphere-like structures that can express NPC markers, such as Nestin, SRY-box transcription factor 2, and paired box 6 (Pax6), and could also differentiate into multiple types of functional neurons and astrocytes in vitro. They had similar gene expression profiles to those of rat brain-derived neural stem cells. Subsequently, the chemically-induced NPCs (ciNPCs) were stereotactically transplanted into the substantia nigra of 6-hydroxydopamine-lesioned parkinsonian rats. We found that the ciNPCs exhibited long-term survival, migrated long distances, and differentiated into multiple types of functional neurons and glial cells in vivo. Moreover, the parkinsonian behavioral defects of the parkinsonian model rats grafted with ciNPCs showed remarkable functional recovery. These findings suggest that rat fibroblasts can be directly transformed into NPCs using a chemical cocktail of VCR without introducing exogenous factors, which may be an attractive donor material for transplantation therapy for Parkinson's disease.

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