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载胶质细胞源性神经营养因子的水凝胶微载体增强帕金森病大鼠模型中多巴胺能神经元的植入。

Cryogel microcarriers loaded with glial cell line-derived neurotrophic factor enhance the engraftment of primary dopaminergic neurons in a rat model of Parkinson's disease.

机构信息

Pharmacology & Therapeutics and Galway Neuroscience Centre, University of Galway, Galway, Ireland.

School of Pharmacy and Pharmaceutical Sciences, Cardiff University, King Edward VII Avenue, Cardiff, United Kingdom.

出版信息

J Neural Eng. 2024 Sep 12;21(5). doi: 10.1088/1741-2552/ad7761.

Abstract

Cryogel microcarriers made of poly(ethylene glycol) diacrylate and 3-sulfopropyl acrylate have the potential to act as delivery vehicles for long-term retention of neurotrophic factors (NTFs) in the brain. In addition, they can potentially enhance stem cell-derived dopaminergic (DAergic) cell replacement strategies for Parkinson's disease (PD), by addressing the limitations of variable survival and poor differentiation of the transplanted precursors due to neurotrophic deprivation post-transplantation in the brain. In this context, to develop a proof-of-concept, the aim of this study was to determine the efficacy of glial cell line-derived NTF (GDNF)-loaded cryogel microcarriers by assessing their impact on the survival of, and reinnervation by, primary DAergic grafts after intra-striatal delivery in Parkinsonian rat brains.Rat embryonic day 14 ventral midbrain cells were transplanted into the 6-hydroxydopamine-lesioned striatum either alone, or with GDNF, or with unloaded cryogel microcarriers, or with GDNF-loaded cryogel microcarriers., GDNF and tyrosine hydroxylase immunostaining were used to identify retention of the delivered GDNF within the implanted cryogel microcarriers, and to identify the transplanted DAergic neuronal cell bodies and fibres in the brains, respectively.We found an intact presence of GDNF-stained cryogel microcarriers in graft sites, indicating their ability for long-term retention of the delivered GDNF up to 4 weeks in the brain. This resulted in an enhanced survival (1.9-fold) of, and striatal reinnervation (density & volume) by, the grafted DAergic neurons, in addition to an enhanced sprouting of fibres within graft sites.This data provides an important proof-of-principle for the beneficial effects of neurotrophin-loaded cryogel microcarriers on engraftment of cells in the context of cell replacement therapy in PD. For clinical translation, further studies will be needed to assess the impact of cryogel microcarriers on the survival and differentiation of stem cell-derived DAergic precursors in Parkinsonian rat brains.

摘要

聚乙二醇二丙烯酸酯和 3-磺丙基丙烯酸钠制成的水凝胶微载体有可能作为神经营养因子(NTFs)在大脑中的长期保留的递送载体。此外,它们还可以通过解决移植后由于神经营养剥夺导致移植前体细胞的存活和分化不良的问题,增强用于帕金森病(PD)的干细胞衍生多巴胺能(DAergic)细胞替代策略。在这种情况下,为了开发概念验证,本研究的目的是通过评估胶质细胞衍生神经营养因子(GDNF)负载的水凝胶微载体对帕金森大鼠脑内纹状体移植后原发性 DAergic 移植物的存活和再神经支配的影响来确定其疗效。将大鼠胚胎 14 天的中脑神经细胞单独或与 GDNF 一起或与未加载的水凝胶微载体一起或与 GDNF 加载的水凝胶微载体一起移植到 6-羟多巴胺损伤的纹状体中。使用 GDNF 和酪氨酸羟化酶免疫染色来鉴定递送到植入水凝胶微载体中的 GDNF 的保留情况,以及分别鉴定大脑中移植的 DAergic 神经元细胞体和纤维。我们发现 GDNF 染色的水凝胶微载体在移植物部位完整存在,表明其能够在大脑中长时间保留递送到的 GDNF,最长可达 4 周。这导致移植的 DAergic 神经元的存活(增加 1.9 倍)和纹状体再神经支配(密度和体积)增强,以及移植物部位内纤维的增强发芽。这些数据为神经生长因子负载的水凝胶微载体在 PD 细胞替代治疗中对细胞移植的有益作用提供了重要的原理证明。为了临床转化,需要进一步研究来评估水凝胶微载体对帕金森大鼠脑内干细胞衍生 DAergic 前体细胞的存活和分化的影响。

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