The neuroprotective effect of rat adipose tissue-derived mesenchymal stem cell-conditioned medium on cortical neurons using an in vitro model of SCI inflammation

被引:14
|
作者
Szekiova, Eva [1 ]
Slovinska, Lucia [1 ]
Blasko, Juraj [1 ]
Plsikova, Jana [2 ,3 ]
Cizkova, Dasa [4 ,5 ]
机构
[1] Slovak Acad Sci, Inst Neurobiol, Kosice, Slovakia
[2] Safarik Univ, Fac Med, Associated Tissue Bank, Kosice, Slovakia
[3] L Pasteur Univ Hosp, Kosice, Slovakia
[4] Slovak Acad Sci, Inst Neuroimmunol, Bratislava, Slovakia
[5] Univ Vet Med & Pharm Kosice, Dept Ananat Histol & Physiol, Kosice, Slovakia
关键词
Mesenchymal stem cells; neurons; conditioned medium; neuroprotection; BONE-MARROW; STROMAL CELLS; GLUTAMATE EXCITOTOXICITY; DIFFERENTIATION; SECRETOME; BRAIN; PROLIFERATION; TIME;
D O I
10.1080/01616412.2018.1432266
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: In this study, anew approach was used with an in vitro model in which neural cells were exposed to conditioned media from the injured spinal cord (SCI-CM) mimicking a local inflammatory microenvironment . Subsequently, the neuroprotective effect of rat adipose tissue-derived msesenchymal stem cell-conditioned media (ATMSC-CM) was investigated through a cell-free based therapy, which was used to treat cortical neurons and astrocytes under inflammation. Methods: Primary cell cultures isolated from postnatal day (P6) Wistar rat brain cortex were exposed to SCI-CM derived from the central lesion, rostral and caudal segments of injured spinal cord. After 48h incubation, the SCI-CM was replaced and primary cultures were cultivated either in DMEM media alone or in ATMSC-CM for 72h. The impact of ATMSC-CM on the viability of neurons and astrocytes was assessed using a CyQUANT (R) Direct Cell Proliferation Assay Kit as well as immunocytochemistry analysis. Results: Immunocytochemical analysis revealed significant decrease in the number of MAP2 positive neurons exposed to SCI-CM compared to Control. Protection by ATMSC-CM was associated with increased survival of neurons compared to primary culture cultivated in DMEM media alone. The ATMSC-CM effect on astrocytes was more variable and without any significant impact. Conclusion: The results demonstrate that SCI-CM mimicking inflammation can reduce cortical neuron survival, and subsequent exposure to ATMSC-CM can stabilize the neuronal population most likely via released neuroprotective and trophic factors. In addition, astrogliosis was not affected by ATMSC-CM.
引用
收藏
页码:258 / 267
页数:10
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