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Conditioned Medium Protects Dopaminergic Neurons in Parkinsonian Rats
OBJECTIVE: Adipose derived stem cells (ASCs) secrete numerous neurotrophic factors and cytokines in conditioned medium (CM), which protect neurons by its antioxidative and trophic effects. This research assesses the neuroprotective effect of ASC- CM on neurotrophins genes expressions and tyrosine hy...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royan Institute
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004993/ https://www.ncbi.nlm.nih.gov/pubmed/29845788 http://dx.doi.org/10.22074/cellj.2018.5343 |
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author | Nakhaeifard, Malihe Haji Ghasem Kashani, Maryam Goudarzi, Iran Rezaei, Arezou |
author_facet | Nakhaeifard, Malihe Haji Ghasem Kashani, Maryam Goudarzi, Iran Rezaei, Arezou |
author_sort | Nakhaeifard, Malihe |
collection | PubMed |
description | OBJECTIVE: Adipose derived stem cells (ASCs) secrete numerous neurotrophic factors and cytokines in conditioned medium (CM), which protect neurons by its antioxidative and trophic effects. This research assesses the neuroprotective effect of ASC- CM on neurotrophins genes expressions and tyrosine hydroxylase positive (TH+) cell density in male Wistar rats lesioned by 6-hydroxydopamine (6-OHDA). MATERIALS AND METHODS: In this experimental study, the groups consisted of lesioned and sham rats with unilateral injections of 20 µg of 6-OHDA neurotoxin and phosphate buffered saline (PBS) into the striatum, respectively. Another groups received intravenous injections of 3×10(6) cells (ASCs group), 500 µl of CM (ASC-CM group) or medium [α-minimal essential medium (α-MEM) group)]. All rats underwent evaluations with the rotarod and apomorphine-induced rotation tests at 2, 4, 6, and 8 weeks post-injection. At 8 weeks we sacrificed some of the animals for real-time polymerase chain reaction (PCR) analysis, and evaluation of TH+cell counts. RESULTS: We observed a significant decrease in contralateral turns to the lesions in the ASCs and ASC-CM groups compared to the neurotoxin lesioned or α-MEM groups at 8 weeks post transplantation. Cell and CM- injected rats showed a significant increase of staying on the rotarod compared to the lesion or α-MEM groups. Cell and CM-treated rats showed significant increases in the NGF and NT3 genes, respectively, compared with the lesion group. Both treated groups showed significant increases in BDNF gene expression and TH(+) cell density. CONCLUSION: The results suggested that ASCs and ASC-CM protected dopaminergic neurons through the expressions of neurotrophin genes. |
format | Online Article Text |
id | pubmed-6004993 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Royan Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-60049932018-09-01 Conditioned Medium Protects Dopaminergic Neurons in Parkinsonian Rats Nakhaeifard, Malihe Haji Ghasem Kashani, Maryam Goudarzi, Iran Rezaei, Arezou Cell J Original Article OBJECTIVE: Adipose derived stem cells (ASCs) secrete numerous neurotrophic factors and cytokines in conditioned medium (CM), which protect neurons by its antioxidative and trophic effects. This research assesses the neuroprotective effect of ASC- CM on neurotrophins genes expressions and tyrosine hydroxylase positive (TH+) cell density in male Wistar rats lesioned by 6-hydroxydopamine (6-OHDA). MATERIALS AND METHODS: In this experimental study, the groups consisted of lesioned and sham rats with unilateral injections of 20 µg of 6-OHDA neurotoxin and phosphate buffered saline (PBS) into the striatum, respectively. Another groups received intravenous injections of 3×10(6) cells (ASCs group), 500 µl of CM (ASC-CM group) or medium [α-minimal essential medium (α-MEM) group)]. All rats underwent evaluations with the rotarod and apomorphine-induced rotation tests at 2, 4, 6, and 8 weeks post-injection. At 8 weeks we sacrificed some of the animals for real-time polymerase chain reaction (PCR) analysis, and evaluation of TH+cell counts. RESULTS: We observed a significant decrease in contralateral turns to the lesions in the ASCs and ASC-CM groups compared to the neurotoxin lesioned or α-MEM groups at 8 weeks post transplantation. Cell and CM- injected rats showed a significant increase of staying on the rotarod compared to the lesion or α-MEM groups. Cell and CM-treated rats showed significant increases in the NGF and NT3 genes, respectively, compared with the lesion group. Both treated groups showed significant increases in BDNF gene expression and TH(+) cell density. CONCLUSION: The results suggested that ASCs and ASC-CM protected dopaminergic neurons through the expressions of neurotrophin genes. Royan Institute 2018 2018-05-28 /pmc/articles/PMC6004993/ /pubmed/29845788 http://dx.doi.org/10.22074/cellj.2018.5343 Text en Any use, distribution, reproduction or abstract of this publication in any medium, with the exception of commercial purposes, is permitted provided the original work is properly cited http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nakhaeifard, Malihe Haji Ghasem Kashani, Maryam Goudarzi, Iran Rezaei, Arezou Conditioned Medium Protects Dopaminergic Neurons in Parkinsonian Rats |
title | Conditioned Medium Protects Dopaminergic Neurons in
Parkinsonian Rats |
title_full | Conditioned Medium Protects Dopaminergic Neurons in
Parkinsonian Rats |
title_fullStr | Conditioned Medium Protects Dopaminergic Neurons in
Parkinsonian Rats |
title_full_unstemmed | Conditioned Medium Protects Dopaminergic Neurons in
Parkinsonian Rats |
title_short | Conditioned Medium Protects Dopaminergic Neurons in
Parkinsonian Rats |
title_sort | conditioned medium protects dopaminergic neurons in
parkinsonian rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6004993/ https://www.ncbi.nlm.nih.gov/pubmed/29845788 http://dx.doi.org/10.22074/cellj.2018.5343 |
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