Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluid

As the key producer of cerebrospinal fluid (CSF), the choroid plexus (CP) provides a unique protective system in the central nervous system. CSF components are not invariable and they can change based on the pathological conditions of the central nervous system. The purpose of the present study was...

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Main Authors: Elham Hashemi, Yousef Sadeghi, Abbas Aliaghaei, Afsoun Seddighi, Abbas Piryaei, Mehdi Eskandarian Broujeni, Fatemeh Shaerzadeh, Abdollah Amini, Ramin Pouriran
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Neural Regeneration Research
Subjects:
Online Access:http://www.nrronline.org/article.asp?issn=1673-5374;year=2017;volume=12;issue=1;spage=84;epage=89;aulast=Hashemi
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author Elham Hashemi
Yousef Sadeghi
Abbas Aliaghaei
Afsoun Seddighi
Abbas Piryaei
Mehdi Eskandarian Broujeni
Fatemeh Shaerzadeh
Abdollah Amini
Ramin Pouriran
author_facet Elham Hashemi
Yousef Sadeghi
Abbas Aliaghaei
Afsoun Seddighi
Abbas Piryaei
Mehdi Eskandarian Broujeni
Fatemeh Shaerzadeh
Abdollah Amini
Ramin Pouriran
author_sort Elham Hashemi
collection DOAJ
description As the key producer of cerebrospinal fluid (CSF), the choroid plexus (CP) provides a unique protective system in the central nervous system. CSF components are not invariable and they can change based on the pathological conditions of the central nervous system. The purpose of the present study was to assess the effects of non-traumatic and traumatic CSF on the differentiation of multipotent stem-like cells of CP into the neural and/or glial cells. CP epithelial cells were isolated from adult male rats and treated with human non-traumatic and traumatic CSF. Alterations in mRNA expression of Nestin and microtubule-associated protein (MAP2), as the specific markers of neurogenesis, and astrocyte marker glial fibrillary acidic protein (GFAP) in cultured CP epithelial cells were evaluated using quantitative real-time PCR. The data revealed that treatment with CSF (non-traumatic and traumatic) led to increase in mRNA expression levels of MAP2 and GFAP. Moreover, the expression of Nestin decreased in CP epithelial cells treated with non-traumatic CSF, while treatment with traumatic CSF significantly increased its mRNA level compared to the cells cultured only in DMEM/F12 as control. It seems that CP epithelial cells contain multipotent stem-like cells which are inducible under pathological conditions including exposure to traumatic CSF because of its compositions.
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spelling doaj.art-0953338f97e84e48b3832456ec3cf31c2022-12-21T20:10:46ZengWolters Kluwer Medknow PublicationsNeural Regeneration Research1673-53742017-01-01121848910.4103/1673-5374.198989Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluidElham HashemiYousef SadeghiAbbas AliaghaeiAfsoun SeddighiAbbas PiryaeiMehdi Eskandarian BroujeniFatemeh ShaerzadehAbdollah AminiRamin PouriranAs the key producer of cerebrospinal fluid (CSF), the choroid plexus (CP) provides a unique protective system in the central nervous system. CSF components are not invariable and they can change based on the pathological conditions of the central nervous system. The purpose of the present study was to assess the effects of non-traumatic and traumatic CSF on the differentiation of multipotent stem-like cells of CP into the neural and/or glial cells. CP epithelial cells were isolated from adult male rats and treated with human non-traumatic and traumatic CSF. Alterations in mRNA expression of Nestin and microtubule-associated protein (MAP2), as the specific markers of neurogenesis, and astrocyte marker glial fibrillary acidic protein (GFAP) in cultured CP epithelial cells were evaluated using quantitative real-time PCR. The data revealed that treatment with CSF (non-traumatic and traumatic) led to increase in mRNA expression levels of MAP2 and GFAP. Moreover, the expression of Nestin decreased in CP epithelial cells treated with non-traumatic CSF, while treatment with traumatic CSF significantly increased its mRNA level compared to the cells cultured only in DMEM/F12 as control. It seems that CP epithelial cells contain multipotent stem-like cells which are inducible under pathological conditions including exposure to traumatic CSF because of its compositions.http://www.nrronline.org/article.asp?issn=1673-5374;year=2017;volume=12;issue=1;spage=84;epage=89;aulast=Hasheminerve regeneration; choroid plexus; cerebrospinal fluid; stem cells; Nestin; microtubule-associated protein 2; glial fibrillary acidic protein; neurogenesis; central nervous system; neural regeneration
spellingShingle Elham Hashemi
Yousef Sadeghi
Abbas Aliaghaei
Afsoun Seddighi
Abbas Piryaei
Mehdi Eskandarian Broujeni
Fatemeh Shaerzadeh
Abdollah Amini
Ramin Pouriran
Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluid
Neural Regeneration Research
nerve regeneration; choroid plexus; cerebrospinal fluid; stem cells; Nestin; microtubule-associated protein 2; glial fibrillary acidic protein; neurogenesis; central nervous system; neural regeneration
title Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluid
title_full Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluid
title_fullStr Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluid
title_full_unstemmed Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluid
title_short Neural differentiation of choroid plexus epithelial cells: role of human traumatic cerebrospinal fluid
title_sort neural differentiation of choroid plexus epithelial cells role of human traumatic cerebrospinal fluid
topic nerve regeneration; choroid plexus; cerebrospinal fluid; stem cells; Nestin; microtubule-associated protein 2; glial fibrillary acidic protein; neurogenesis; central nervous system; neural regeneration
url http://www.nrronline.org/article.asp?issn=1673-5374;year=2017;volume=12;issue=1;spage=84;epage=89;aulast=Hashemi
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