Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.

Human bone marrow contains two major cell types, hematopoietic stem cells (HSCs) and mesenchymal stem cells (MSCs). MSCs possess self-renewal capacity and pluripotency defined by their ability to differentiate into osteoblasts, chondrocytes, adipocytes and muscle cells. MSCs are also known to differ...

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Autores principales: Atsushi Nagai, Woo K Kim, Hong J Lee, Han S Jeong, Kwang S Kim, Seok H Hong, In H Park, Seung U Kim
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Publicado: Public Library of Science (PLoS) 2007
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spelling oai:doaj.org-article:2388bc2f616549c1b3934f61a7f441ed2021-11-25T06:13:44ZMultilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.1932-620310.1371/journal.pone.0001272https://doaj.org/article/2388bc2f616549c1b3934f61a7f441ed2007-12-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0001272https://doaj.org/toc/1932-6203Human bone marrow contains two major cell types, hematopoietic stem cells (HSCs) and mesenchymal stem cells (MSCs). MSCs possess self-renewal capacity and pluripotency defined by their ability to differentiate into osteoblasts, chondrocytes, adipocytes and muscle cells. MSCs are also known to differentiate into neurons and glial cells in vitro, and in vivo following transplantation into the brain of animal models of neurological disorders including ischemia and intracerebral hemorrhage (ICH) stroke. In order to obtain sufficient number and homogeneous population of human MSCs, we have clonally isolated permanent and stable human MSC lines by transfecting primary cell cultures of fetal human bone marrow MSCs with a retroviral vector encoding v-myc gene. One of the cell lines, HM3.B10 (B10), was found to differentiate into neural cell types including neural stem cells, neurons, astrocytes and oligodendrocytes in vitro as shown by expression of genetic markers for neural stem cells (nestin and Musashi1), neurons (neurofilament protein, synapsin and MAP2), astrocytes (glial fibrillary acidic protein, GFAP) and oligodendrocytes (myelin basic protein, MBP) as determined by RT-PCR assay. In addition, B10 cells were found to differentiate into neural cell types as shown by immunocytochical demonstration of nestin (for neural stem cells), neurofilament protein and beta-tubulin III (neurons) GFAP (astrocytes), and galactocerebroside (oligodendrocytes). Following brain transplantation in mouse ICH stroke model, B10 human MSCs integrate into host brain, survive, differentiate into neurons and astrocytes and induce behavioral improvement in the ICH animals. B10 human MSC cell line is not only a useful tool for the studies of organogenesis and specifically for the neurogenesis, but also provides a valuable source of cells for cell therapy studies in animal models of stroke and other neurological disorders.Atsushi NagaiWoo K KimHong J LeeHan S JeongKwang S KimSeok H HongIn H ParkSeung U KimPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 2, Iss 12, p e1272 (2007)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Atsushi Nagai
Woo K Kim
Hong J Lee
Han S Jeong
Kwang S Kim
Seok H Hong
In H Park
Seung U Kim
Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.
description Human bone marrow contains two major cell types, hematopoietic stem cells (HSCs) and mesenchymal stem cells (MSCs). MSCs possess self-renewal capacity and pluripotency defined by their ability to differentiate into osteoblasts, chondrocytes, adipocytes and muscle cells. MSCs are also known to differentiate into neurons and glial cells in vitro, and in vivo following transplantation into the brain of animal models of neurological disorders including ischemia and intracerebral hemorrhage (ICH) stroke. In order to obtain sufficient number and homogeneous population of human MSCs, we have clonally isolated permanent and stable human MSC lines by transfecting primary cell cultures of fetal human bone marrow MSCs with a retroviral vector encoding v-myc gene. One of the cell lines, HM3.B10 (B10), was found to differentiate into neural cell types including neural stem cells, neurons, astrocytes and oligodendrocytes in vitro as shown by expression of genetic markers for neural stem cells (nestin and Musashi1), neurons (neurofilament protein, synapsin and MAP2), astrocytes (glial fibrillary acidic protein, GFAP) and oligodendrocytes (myelin basic protein, MBP) as determined by RT-PCR assay. In addition, B10 cells were found to differentiate into neural cell types as shown by immunocytochical demonstration of nestin (for neural stem cells), neurofilament protein and beta-tubulin III (neurons) GFAP (astrocytes), and galactocerebroside (oligodendrocytes). Following brain transplantation in mouse ICH stroke model, B10 human MSCs integrate into host brain, survive, differentiate into neurons and astrocytes and induce behavioral improvement in the ICH animals. B10 human MSC cell line is not only a useful tool for the studies of organogenesis and specifically for the neurogenesis, but also provides a valuable source of cells for cell therapy studies in animal models of stroke and other neurological disorders.
format article
author Atsushi Nagai
Woo K Kim
Hong J Lee
Han S Jeong
Kwang S Kim
Seok H Hong
In H Park
Seung U Kim
author_facet Atsushi Nagai
Woo K Kim
Hong J Lee
Han S Jeong
Kwang S Kim
Seok H Hong
In H Park
Seung U Kim
author_sort Atsushi Nagai
title Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.
title_short Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.
title_full Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.
title_fullStr Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.
title_full_unstemmed Multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.
title_sort multilineage potential of stable human mesenchymal stem cell line derived from fetal marrow.
publisher Public Library of Science (PLoS)
publishDate 2007
url https://doaj.org/article/2388bc2f616549c1b3934f61a7f441ed
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