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Isolation and characterization of mesenchymal stem cells from human amnion and decidua / 대한산부인과학회지
Korean Journal of Obstetrics and Gynecology ; : 1269-1279, 2008.
Artigo em Inglês | WPRIM | ID: wpr-85242
ABSTRACT

OBJECTIVES:

The purpose of this study is to isolate a population of multipotent cells from human amnion and decidua, respectively.

METHODS:

Human placentas (gestational age, 30~42 weeks) were obtained after vaginal or cesarean deliveries. Amnions and deciduas were divided mechanically. The collected cells from the amnion and decidua were cultured. Cultured cells were immunophenotypically characterized. The adipogenic, osteogenic and neurogenic differentiation capacities were tested, and their growth kinetics were analyzed.

RESULTS:

We successfully isolated MSCs from both the amnion and decidua. The phenotype of MSCs cultured from different fetal and maternal parts of the placenta was comparable. The growth kinetics of MSCs derived from amnions and deciduas were similar. Isolated MSCs were differentiated into various cell lines such as adipogenic, osteogenic, myogenic and neurogenic cells.

CONCLUSIONS:

The human amnion and decidua could be an excellent source of MSC because they are easily obtainable after delivery and showed a higher expansion capacity than that of MSCs from adult bone marrow.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fenótipo / Placenta / Cinética / Linhagem Celular / Células Cultivadas / Durapatita / Decídua / Células-Tronco Mesenquimais / Âmnio Limite: Adulto / Feminino / Humanos Idioma: Inglês Revista: Korean Journal of Obstetrics and Gynecology Ano de publicação: 2008 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fenótipo / Placenta / Cinética / Linhagem Celular / Células Cultivadas / Durapatita / Decídua / Células-Tronco Mesenquimais / Âmnio Limite: Adulto / Feminino / Humanos Idioma: Inglês Revista: Korean Journal of Obstetrics and Gynecology Ano de publicação: 2008 Tipo de documento: Artigo