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Influence of high mobility group box 1 on migration of human cord blood CD34(+) cells / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 422-425, 2009.
Artigo em Chinês | WPRIM | ID: wpr-302119
ABSTRACT
The objective of study was to explore the influence of high mobility group box 1 (HMGB1) on migration of cord blood CD34(+) cells and their mechanism of migration. The expressions of receptor for advanced glycation end products (RAGE), toll-like receptor-2 (TLR2) and TLR4 were detected by flow cytometry. The CD34(+) cells in umbilical cord blood (CB) were enriched by MiniMACS and were exposed to various concentration of HMGB1 (10, 50, 100, 1, 000 ng/ml), then the migration effect of HMGB1 on umbilical cord blood (UCB) CD34(+) cell count was determined by microscopy, the chemotactic index was calculated. The CD34(+) cells untreated with HMGB1 were used as control. The results indicated that the purity of the isolated CD34(+) cells was more than 98%. The HMGB1 could promote the migration of CD34(+) cells, and the migration effect of HMGB1 on CD34(+) cells in certain concentrations gradually increased along with raise of concentration, the strongest effect was observed in concentration of 100 ng/ml, there was significant difference as compared with control (p < 0.01). Anti-RAGE antibody partially inhibited the migration effect of HMGB1 on CD34(+) cells. It is concluded that the HMGB1 in certain concentration can enhance migration of CD34(+) cells, which may be mediated through RAGE.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Farmacologia / Receptores Imunológicos / Transdução de Sinais / Movimento Celular / Células Cultivadas / Antígenos CD34 / Biologia Celular / Proteína HMGB1 / Sangue Fetal / Receptor para Produtos Finais de Glicação Avançada Limite: Feminino / Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2009 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Farmacologia / Receptores Imunológicos / Transdução de Sinais / Movimento Celular / Células Cultivadas / Antígenos CD34 / Biologia Celular / Proteína HMGB1 / Sangue Fetal / Receptor para Produtos Finais de Glicação Avançada Limite: Feminino / Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2009 Tipo de documento: Artigo