2001Unpublished venueRequires access

Study on biolgical properties of hemopoiesis- supporting function and others of human bone marrow stromal cells

Wanc Xiao-dong

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Abstract

Aim To study on biological properties and hemopoiesissupporting function of human bone marrow stromal cells cultured for long-term in vitro. Methods ① Bone marrow stromal cells from fetus, chidren and adults were cultured for long-time in vitro by static adherent wall assay. ② The phenotypes of the stromal cells were analyzed by immunocytochemical staining or FACA. ③ Hemopoietic stem cells in umbilical cord- blood were co-cultured and expanded with the stromal cells at different development stages. Results ① The fibroblast myoid cell lines were established and could be propagated to 10 generations and kept for 6 months, meantime, endothelial cells and macrophoges were obtained. ② The child stromal myoid cells were positive for viementin and negative for Ⅷ factor by immunocytochemical staining and their phenotypes were CD33 -, CD34 -, CD38 - and CDW90+, while the phenotypes of adult stromal cells were CD33-, CD34-, CD38+ and CDW90+. ③ The stromal cellls could support long-time survival or expansion of LTC-ICs. Survival the of LTC-ICs in the stromal cell-supporting system supplemented with SCF, IL-3 and IL-6 was even longer than that in system without stromal cells(P0. 01 ). The productivity rate of LTC-ICs cultured in the stromal cell-supporting system was 2 to 4 times higher than that cultured in system without stromal cells. Conclusion The human bone marrow stromal cells could be cultured for long-time in vitro and have hemopoiesis-supp ortingfunction for the hemopoietic stem cells in cord blood.

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Aim To study on biological properties and hemopoiesissupporting function of human bone marrow stromal cells cultured for long-term in vitro. Methods ① Bone marrow stromal cells from fetus, chidren and adults were cultured for long-time in vitro by static adherent wall assay. ② The phenotypes of the stromal cells were analyzed by immunocytochemical staining or FACA. ③ Hemopoietic stem cells in umbilical cord- blood were co-cultured and expanded with the stromal cells at different development stages. Results ① The fibroblast myoid cell lines were established and could be propagated to 10 generations and kept for 6 months, meantime, endothelial cells and macrophoges were obtained. ② The child stromal myoid cells were positive for viementin and negative for Ⅷ factor by immunocytochemical staining and their phenotypes were CD33 -, CD34 -, CD38 - and CDW90+, while the phenotypes of adult stromal cells were CD33-, CD34-, CD38+ and CDW90+. ③ The stromal cellls could support long-time survival or expansion of LTC-ICs. Survival the of LTC-ICs in the stromal cell-supporting system supplemented with SCF, IL-3 and IL-6 was even longer than that in system without stromal cells(P0. 01 ). The productivity rate of LTC-ICs cultured in the stromal cell-supporting system was 2 to 4 times higher than that cultured in system without stromal cells. Conclusion The human bone marrow stromal cells could be cultured for long-time in vitro and have hemopoiesis-supp ortingfunction for the hemopoietic stem cells in cord blood.

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Available abstract

Aim To study on biological properties and hemopoiesissupporting function of human bone marrow stromal cells cultured for long-term in vitro. Methods ① Bone marrow stromal cells from fetus, chidren and adults were cultured for long-time in vitro by static adherent wall assay. ② The phenotypes of the stromal cells were analyzed by immunocytochemical staining or FACA. ③ Hemopoietic stem cells in umbilical cord- blood were co-cultured and expanded with the stromal cells at different development stages. Results ① The fibroblast myoid cell lines were established and could be propagated to 10 generations and kept for 6 months, meantime, endothelial cells and macrophoges were obtained. ② The child stromal myoid cells were positive for viementin and negative for Ⅷ factor by immunocytochemical staining and their phenotypes were CD33 -, CD34 -, CD38 - and CDW90+, while the phenotypes of adult stromal cells were CD33-, CD34-, CD38+ and CDW90+. ③ The stromal cellls could support long-time survival or expansion of LTC-ICs. Survival the of LTC-ICs in the stromal cell-supporting system supplemented with SCF, IL-3 and IL-6 was even longer than that in system without stromal cells(P0. 01 ). The productivity rate of LTC-ICs cultured in the stromal cell-supporting system was 2 to 4 times higher than that cultured in system without stromal cells. Conclusion The human bone marrow stromal cells could be cultured for long-time in vitro and have hemopoiesis-supp ortingfunction for the hemopoietic stem cells in cord blood.

Key concepts: Stromal cell, CD34, Haematopoiesis, Bone marrow, Lymph node stromal cell, Stem cell, Biology, Cord blood

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