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Analyzing hematopoietic development of mouse embryonic AGM region by tissue culture / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1195-1199, 2011.
Article in Chinese | WPRIM | ID: wpr-261902
ABSTRACT
To analyze hematopoietic kinetics of mouse embryonic aorta-gonad-mesonephros (AGM) region, an in vitro tissue culture method was developed in this study, partly based on previous reports. After 2 days of tissue culture, a significant number of erythro myeloid progenitors, as quantitated by colony forming assay was detected in the AGM region. Moreover, the cells from cultured E10.5 AGM region could generate 10.8 ± 3.5 colony-forming unit in spleen (CFU-S) per tissue on average. Transplantation of cultured E10.5-E11.0 AGM cells resulted in efficient (85.7% repopulated) and long-term (> 4 months) reconstitution of lethally irradiated adult recipients with remarkable chimerism [(51.12 ± 21.17)%]. The multilineage contribution of donor cells was validated by significant engraftment of myeloid and/or lymphoid cells in peripheral blood, bone marrow, spleen and thymus of recipients. Taken together, the tissue culture method can enable us to manipulate the AGM region in vitro, fulfilling a systematic evaluation of developmental kinetics of various hematopoietic precursor cells, particularly HSC, in normal and mutant mid-gestation mouse embryos.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Hematopoietic Stem Cells / Mice, Transgenic / Embryology / Cell Biology / Tissue Culture Techniques / Gonads / Hematopoiesis / Hematopoietic System / Methods / Mice, Inbred C57BL Limits: Animals Language: Chinese Journal: Journal of Experimental Hematology Year: 2011 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Hematopoietic Stem Cells / Mice, Transgenic / Embryology / Cell Biology / Tissue Culture Techniques / Gonads / Hematopoiesis / Hematopoietic System / Methods / Mice, Inbred C57BL Limits: Animals Language: Chinese Journal: Journal of Experimental Hematology Year: 2011 Type: Article