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Megakaryocyte Colony Formation of Fetal Liver Cells

Journal of the Korean Pediatric Society 2002;45(2):247-255.
Published online February 15, 2002.
Megakaryocyte Colony Formation of Fetal Liver Cells
Byung O Kwon1, Hye Young Ju1, Chun Soo Kim1, Dong Seok Jeon2, Jong In Kim3, Heung Sik Kim4
1Department of Pediatrics, Sungkyunkwan University, College of Medicine, Masan, Korea
2Department of Clinical Pathology, Keimyung University, College of Medicine, Taegu, Korea
3Department of Obstetrics & Gynecology, Keimyung University, College of Medicine, Taegu, Korea
4Department of Pediatrics, Keimyung University, College of Medicine, Taegu, Korea
태아 간세포의 거핵구 집락형성
권병오1, 주혜영1, 김천수1, 전동석2, 김종인3, 김흥식4
1성균관대학교 의과대학 소아과학교실
2계명대학교 의과대학 임상병리학교실
3계명대학교 의과대학 산부인과학교실
4계명대학교 의과대학 소아과학교실
Correspondence: 
Chun Soo Kim, Email: chunsoo7@unitel.co.kr
Abstract
Purpose
: This study was undertaken to obtain basic data about the megakaryocyte colony formation of fetal liver cells by using immunocytochemical staining and ex vivo culture with growth factors.
Methods
: The mononuclear cells were isolated from fetal liver and bone marrow with idiopathic thrombocytopenic purpura(ITP) and pancytopenia. These mononuclear cells were cultured in MegaCultTM-C(Stem Cell Tech, Canada) media in the presence of growth factors and CFU-Megakaryocyte(CFU-Mk) colonies were counted on day 12. The expansion of CD34+ and CD41+ cell was analyzed by flow cytometry after 5 days incubation using flask culture.
Results
: The numbers of CFU-Mk colonies of mononuclear cells obtained from fetal liver in the 11th week gestational age were more than those in the 19th week specimens; growth factors could not enhance the colony expansion in all cases. Total numbers of CFU-Mk colony of fetal liver cells were higher than bone marrow from ITP or pancytopenia groups. The numbers of pure or large CFU-Mk colonies of fetal liver cells were also higher than bone marrow specimens. The rate of CD34+ cell expression of fetal liver was increased after flask culture and the enhancement effect of epression was seen only in cases which added thrombopoietin. The rate of CD41+ cell expression of fetal liver was increased after incubation, but the enhancement effect of growth factors was unclear.
Conclusion
: This study revealed good results about the megakaryocyte colony assay of fetal liver mononuclear cells using MegaCultTM-C media. This study suggests that the fetal liver could be a good source of megakaryocytic progenitor cells for clinical application in hematopoietic stem cell transplantation.
Key Words: Hematopoietic stem cells, Fetal liver, CFU-Mk


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