Korean J Hematol 1999; 34(1):

Published online March 31, 1999

© The Korean Society of Hematology

조혈모세포원 간의 Long-Term Culture-Initiating Cell의 비교

김정아, 김동욱, 이종욱, 한치화, 민우성, 김춘추, 김동집, 홍대식, 박희숙, 김숙자

가톨릭대학교 의과대학 가톨릭 골수이식센터,
순천향대학교 의과대학 내과학교실,임상분자생물학연구소

Direct Comparsion of Long-Term Culture-Initiating Cells in Bone Marrow, Umbilical Cord Blood and Perlpheral Blood Stem Cells

Jeong A Kim, Dong, Wook Kim, Jong Wook Lee, Chi Wha Han, Woo Sung Min, Chun Choo Kim, Dong Jip Kim, Dae Sik Hong, Hee Sook Park, Sook Ja Kim

The Catholic University, Catholic BMT Center
Department of Internal Medicine and Institute for Clinical Molecular Biology Research, Soonchunhyang University, College of Medicine, Seoul, Korea

Abstract

Background: Classically bone marrow(BM) is the maior source of hsmatopoietic stem cells for the transplantation. Recently, hematopoietic stem cells circulating in peripheral
nlood and umbilical cord stem cells have been widely accepted for use in high doss chmotherapy requiring hematopoietic stem cells support. Number if CFU-GM and
CD34+ cells ars routinely used to assess the engraftment potential of BM aspirates and leukapherssls harvests. However, these parameters predominantly reflect
clonogenic cell activity which might only be relevant to short-term hematopoeitic reconstitution, and not necessarily reflect the hsmatopoeitic stem cell activity capable of sustained engraftment. Long-term culture system is regarded as a quantitative method of estimating hsmatopoietic stem cell activity in clinical samples.
Methods: We enumerated CFU-GM and CD34+ cells in G-CSF mobilized peripheral blood (MPB), BM and umbilical cord blood(UCB). Ws obtained the number of LTC-IC from each of tress hematopoietic stem cell sourcss using the long-term culture system. These parameters have compared between the stem cell sources.
Results: CD34+ calls were detected in MPB, BM, and UCB at incidences of 2.27±1.58%, 0.7과土0.55%, 1.24土0.24% of total mononuclear calls. The highest number
of CD34+ cells were seen in UCB. The colony counts higher in UCB than in MPB and BM. Direct comparison of LTC-IC was made between three sources based on CD34+ cell counts. The total numbers of LTC-IC per 10 5CD34+ cell were 713 for UCB, 263 for BM, 104 for MPB. Thess UCB was superior to BM and MPB by cell all three parameters; CFU-GM, CD34+
LTC-IC.
Conclusion: We speculate that UCB should be better source of hematopoletic stem cell transplanation as well as gene thrapy if it could be expanded.

Keywords LTC-IC, Umbilical cord blood, Bone marrow, Perlpheral blood

Article

Korean J Hematol 1999; 34(1): 71-79

Published online March 31, 1999

Copyright © The Korean Society of Hematology.

조혈모세포원 간의 Long-Term Culture-Initiating Cell의 비교

김정아, 김동욱, 이종욱, 한치화, 민우성, 김춘추, 김동집, 홍대식, 박희숙, 김숙자

가톨릭대학교 의과대학 가톨릭 골수이식센터,
순천향대학교 의과대학 내과학교실,임상분자생물학연구소

Direct Comparsion of Long-Term Culture-Initiating Cells in Bone Marrow, Umbilical Cord Blood and Perlpheral Blood Stem Cells

Jeong A Kim, Dong, Wook Kim, Jong Wook Lee, Chi Wha Han, Woo Sung Min, Chun Choo Kim, Dong Jip Kim, Dae Sik Hong, Hee Sook Park, Sook Ja Kim

The Catholic University, Catholic BMT Center
Department of Internal Medicine and Institute for Clinical Molecular Biology Research, Soonchunhyang University, College of Medicine, Seoul, Korea

Abstract

Background: Classically bone marrow(BM) is the maior source of hsmatopoietic stem cells for the transplantation. Recently, hematopoietic stem cells circulating in peripheral
nlood and umbilical cord stem cells have been widely accepted for use in high doss chmotherapy requiring hematopoietic stem cells support. Number if CFU-GM and
CD34+ cells ars routinely used to assess the engraftment potential of BM aspirates and leukapherssls harvests. However, these parameters predominantly reflect
clonogenic cell activity which might only be relevant to short-term hematopoeitic reconstitution, and not necessarily reflect the hsmatopoeitic stem cell activity capable of sustained engraftment. Long-term culture system is regarded as a quantitative method of estimating hsmatopoietic stem cell activity in clinical samples.
Methods: We enumerated CFU-GM and CD34+ cells in G-CSF mobilized peripheral blood (MPB), BM and umbilical cord blood(UCB). Ws obtained the number of LTC-IC from each of tress hematopoietic stem cell sourcss using the long-term culture system. These parameters have compared between the stem cell sources.
Results: CD34+ calls were detected in MPB, BM, and UCB at incidences of 2.27±1.58%, 0.7과土0.55%, 1.24土0.24% of total mononuclear calls. The highest number
of CD34+ cells were seen in UCB. The colony counts higher in UCB than in MPB and BM. Direct comparison of LTC-IC was made between three sources based on CD34+ cell counts. The total numbers of LTC-IC per 10 5CD34+ cell were 713 for UCB, 263 for BM, 104 for MPB. Thess UCB was superior to BM and MPB by cell all three parameters; CFU-GM, CD34+
LTC-IC.
Conclusion: We speculate that UCB should be better source of hematopoletic stem cell transplanation as well as gene thrapy if it could be expanded.

Keywords: LTC-IC, Umbilical cord blood, Bone marrow, Perlpheral blood

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