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1.
Chinese Journal of Hematology ; (12): 64-67, 2003.
Article in Chinese | WPRIM | ID: wpr-261360

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of ex vivo expansion on the adhesion activities of umbilical cord blood hematopoietic stem and progenitor cells (HSPC).</p><p><b>METHODS</b>Fresh UCB CD(34)(+) cells were cultured in a serum and stroma-free culture system. At day 7, day 10 and day 14, CD(34)(+) cells were re-selected from the expanded products. The expression of adhesion molecules (CAMs) such as VLA-4, VLA-5, LFA-1, ICAM-1, HCAM, L-selectin and PECAM-1, and the adhesion activity of the expanded CD(34)(+) cells were evaluated and compared with those of precultured fresh CD(34)(+) cells.</p><p><b>RESULTS</b>(1) The CD(34)(+) cells expressing homing-related CAMs were increased (from 15-fold increase for CD(34)(+) CD(54)(+) subset to 72-fold increase for CD(34)(+) CD(49e)(+) subset at day 14). (2) The expressions of CD(49d), CD(44), CD(11a) and CD(49e) on the expanded CD(34)(+) cells were increased or sustained the same levels as those on fresh UCB CD(34)(+) cells, while the expression of CD(62L), CD(54) and CD(31) on expanded CD(34)(+) cells declined with the cultivating. (3) Spontaneous adhesion and SDF-1-induced adhesion tended to be increased in the course of the first 10 day's culture.</p><p><b>CONCLUSIONS</b>The culture system used in this study could substantially support the expansion of HSPCs expressing the above CAMs, and the expanded HSPCs would sustain their intrinsic adhesion potentials.</p>


Subject(s)
Humans , Antigens, CD , Antigens, CD34 , Cell Adhesion , Cell Adhesion Molecules , Cell Division , Fetal Blood , Cell Biology , Allergy and Immunology , Metabolism , Flow Cytometry , Hematopoietic Stem Cells , Cell Biology , Allergy and Immunology , Metabolism , Receptors, Lymphocyte Homing
2.
Acta Academiae Medicinae Sinicae ; (6): 7-10, 2002.
Article in Chinese | WPRIM | ID: wpr-280975

ABSTRACT

<p><b>OBJECTIVE</b>To compare the expression of cell adhesion molecules (CAMs) among VLA-4 (CD49 d), VLA-5 (CD49e), LFA-1 (CD11a), L-selectin (CD62L), and PECAM-1 (CD31) which are more related to the homing of hematopoietic stem and progenitor cells (HSPC) on the ex vivo expanded CD34+ subset with that of fresh isolated AC133+ cells.</p><p><b>METHODS</b>AC133+ cells selected from fresh cord blood (CB) samples were cultured in QBSF-60 serum-free media in the presence of Flt-3 ligand + SCF + TPO (FST), with initial addition of IL-3 for up to 2 week. Expansion potential and the expression of above CAMs were evaluated at day 0, day 7, day 10 and day 14.</p><p><b>RESULTS</b>(1) Simultaneously numerical expansion of various HSPC was constantly observed during the culture, and the fold expansion of AC133+ cells and CD34+ cells on day 14 were 33.50 and 64.56 respectively; (2) The number of CD34+ subsets expressing the above adhesions were all increased at different degrees (from 20 fold to 160 fold). (3) The expressions of CD11a, CD49d, and CD49e on ex vivo expanded CD34+ cells were increased as compared to their baseline levels, but the percentage of CD62L+ and CD31+ subpopulations in CD34+ cells were decreased.</p><p><b>CONCLUSIONS</b>Our short-term culture system can not merely support the simultaneous expansion of CB derived AC133+ cells, but the expanded hematopoietic progenitors may well sustained the expression of homing-related adhesion molecules.</p>


Subject(s)
Female , Humans , Pregnancy , AC133 Antigen , Antigens, CD , Antigens, CD34 , Metabolism , Cell Adhesion Molecules , Genetics , Cell Division , Cells, Cultured , Culture Media, Serum-Free , Cytokines , Physiology , Fetal Blood , Cell Biology , Metabolism , Glycoproteins , Metabolism , Hematopoietic Stem Cells , Cell Biology , Metabolism , Interleukin-3 , Pharmacology , Lymphocyte Subsets , Peptides , Metabolism , Receptors, Lymphocyte Homing , Metabolism
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