Title of article :
the effect of platelet lysate on expansion and differentiation megakaryocyte progenitor cells from cord blood cd34^+ enriched cells
Author/Authors :
yaghoubi, yoda tabriz university of medical sciences - student research committee, stem cell research center, tabriz, iran , hassanzadeh, ali tehran university of medical sciences - department of tissue engineering and applied cell sciences, tehran, iran , naimi, adel sabzevar university of medical sciences - cellular and molecular research center, sabzevar, iran , abdolahi, sepehr azarbaijan shahid madani university - faculty of science - department of biology, tabriz, iran , yousefi, mehdi tabriz university of medical sciences - stem cell research center, tabriz, iran , aghebati-maleki, leili tabriz university of medical sciences - immunology research center, tabriz, iran , zamani, majid gonabad university of medical sciences - faculty of allied medicine - department of medical laboratory sciences, gonabad, iran
From page :
172
To page :
182
Abstract :
background: umbilical cord blood hematopoietic stem cells (ucb-hscs) are an attractive source for transplantation. the generation of megakaryocyte- committed cells could lead to shorten period of thrombocytopenia after hscs transplantation. platelet lysate (pl) unlike fetal bovine serum (fbs) can prevent immune problems as well as avert transmission of certain diseases to the recipient. in this study, the authors aimed to assess the effect of pl on ucb cd34+ cells expansion and megakaryocyte differentiation. materials and methods: in this experimental study, pl prepared and the subsequent isolation of ucb cd34+ cells were done by magnetic cell sorting. the isolated cells were cultivated in iscove’s modified dulbecco’s medium (imdm) supplemented with pl or fbs. cell expansion was evaluated using trypan blue. furthermore, flow cytometry using monoclonal antibodies (cd41- fitc and cd42b-pe) and the expression of specific genes including gata1, gata2, fli1, nfe2, and runx1 via real-time pcr were performed to evaluate the megakaryocyte differentiation. results: the results showed that pl insignificantly enhanced ucb cd34^+ cell expansion (32.83± 8.47 fold in fbs and 41.67± 10.31 fold in pl containing media). besides, flow cytometry results showed that expression of cd41 was increased markedly (37.81± 4.78 fold in fbs and 45.78 ± 7.37 in pl containing media, p-value 0.05) but the elevation of cd42b (10.53 ± 2.13 and 13.20 ± 2.06 in fbs and pl containing media, respectively) was not significant (p-value = 0.051). the results of real- time pcr demonstrated a notable increase in gata binding protein 1 (1.58, p-value 0.01), gata binding protein 2 (2.45, p-value 0.001), runx family transcription factor 1 (1.60, p-value 0.01), fli-1 proto-oncogene (1.87, p-value 0.001) in pl supplemented media, however, the increase of nuclear factor-erythroid 2 gene expression was not significant in pl supplemented media (pvalue = 0.11). conclusion: pl improved ucb cd34^+ cells expansion and megakaryocyte differentiation compared to fbs.
Keywords :
cord blood stem cell transplantation , hematopoietic stem cells , megakaryocyte progenitor cells , platelet , derived growth factor
Journal title :
Iranian Journal of Pediatric Hematology and Oncology
Journal title :
Iranian Journal of Pediatric Hematology and Oncology
Record number :
2706018
Link To Document :
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