Optimized dissociation protocol for isolating human glioma stem cells from tumorspheres via fluorescence-activated cell sorting

2016 ◽  
Vol 377 (1) ◽  
pp. 105-115 ◽  
Author(s):  
Donglai Lv ◽  
Qing-hua Ma ◽  
Jiang-jie Duan ◽  
Hai-bo Wu ◽  
Xi-long Zhao ◽  
...  
2017 ◽  
Vol 1864 (10) ◽  
pp. 1605-1617 ◽  
Author(s):  
Xihe Zhao ◽  
Yunhui Liu ◽  
Jian Zheng ◽  
Xiaobai Liu ◽  
Jiajia Chen ◽  
...  

2012 ◽  
Vol 8 (2) ◽  
pp. 187-193
Author(s):  
Zu Bin Zhang ◽  
Xiao Gang Jiang ◽  
Zhong Qin Liang ◽  
Zhen Lun Gu

Blood ◽  
1998 ◽  
Vol 92 (8) ◽  
pp. 2886-2892 ◽  
Author(s):  
Kohki Saitoh ◽  
Ikuo Miura ◽  
Naoto Takahashi ◽  
Akira B. Miura

Myelodysplastic syndrome (MDS) is believed to be a stem-cell disorder involving cytopenia and dysplastic changes in three hematopoietic lineages. However, the involvement of pluripotent stem cells and progenitor cells has not been clarified conclusively. To address this issue, we used fluorescence in situ hybridization (FISH) of blood and bone marrow (BM) smears for mature cells and FISH of cells sorted by fluorescence-activated cell sorting for progenitor cells. Seven patients with MDS associated with trisomy 8 were studied. FISH showed +8 in granulocytes, monocytes, and erythroblasts, but not in lymphocytes. Sorted cells of T (CD3+), B (CD19+), and NK cells (CD3−CD56+) from peripheral blood did not contain +8, nor did CD34+ subpopulations from BM including B (CD34+CD19+), T/NK (CD34+CD7+) progenitors, and pluripotent stem cells (CD34+Thy1+). The +8 chromosome abnormality was identified in stem cells only at the level of colony-forming unit of granulocyte-erythrocyte-macrophage-megakaryocyte (CFU-GEMM; CD34+CD33+). It may thus be concluded that cells affected by trisomy 8 in the context of MDS are at the CFU-GEMM level and that cells of lymphoid lineage are not involved. These results provide new insights into the biology of MDS and suggest that intensive chemotherapy and autologous BM transplantation may become important therapeutic strategies. © 1998 by The American Society of Hematology.


Oncogene ◽  
2014 ◽  
Vol 34 (11) ◽  
pp. 1407-1419 ◽  
Author(s):  
Z Wang ◽  
B Wang ◽  
Y Shi ◽  
C Xu ◽  
H L Xiao ◽  
...  

Blood ◽  
1983 ◽  
Vol 62 (1) ◽  
pp. 124-132 ◽  
Author(s):  
RG Andrews ◽  
B Torok-Storb ◽  
ID Bernstein

Abstract Within the hematopoietic system, monoclonal antibodies reactive with antigenic determinants, expressed in a lineage- and stage-restricted fashion, can be used to map myeloid differentiation. We have generated a series of monoclonal antibodies that reacts with myeloid-associated determinants on committed myeloid stem cells and their progeny. Their reactivity with peripheral blood cells was identified by immunofluorescence assays, with bone marrow cells by fluorescence- activated cell sorting, and with committed hematopoietic progenitor cells by both cytotoxic assays and fluorescence-activated cell sorting. Antibody 1G10, which has previously been reported to react with cells of the granulocytic lineage and with a minor subset of mature monocytes, was shown to react with granulocyte-macrophage colony- forming units (CFU-GM). Three antibodies not previously characterized (T5A7, L4F3, L1B2) were shown to react with both granulocytic and monocytic cells and in fluorescence-activated cell sorting studies to detectably stain granulocytic cells at different stages of maturation. These three antibodies also react with CFU-GM, two (L4F3 and L1B2) reacting with all CFU-GM, while T5A7 reacts with only a portion of the day 7 CFU-GM. Antibody L4F3 also reacts with a portion of erythroid burst-forming units (BFU-E). In contrast, the previously reported antibody 5F1, which reacts with monocytic cells, nucleated erythroid cells, and platelets, was shown to react with erythroid colony-forming units (CFU-E). Potential applications of these antibodies to studies of normal and malignant hematopoiesis are discussed.


2015 ◽  
Vol 35 (2) ◽  
pp. 869-877 ◽  
Author(s):  
ZHIWU WU ◽  
YONG HAN ◽  
YANYAN LI ◽  
XUETAO LI ◽  
TING SUN ◽  
...  

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