Effect of Bone Marrow Culture In Vitro on Its Protective Action in Irradiated Mice2

2009 ◽  
Vol 20 (3) ◽  
pp. 280-286 ◽  
Author(s):  
A. Faille ◽  
C. Dresch ◽  
O. Poirier ◽  
N. Balitrand ◽  
Y. Najean

Blood ◽  
1981 ◽  
Vol 58 (4) ◽  
pp. 724-732 ◽  
Author(s):  
HM Greenberg ◽  
PE Newburger ◽  
LM Parker ◽  
T Novak ◽  
JS Greenberger

Abstract A long-term bone marrow culture system has been derived for maintenance and proliferation of human hemopoietic stem cells and granulocytes in vitro for up to 20 wk. The granulocytes generated in these cultures at 8 wk were comparable to fresh human peripheral blood granulocytes in physiologic properties, including phagocytosis, degranulation, respiratory burst, and bacterial killing: individual granulocytes generated up to 20 wk in several cultures demonstrated normal superoxide-generating capacity by NBT dye reduction slide test. Thus, human granulocytes generated in continuous marrow culture retain many biologic functions associated with bacterocidal capacity in vivo and indicate that this system should be of value in studies of disorders of granulocyte differentiation.


1987 ◽  
Vol 25 (1) ◽  
pp. 43-53 ◽  
Author(s):  
Daniel J. Weisdorf ◽  
Robert T. Perri ◽  
Martin M. Oken ◽  
Wesley J. Miller ◽  
Diane C. Arthur ◽  
...  

Blood ◽  
1979 ◽  
Vol 54 (4) ◽  
pp. 775-793
Author(s):  
MA Moore ◽  
AP Sheridan ◽  
TD Allen ◽  
TM Dexter

Maintenance of myelopoiesis and pluripotential stem cell production for prolonged periods in vitro hitherto has been limited to mouse bone marrow culture. In an effort to adapt the system for use in higher species, particularly in human and non-human primates, studies were undertaken using the prosimian species, Tupaia glis (tree shrew). In a number of experiments the duration of sustained normal hematopoiesis observed in cultures of this species, following a single inoculum of 5 X 10(6)--10(7) bone marrow cells, with or without addition of fresh allogeneic bone marrow exceeded 1 yr. Analysis of suspension cells obtained by weekly demidepopulation of such cultures revealed production of CFU-C, differentiating neutrophils, and basophils at high levels. Direct comparison with murine cultures indicated that in both species a complex series of cellular interactions takes place within an adherent environment of marrow-derived endothelial cells, macrophages, and fat-containing cells. Certain functional and ultrastructural features served to distinguish murine from Tupaia marrow cultures, and the prolonged duration of in vitro hematopoiesis in the latter species could be attributed to a regenerative capacity possessed by its adherent hematopoietic microenvironment. The availability of this primate marrow culture system should facilitate studies of hematopoiesis, viral leukemogenesis, and transplantation biology, which have more direct relevance to man than that provided by the existing murine system.


2003 ◽  
Vol 18 (8) ◽  
pp. 1471-1477 ◽  
Author(s):  
Ken-Ichi Miyamoto ◽  
Hirokazu Suzuki ◽  
Shinya Yamamoto ◽  
Yukie Saitoh ◽  
Eiji Ochiai ◽  
...  

1989 ◽  
Vol 6 (4) ◽  
pp. 293-305 ◽  
Author(s):  
Ariel Koren Klirlat ◽  
Pnina Bar Sela ◽  
Yigal Barak ◽  
Jeriss Jammalieh ◽  
Eliahu Katzurti

2008 ◽  
Vol 7 (3) ◽  
pp. 5-8
Author(s):  
A. N. Baikov ◽  
V. P. Shakhov ◽  
N. Yu. Shelgaev ◽  
V. A. Serebryakova

Experiments with 60 male and female mice of Balb/c line with mass of 18—21 g have been carried out. All manipulations, including ether euthanasia, were performed within the framework of approved rules for experiments with experimental animals. The mice were divided into four groups each of 15 animals. The groups were injected with physiological salt solution (first group), cycliphosphan (second group), Granotsit preparation (recombinant granulocytic colony-stimulating factor) (third group), and cycliphosphan in Granotsit preparation (fourth group). We have studied the total number of leucocytes in blood, bone marrow cellularity, content of granulocytic- macrophage colony-forming cells and mesenchyma l precursors with the aid of tissue culture in vitro. It has been found that the Granotsit preparation can stimulate myelopoiesis (direct specific action) and mesenchymopo iesis (indirect action) in norm. When a cytostatic agent, the studied cytokine has a protective action on both myeloid and mesenchyma l precursors of bone marrow.


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