Abstract |
We established a model of immune-mediated bone marrow (BM) failure in C57BL/6 (B6) mice with 6.5 G total-body irradiation followed by the infusion of 4-10 × 10(6) lymph node (LN) cells/recipient from Friend leukemia virus B/N (FVB) donors. Forty-three percent of animals succumbed, with surviving animals showing marked declines in blood neutrophils, red blood cells, platelets and total BM cells at 8 to 14 days following LN cell infusion. Lowering the total-body irradiation dose to 5 G or altering the LN source from FVB to BALB/cBy donors failed to produce BM destruction. Affected animals showed significant expansion and activation of CD8 T lymphocytes in both the blood and BM; cytotoxic T cells had elevated Fas ligand expression and were oligoclonal, mainly displaying Vβ7 and Vβ17 T cell receptors. There were significant increases in blood plasma interferon γ and tissue necrosis factor α in affected animals. Chemokine ligands CCL3, CCL4, CCL5, CCL20, CXCL2, and CXCL5 and hematopoietic growth factors G-CSF, M-CSF, GM-CSF, VEGF were also elevated. In B6 mice carrying a Fas gene mutation, BM failure was attenuated when they were infused with FVB LN cells. Our model establishes a useful platform to define the roles of individual genes and their products in immune-mediated BM failure.
|
Authors | Jichun Chen, Marie J Desierto, Xingmin Feng, Angélique Biancotto, Neal S Young |
Journal | Experimental hematology
(Exp Hematol)
Vol. 43
Issue 4
Pg. 256-67
(Apr 2015)
ISSN: 1873-2399 [Electronic] Netherlands |
PMID | 25555453
(Publication Type: Journal Article, Research Support, N.I.H., Intramural)
|
Copyright | Published by Elsevier Inc. |
Chemical References |
- Fas Ligand Protein
- fas Receptor
|
Topics |
- Animals
- Apoptosis
- Bone Marrow
(immunology, pathology, radiation effects)
- Fas Ligand Protein
(metabolism)
- Lymphocyte Activation
- Mice
- Mice, Inbred BALB C
- Mice, Inbred C57BL
- T-Lymphocytes
(immunology)
- Whole-Body Irradiation
- fas Receptor
(metabolism)
|