Characterization of the syngeneic SJL helper T-lymphoma cell interaction and the resulting growth factor products required for lymphoma growth
Thesis/Dissertation
·
OSTI ID:5473552
B cell lymphomas (RCS) arise with high frequency in 9-13 month old SJL mice, probably from follicular center cells. Repeated additions of {gamma}-irradiated syngeneic lymph node cells (LN{gamma}), allow cultured RCS cells, cRCS-X, to be maintained in vitro indefinitely, while cRCS-X alone fail to grow. Isolated cytokines were assayed for effects on in vitro growth of cRCS-X. Murine (m) interleukin (IL)-5 and human B cell growth factor (hBCGF), exhibiting IL-5-like activity on murine B cells, were each found to promote both short and long term growth of cRCS-X cells. Although IL-1 or IFN-{gamma} alone had minimal growth promoting effects on cRCS-X cells, each synergized with either hBCGF or mIL-5. mIL-5 and hBCGF also induced colony formation by cRCS-X cells in agarose which was augmented by IL-1 or IFN-{gamma}. LN{gamma} synergized with BCGF in this assay, even in the presence of excess IL-1, while IL-5 did not. Anti-IL-5 inhibited the effect of LN{gamma} added alone, and the synergistic effect of LN{gamma} was abolished with anti-IFN-{gamma}. Thus, it was concluded that LN{gamma} contributed both IL-5 and IFN-{gamma}. IL-5 also caused much greater proliferation of normal follicular center B cells than of other B cells isolated from immunized mouse LN. Purified helper T cells from I-E{sup {minus}}, but not I-E{sup +} F{sub 1} hybrids of SJL respond to RCS. However, I-E responsive, V{beta}17a{sup +} T cells, were not essential for responsiveness, and T cells from I-E{sup +} transgenic mice, responded to RCS as did T cells from I-E{sup {minus}} litter mates. Therefore, I-E-like antigens are unlikely to be major T cell stimulating moieties on RCS cells.
- Research Organization:
- New York Univ., NY (United States)
- OSTI ID:
- 5473552
- Country of Publication:
- United States
- Language:
- English
Similar Records
Regulation of immune responses in SJL and F1 hybrid mice by gamma-irradiated syngeneic lymphoma cells
SJL bone marrow-derived macrophages do not have IRF3 mutations and are highly susceptible to Theiler's virus infection
Reduced expression of IL-12 p35 by SJL/J macrophages responding to Theiler's virus infection is associated with constitutive activation of IRF-3
Journal Article
·
Sat Dec 31 23:00:00 EST 1983
· J. Natl. Cancer Inst.; (United States)
·
OSTI ID:7013574
SJL bone marrow-derived macrophages do not have IRF3 mutations and are highly susceptible to Theiler's virus infection
Journal Article
·
Thu Dec 14 23:00:00 EST 2017
· Virology
·
OSTI ID:22722976
Reduced expression of IL-12 p35 by SJL/J macrophages responding to Theiler's virus infection is associated with constitutive activation of IRF-3
Journal Article
·
Sat Sep 30 00:00:00 EDT 2006
· Virology
·
OSTI ID:20850568
Related Subjects
560120* -- Radiation Effects on Biochemicals
Cells
& Tissue Culture
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ANIMAL CELLS
ANIMALS
BIOASSAY
BIOLOGICAL FUNCTIONS
BIOLOGICAL MATERIALS
BIOSYNTHESIS
BLOOD
BLOOD CELLS
BODY FLUIDS
CONNECTIVE TISSUE CELLS
DISEASES
ELECTROMAGNETIC RADIATION
EXPERIMENTAL NEOPLASMS
GAMMA RADIATION
GROWTH
GROWTH FACTORS
IMMUNE SYSTEM DISEASES
IONIZING RADIATIONS
LEUKOCYTES
LYMPH NODES
LYMPHATIC SYSTEM
LYMPHOCYTES
LYMPHOKINES
LYMPHOMAS
MAMMALS
MATERIALS
MICE
MITOGENS
NEOPLASMS
ORGANIC COMPOUNDS
PROTEINS
RADIATIONS
RODENTS
SOMATIC CELLS
SYNTHESIS
TUMOR CELLS
VERTEBRATES
Cells
& Tissue Culture
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ANIMAL CELLS
ANIMALS
BIOASSAY
BIOLOGICAL FUNCTIONS
BIOLOGICAL MATERIALS
BIOSYNTHESIS
BLOOD
BLOOD CELLS
BODY FLUIDS
CONNECTIVE TISSUE CELLS
DISEASES
ELECTROMAGNETIC RADIATION
EXPERIMENTAL NEOPLASMS
GAMMA RADIATION
GROWTH
GROWTH FACTORS
IMMUNE SYSTEM DISEASES
IONIZING RADIATIONS
LEUKOCYTES
LYMPH NODES
LYMPHATIC SYSTEM
LYMPHOCYTES
LYMPHOKINES
LYMPHOMAS
MAMMALS
MATERIALS
MICE
MITOGENS
NEOPLASMS
ORGANIC COMPOUNDS
PROTEINS
RADIATIONS
RODENTS
SOMATIC CELLS
SYNTHESIS
TUMOR CELLS
VERTEBRATES