» Articles » PMID: 7429635

New Phenotypic Marker for Lipopolysaccharide Responsiveness

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

Lipopolysaccharide-enhanced secretion of non-immunoglobulin proteins by bone marrow cells derived from responder, nonresponder, and low-responder mouse strains did not precisely correlate with the lipopolysaccharide responsiveness assessment based on the mitogenic reactivity of splenocytes. These findings suggest that enhancement of secretion of non-immunoglobulin protein may be useful for further characterization of lipopolysaccharide responsiveness.

References
1.
Watson J, Largen M, McAdam K . Genetic control of endotoxic responses in mice. J Exp Med. 1978; 147(1):39-49. PMC: 2184109. DOI: 10.1084/jem.147.1.39. View

2.
Zimmerman D, Okumura K, Rabkin C, Kern M . Differentiation of lymphoid cells: the use of specific antisera to characterize the cells required for the induction of immunoglobulin M production in vitro. J Immunol. 1974; 113(6):1891-6. View

3.
Buckingham R, Castor C . The effect of bacterial products on synovial fibroblast function: hypermetabolic changes induced by endotoxin. J Clin Invest. 1972; 51(5):1186-94. PMC: 292249. DOI: 10.1172/JCI106912. View

4.
SCHER I, Steinberg A, Berning A, Paul W . X-linked B-lymphocyte immune defect in CBA/N mice. II. Studies of the mechanisms underlying the immune defect. J Exp Med. 1975; 142(3):637-50. PMC: 2189918. DOI: 10.1084/jem.142.3.637. View

5.
Zimmerman D, Kern M . Differentiation of lymphoid cells: effect of serum and other mitogenic agents on the selective induction of immunoglobulin M secreting lymph node cells in tissue culture. J Immunol. 1973; 111(5):1326-33. View