Characterization of Murine Liver‐Derived Inhibitory Protein
- 1 January 1990
- journal article
- research article
- Published by Wiley in Scandinavian Journal of Immunology
- Vol. 31 (1) , 85-90
- https://doi.org/10.1111/j.1365-3083.1990.tb02746.x
Abstract
Murine liver‐derived inhibitory protein (LIP) capable of inhibiting human lymphocyte proliferation was highly purified from liver extract. Its molecular weight determined by gel filtration and SDS‐PAGE was 105,000 and 38,400 respectively. LIP moved electrophoretically at the gammaglobulin region. Its activity in inhibiting lymphocyte proliferation was temperature‐stable up to 60° C, and pH‐stable between 4 and 11. It was not cytotoxic to lymphocytes as shown in 51 Crrelease experiments. The purified LIP possessed arginase activity.This publication has 24 references indexed in Scilit:
- Lounging in a lysosome: the intracellular lifestyle of Coxiella burnetiiCellular Microbiology, 2007
- Biological and Immunological Characterization of a Human Liver Immunoregulatory ProteinHepatology, 1983
- DEMONSTRATION OF A DOG LIVER IMMUNOSUPPRESSIVE FACTOR ACTIVE IN VITROTransplantation, 1979
- Histamine suppression of human lymphocyte responses to mitogensCellular Immunology, 1978
- Effect of cell-free murine liver extract on lymphocyte blastogenesis in vitroCellular Immunology, 1978
- NATURALLY OCCURRING IMMUNOSUPPRESSIVE AGENTSTransplantation, 1975
- Suppression of the immune response by alpha-fetoprotein on the primary and secondary antibody response.The Journal of Experimental Medicine, 1975
- Interaction between Arginase and l‐Ornithine Carbamoyltransferase in Saccharomyces cerevisiaeEuropean Journal of Biochemistry, 1974
- A lymphocyte-inhibiting factor isolated from normal human liverNature, 1974
- Purification and crystallisation of arginaseBiochimica et Biophysica Acta, 1958