EFFECTS OF DIFFERENT LIPOPROTEINS ON THE PROLIFERATIVE RESPONSE OF INTERLEUKIN-2-ACTIVATED T-LYMPHOCYTES AND LARGE GRANULAR LYMPHOCYTES

被引:8
作者
DESANCTIS, JB
BLANCA, I
BIANCO, NE
机构
[1] Institute of Immunology, Faculty of Medicine, Central University of Venezuela, Sabana Grande, Caracas 1050-A
关键词
CHYLOMICRONS; HIGH-DENSITY LIPOPROTEIN; INTERLEUKIN-2; LARGE GRANULAR LYMPHOCYTES; LOW-DENSITY LIPOPROTEIN; T LYMPHOCYTES; VERY LOW-DENSITY LIPOPROTEIN;
D O I
10.1042/cs0890511
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
1. T lymphocytes and large granular lymphocytes internalized chylomicrons, very low-density lipoprotein, low-density lipoprotein, high-density lipoprotein and acetyl modified low-density lipoprotein through different receptors as assessed by flow cytometry. The observed internalization ranged from 8% to 20%. 2. All lipoproteins induced proliferative responses in T lymphocytes and large granular lymphocytes at optimum concentrations (40 mu g of protein/ml for all lipoproteins except high-density lipoprotein). Chylomicrons, very low-density lipoprotein and low-density lipoprotein increased T-lymphocyte proliferative response by fourfold while inducing respectively a seven-, nine- and sevenfold increment in large granular lymphocytes. Similarly, high-density lipoprotein and acetyl modified low-density lipoprotein respectively induced a nine- and sevenfold increment in T cells and a 17- and eightfold increment in large granular lymphocyte proliferative response. 3. Both cell types internalized more lipoprotein when they were stimulated with interleukin 2, Chylomicrons and low-density lipoprotein internalization was increased threefold and very low-density lipoprotein internalization twofold, while high-density lipoprotein internalization was unchanged in both cell types, Acetyl modified low-density lipoprotein internalization was fourfold higher in large granular lymphocytes only. 4. The proliferative response of interleukin-2 stimulated cells was different from that of unstimulated cells. Chylomicrons and very low-density lipoprotein induced a sixfold increment in T-cell proliferative response but only a fourfold increment in large granular lymphocytes, Low-density lipoprotein and acetyl modified low-density lipoprotein induced respectively a sevenfold and eightfold increment in T cells and a eightfold and threefold increment in large granular lymphocyte proliferative response. High-density lipoprotein did not affect T-lymphocyte proliferative response while inducing a twofold increase in large granular lymphocytes. 5. Lipoproteins are important in the proliferative response of unstimulated and interleukin-2-stimulated cells.
引用
收藏
页码:511 / 519
页数:9
相关论文
共 38 条
[1]   RECEPTOR-MEDIATED UPTAKE AND RETROENDOCYTOSIS OF HIGH-DENSITY LIPOPROTEINS BY CHOLESTEROL-LOADED HUMAN MONOCYTE-DERIVED MACROPHAGES - POSSIBLE ROLE IN ENHANCING REVERSE CHOLESTEROL TRANSPORT [J].
ALAM, R ;
YATSU, FM ;
TSUI, L ;
ALAM, S .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1004 (03) :292-299
[2]   DEGRADATION OF CATIONIZED LOW-DENSITY LIPOPROTEIN AND REGULATION OF CHOLESTEROL-METABOLISM IN HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA FIBROBLASTS [J].
BASU, SK ;
GOLDSTEIN, JL ;
ANDERSON, RGW ;
BROWN, MS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (09) :3178-3182
[3]   LIPOPROTEIN-LIPASE ENHANCES THE BINDING OF CHYLOMICRONS TO LOW-DENSITY-LIPOPROTEIN RECEPTOR-RELATED PROTEIN [J].
BEISIEGEL, U ;
WEBER, W ;
BENGTSSONOLIVECRONA, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8342-8346
[4]   LIPOPROTEIN METABOLISM IN THE MACROPHAGE - IMPLICATIONS FOR CHOLESTEROL DEPOSITION IN ATHEROSCLEROSIS [J].
BROWN, MS ;
GOLDSTEIN, JL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1983, 52 :223-261
[5]  
CHAPPELL DA, 1993, J BIOL CHEM, V268, P14168
[6]  
CUTHBERT JA, 1990, J LIPID RES, V31, P2067
[7]  
CUTHBERT JA, 1989, J BIOL CHEM, V264, P1298
[8]   SUPPRESSION OF LYMPHOID-CELL FUNCTION-INVITRO BY INHIBITION OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE BY LOVASTATIN [J].
CUTTS, JL ;
BANKHURST, AD .
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1989, 11 (08) :863-869
[9]   REVERSAL OF LOVASTATIN-MEDIATED INHIBITION OF NATURAL-KILLER-CELL CYTOTOXICITY BY INTERLEUKIN-2 [J].
CUTTS, JL ;
BANKHURST, AD .
JOURNAL OF CELLULAR PHYSIOLOGY, 1990, 145 (02) :244-252
[10]  
DESANCTIS JB, 1994, IMMUNOLOGY, V83, P232