ISLET CELLS BUT NOT THYROCYTES ARE SUSCEPTIBLE TO LYSIS BY NK CELLS

被引:3
作者
KITAGAWA, Y
GREINER, DL
REYNOLDS, CW
ORTALDO, JR
TOCCAFONDI, R
HANDLER, ES
VANDERMEIDE, PH
MORDES, JP
ROSSINI, AA
机构
[1] NCI,FREDERICK CTR RES FACIL,BIOL RESPONSE MODIFIERS PROGRAM,FREDERICK,MD 21701
[2] UNIV MASSACHUSETTS,MED CTR,DEPT MED,WORCESTER,MA 01655
[3] UNIV CONNECTICUT,DEPT PATHOL,STORRS,CT 06268
[4] UNIV FLORENCE,MED CLIN 3,METAB RES SECT,I-50121 FLORENCE,ITALY
[5] TNO,INST EXPTL GERONTOL,CTR PRIMATE,RIJSWIJK,NETHERLANDS
关键词
D O I
10.1016/0896-8411(91)90167-B
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
BB rats develop both pancreatic insulitis and lymphocytic thyroiditis, but whereas spontaneous autoimmune diabetes is common, hypothyroidism is rare. Splenic natural killer (NK) cells from acutely diabetic (AD) BB rats and from athymic nude rats are known to be cytotoxic to rat islet cells in vitro. To investigate possible differential tissue susceptibility to lysis by NK cells or their cytokines such as cytolysin (perforin) or NK cytotoxic factor (NKCF), we used an in vitro 51Cr-release assay to measure the cytotoxicity of splenocytes, cytolysin or NKCF against Wistar Furth (WF) and Fischer 344 (F-344) rat islet cells, and FRTL-5 F-344-derived and WRT Wistar-derived rat thyrocytes. The results demonstrated that spleen cells from AD-BB (RT1u) rats and athymic F-344 nude (RT11) rats are cytotoxic to WF (RT1u) islets and F-344 (RT11) islets, but not to FRTL-5 (RT11) or WRT (class IRT11) thyrocytes. WF and F-344 rat spleen cells were not cytotoxic to any of these cells. Thyrocytes are known to express class II molecules on their surface in chronic thyroiditis. We found that treatment of thyrocytes with interferon-gamma (IFN-γ) induced class II expression but did not increase the cytotoxicity of splenocytes against these cells. Cytolysin and NKCF were both cytotoxic to islets in a dose dependent manner, but FRTL-5 thyrocytes were resistant to killing by these cytokines. These findings suggest that islet cells and thyrocytes in vitro are differentially susceptible to lysis by NK cells. © 1991.
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页码:703 / 716
页数:14
相关论文
共 71 条
[1]   THE EFFECT OF CIAMEXONE ON LYMPHOCYTIC THYROIDITIS AND INSULIN-DEPENDENT DIABETES-MELLITUS IN THE BB/WOR RAT [J].
ABEND, S ;
CORMIER, J ;
APPEL, MC ;
LUEPRASITSAKUL, W ;
ALEX, S ;
MORDES, JP ;
USADEL, KH ;
HANDLER, ES ;
ROSSINI, AA ;
BRAVERMAN, LE .
IMMUNOPHARMACOLOGY, 1990, 19 (03) :163-168
[2]   CULTURE OF HORMONE-DEPENDENT FUNCTIONAL EPITHELIAL-CELLS FROM RAT THYROIDS [J].
AMBESIIMPIOMBATO, FS ;
PARKS, LAM ;
COON, HG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3455-3459
[3]  
[Anonymous], STATISTICAL PACKAGE
[4]  
BACH JF, 1988, CLIN EXP IMMUNOL, V72, P1
[5]   CYTOTOXIC T-CELL PRECURSORS WITH LOW-LEVEL CD8 IN THE DIABETES-PRONE BIOBREEDING RAT - IMPLICATIONS FOR GENERATION OF AN AUTOIMMUNE T-CELL REPERTOIRE [J].
BELLGRAU, D ;
LAGARDE, AC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :313-317
[6]   NOREPINEPHRINE AND THYROID-STIMULATING HORMONE INDUCE INOSITOL PHOSPHATE ACCUMULATION IN FRTL-5 CELLS [J].
BONE, EA ;
ALLING, DW ;
GROLLMAN, EF .
ENDOCRINOLOGY, 1986, 119 (05) :2193-2200
[7]   INSULIN STIMULATES CELL-GROWTH OF A NEW STRAIN OF DIFFERENTIATED RAT-THYROID CELLS [J].
BRANDI, ML ;
ROTELLA, CM ;
MAVILIA, C ;
FRANCESCHELLI, F ;
TANINI, A ;
TOCCAFONDI, R .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 1987, 54 (01) :91-103
[8]   INSULIN-DEPENDENT DIABETES-MELLITUS IS ASSOCIATED WITH GENES THAT MAP TO THE RIGHT OF THE CLASS-I RT1 - A LOCUS OF THE MAJOR HISTOCOMPATIBILITY COMPLEX OF THE RAT [J].
COLLE, E ;
GUTTMANN, RD ;
FUKS, A .
DIABETES, 1986, 35 (04) :454-458
[9]  
ELDER ME, 1983, J IMMUNOL, V130, P1723
[10]   PERFORIN IS PRESENT ONLY IN NORMAL ACTIVATED LYT2+ LYMPHOCYTES-T AND NOT IN L3T4+ CELLS, BUT THE SERINE PROTEASE GRANZYME-A IS MADE BY BOTH SUBSETS [J].
GARCIASANZ, JA ;
PLAETINCK, G ;
VELOTTI, F ;
MASSON, D ;
TSCHOPP, J ;
MACDONALD, HR ;
NABHOLZ, M .
EMBO JOURNAL, 1987, 6 (04) :933-938