EXPRESSION OF LIPOPROTEIN-LIPASE MESSENGER-RNA IN RAT-HEART IS LOCALIZED MAINLY TO MESENCHYMAL CELLS AS STUDIED BY INSITU HYBRIDIZATION

被引:12
作者
STEIN, O
STEIN, Y
SCHWARTZ, SP
RESHEF, A
CHAJEKSHAUL, T
BENNAIM, M
FRIEDMAN, G
LEITERSDORF, E
机构
[1] HADASSAH UNIV HOSP,DEPT MED B,LIPID RES LAB,POB 12000,IL-91120 JERUSALEM,ISRAEL
[2] HEBREW UNIV JERUSALEM,HADASSAH MED SCH,DEPT EXPTL MED & CANC RES,IL-91010 JERUSALEM,ISRAEL
来源
ARTERIOSCLEROSIS AND THROMBOSIS | 1991年 / 11卷 / 04期
关键词
LIPOPROTEIN LIPASE MESSENGER-RNA; LIPOPROTEIN LIPASE ACTIVITY; RATS; INSITU HYBRIDIZATION;
D O I
10.1161/01.ATV.11.4.857
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The expression of lipoprotein lipase mRNA (LPL mRNA) was studied in rat hearts by use of a sulfur-35-labeled antisense mRNA probe. Rats were studied under three conditions: fed, fasted, and injected with cholera toxin (an irreversible agonist of adenylate cyclase) and then fasted. The highest LPL activity was found in the hearts of cholera toxin-injected, fasted rats. After injection of cholera toxin, LPL mRNA levels were 3.5-fold higher than those from fed rats. Using in situ hybridization, we studied the site of expression of LPL mRNA under the same three experimental conditions. In sections of hearts from cholera toxin-injected, fasted rats, concentrations of autoradiographic grains, representing the site of LPL mRNA, were seen over interstitial elements, which comprise capillary and perivascular cells. A more diffuse and sparse reaction was seen over cardiac myocytes and was not always distinguishable from background. A similar but much less definitive localization was seen in sections of hearts from fasted rats. The present results indicate that in the rat heart, the main site of LPL synthesis and processing, especially after stimulation with an irreversible agonist of adenylate cyclase, is localized to interstitial elements rather than to adult cardiac myocytes.
引用
收藏
页码:857 / 863
页数:7
相关论文
共 31 条
[1]   ACIDIC AND BASIC FIBROBLAST GROWTH-FACTOR MESSENGER-RNAS ARE EXPRESSED BY SKELETAL-MUSCLE SATELLITE CELLS [J].
ALTERIO, J ;
COURTOIS, Y ;
ROBELIN, J ;
BECHET, D ;
MARTELLY, I .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 166 (03) :1205-1212
[2]  
BLANCHETTE-MACKIE E J, 1989, American Journal of Physiology, V256, pE818
[3]   LIPOPROTEIN-LIPASE - CELLULAR-ORIGIN AND FUNCTIONAL DISTRIBUTION [J].
CAMPS, L ;
REINA, M ;
LLOBERA, M ;
VILARO, S ;
OLIVECRONA, T .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (04) :C673-C681
[4]   TREATMENT OF CARDIAC MYOCYTES WITH 8-(4-CHLOROPHENYLTHIO)-ADENOSINE 3',5'-CYCLIC-MONOPHOSPHATE, FORSKOLIN OR CHOLERA-TOXIN DOES NOT STIMULATE CELLULAR OR HEPARIN-RELEASABLE LIPOPROTEIN-LIPASE ACTIVITIES [J].
CARROLL, R ;
JUHASZ, A ;
SEVERSON, DL .
BIOCHEMICAL JOURNAL, 1990, 270 (02) :391-395
[5]   PRENATAL AND POSTNATAL-DEVELOPMENT OF LIPOPROTEIN-LIPASE AND HEPATIC TRIGLYCERIDE HYDROLASE ACTIVITY IN RAT TISSUES [J].
CHAJEK, T ;
STEIN, O ;
STEIN, Y .
ATHEROSCLEROSIS, 1977, 26 (04) :549-561
[6]   RAT-HEART IN CULTURE AS A TOOL TO ELUCIDATE CELLULAR ORIGIN OF LIPOPROTEIN-LIPASE [J].
CHAJEK, T ;
STEIN, O ;
STEIN, Y .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 488 (01) :140-144
[7]   PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE-C RELEASES LIPOPROTEIN-LIPASE FROM THE HEPARIN RELEASABLE POOL IN RAT-HEART CELL-CULTURES [J].
CHAJEKSHAUL, T ;
HALIMI, O ;
BENNAIM, M ;
STEIN, O ;
STEIN, Y .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1014 (02) :178-183
[8]   ENDOGENOUS PLASMA-LIPOPROTEIN LIPASE ACTIVITY IN FED AND FASTING RATS MAY REFLECT THE FUNCTIONAL POOL OF ENDOTHELIAL LIPOPROTEIN-LIPASE [J].
CHAJEKSHAUL, T ;
FRIEDMAN, G ;
STEIN, O ;
ETIENNE, J ;
STEIN, Y .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 837 (03) :271-278
[9]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[10]   AVIAN ADIPOSE LIPOPROTEIN-LIPASE - CDNA SEQUENCE AND RECIPROCAL REGULATION OF MESSENGER-RNA LEVELS IN ADIPOSE AND HEART [J].
COOPER, DA ;
STEIN, JC ;
STRIELEMAN, PJ ;
BENSADOUN, A .
BIOCHIMICA ET BIOPHYSICA ACTA, 1989, 1008 (01) :92-101