HIGH PLASMA INSULIN-LIKE GROWTH FACTOR-II AND LOW LIPID-CONTENT IN TRANSGENIC MICE - MEASUREMENTS OF LIPID-METABOLISM

被引:42
作者
DACOSTA, THM
WILLIAMSON, DH
WARD, A
BATES, P
FISHER, R
RICHARDSON, L
HILL, DJ
ROBINSON, ICAF
GRAHAM, CF
机构
[1] UNIV OXFORD,DEPT ZOOL,CANC RES CAMPAIGN GROWTH FACTORS,OXFORD OX1 3PS,ENGLAND
[2] RADCLIFFE INFIRM,NUFFIELD DEPT CLIN MED,METAB RES LAB,OXFORD OX2 6HE,ENGLAND
[3] LAWSON RES INST,LONDON N6A 4V2,ON,CANADA
[4] NATL INST MED RES,LONDON NW7 1AA,ENGLAND
关键词
D O I
10.1677/joe.0.1430433
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Transgenic mice were made by introducing extra copies of the mouse insulin-like growth factor-II (IGF-II) gene driven by the bovine keratin 10 promoter (BKVI). The adult plasma IGF-II levels were elevated at least three times in one line. In this line, there was a lower lipid content of both brown and white adipose depots at 2-4 months of age, and 40% less fat in the carcass at 7-9 months. The low lipid phenotype was not detected in the carcass at 2 weeks after birth. The lean characteristic was attributed to circulating IGF-II because the transgene was not expressed in fat. At 2-4 months of age, the transgenes oxidized more oral lipid, and less of this lipid was incorporated into the whole body and the epididymal fat. In contrast, the interscapular brown adipose tissue maintained lipid incorporation and lipoprotein lipase activity despite its reduced size. The altered activity of the brown adipose tissue may account for the gradual onset and persistence of the lean feature of the transgenic mice. There were no substantial changes in lipogenesis which could account for the low fat content. The plasma levels of IGF-I, insulin, glycerol, non-esterified fatty acids, triacylglycerols and glucose were not greatly changed and the pituitary GH content was within the normal range.
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收藏
页码:433 / 439
页数:7
相关论文
共 38 条
[1]   CELLULAR AND MOLECULAR ASPECTS OF ADIPOSE-TISSUE DEVELOPMENT [J].
AILHAUD, G ;
GRIMALDI, P ;
NEGREL, R .
ANNUAL REVIEW OF NUTRITION, 1992, 12 :207-233
[2]  
[Anonymous], 1986, MANIPULATING MOUSE E
[3]  
Ashcroft F., 1992, INSULIN MOL BIOL PAT
[4]  
BANG P, 1992, INSULIN LIKE GROWTH, P151
[5]   EPIGENETIC MECHANISMS UNDERLYING THE IMPRINTING OF THE MOUSE H19-GENE [J].
BARTOLOMEI, MS ;
WEBBER, AL ;
BRUNKOW, ME ;
TILGHMAN, SM .
GENES & DEVELOPMENT, 1993, 7 (09) :1663-1673
[6]   DIFFERENTIALLY EXPRESSED BOVINE CYTOKERATIN GENES - ANALYSIS OF GENE LINKAGE AND EVOLUTIONARY CONSERVATION OF 5'-UPSTREAM SEQUENCES [J].
BLESSING, M ;
ZENTGRAF, H ;
JORCANO, JL .
EMBO JOURNAL, 1987, 6 (03) :567-575
[7]   EFFECTS OF A FRAGMENT OF HUMAN GROWTH HORMONE-RELEASING FACTOR IN NORMAL AND LITTLE MICE [J].
CLARK, RG ;
ROBINSON, ICAF .
JOURNAL OF ENDOCRINOLOGY, 1985, 106 (01) :1-5
[8]   SOMATOMEDIN - PROPOSED DESIGNATION FOR SULFATION FACTOR [J].
DAUGHADAY, WH ;
SALMON, WD ;
VANDENBR.JL ;
VANWYK, JJ ;
RABEN, MS ;
HALL, K .
NATURE, 1972, 235 (5333) :107-+
[9]  
DAUGHADAY WH, 1992, INSULIN LIKE GROWTH, P5
[10]   GROWTH-HORMONE DEFICIENCY IN LITTLE MICE RESULTS IN ABERRANT BODY-COMPOSITION, REDUCED INSULIN-LIKE GROWTH FACTOR-I AND INSULIN-LIKE GROWTH FACTOR-BINDING PROTEIN-3 (IGFBP-3), BUT DOES NOT AFFECT IGFBP-2, IGFBP-1 OR IGFBP-4 [J].
DONAHUE, LR ;
BEAMER, WG .
JOURNAL OF ENDOCRINOLOGY, 1993, 136 (01) :91-104