Dihydropyridine receptor gene expression in skeletal muscle from mdx and control mice.
Dihydropyridine receptor gene expression in skeletal muscle from mdx and control mice.
复制标题
mdx 和对照小鼠骨骼肌中二氢吡啶受体基因的表达。
DOI:
10.1016/s0925-4439(97)00079-3
复制
发表时间:
1997
期刊:
影响因子:
--
通讯作者:
Palade,PT
中科院分区:
文献类型:
--
作者:
Péréon,Y;Dettbarn,C;Navarro,J;Noireaud,J;Palade,PT
The expression of isoform-specific dihydropyrine receptor–calcium channel (DHPR) α1-subunit genes was investigated in mdx and control mouse diaphragm (DIA) and tibialis anterior (TA). RNase protection assays were carried out with a rat DHPR cDNA probe specific for skeletal muscle and a mouse DHPR cDNA probe specific for cardiac muscle. The level of expression of the gene encoding the cardiac DHPR was very weak in TA muscle from both control and mdx mice. Compared to TA, DIA expressed mRNA for the cardiac isoform at significantly higher levels, but mdx and control mouse DIA levels were similar to one another. In contrast, mRNA expression levels for the DHPR skeletal muscle isoform were lower in control DIA than TA. However, there was a dramatic increase in the expression for the DHPR skeletal muscle isoform in mdx DIA compared with control DIA, reaching the TA expression level, whereas dystrophy did not affect TA expression. [3H ]-PN200-110 binding was used to further assess DIA DHPR expression at the protein level. The density of binding sites for the probe was not significantly affected in DIA muscles of mdx vs. control mice, but it was reduced in older mdx and control mice. The increase in DHPR mRNA levels without a consequent increase in DHPR protein expression could be secondary to possible enhanced protein degradation which occurs in mdx DIA. The altered DHPR expression levels found here do not appear to be responsible for the severe deficits in contractile function of the mdx DIA.
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DOI:
10.1016/0005-2760(72)90034-3
发表时间:
1972-01-01
期刊:
BIOCHIMICA ET BIOPHYSICA ACTA
影响因子:
--
作者:
BILHEIMER, DW;LEVY, RI;EISENBERG, S
通讯作者:
EISENBERG, S
影响因子:
6.5
作者:
W. Fisher;L. Zech;P. Bardalaye;G. Warmke;M. Berman
通讯作者:
M. Berman
影响因子:
6.5
作者:
Babiak,J;Tamachi,H;Johnson,FL;Parks,JS;Rudel,LL
通讯作者:
Rudel,LL
影响因子:
6.5
作者:
M. Berman;M. Hall;R. Levy;S. Eisenberg;D. Bilheimer;R. Phair;R. Goebel
通讯作者:
R. Goebel