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Selenoprotein expression is essential in endothelial cell development and cardiac muscle function

  • Rajeev K. Shrimali
    ,
  • James A. Weaver
    ,
  • Georgina F. Miller
    ,
  • Matthew F. Starost
    ,
  • Bradley A. Carlson
    ,
  • Sergey V. Novoselov
*Corresponding author for this work
  • National Institutes of Health
    ,
  • Intramural Research Program
    ,
  • University of Nebraska-Lincoln
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

LoxP-Cre technology was used to remove the selenocysteine tRNA gene, trsp, in either endothelial cells or myocytes of skeletal and heart muscle to elucidate the role of selenoproteins in cardiovascular disease. Loss of selenoprotein expression in endothelial cells was embryonic lethal. A 14.5-day-old embryo had numerous abnormalities including necrosis of the central nervous system, subcutaneous hemorrhage and erythrocyte immaturity. Loss of selenoprotein expression in myocytes manifested no apparent phenotype until about day 12 after birth. Affected mice had decreased mobility and an increased respiratory rate, which proceeded rapidly to death. Pathological analysis revealed that mice lacking trsp had moderate to severe myocarditis with inflammation extending into the mediastinitis. Thus, ablation of selenoprotein expression demonstrated an essential role of selenoproteins in endothelial cell development and in proper cardiac muscle function. The data suggest a direct connection between the loss of selenoprotein expression in these cell types and cardiovascular disease.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 135-142 (8 pages)

Journal (Volume, Issue Number)

Neuromuscular Disorders (Volume 17, Issue 2)

Publication milestones

  • Published - 02/2007

Publication status

Published - 02/2007

ISSN

0960-8966

Publication IDs

  • Scopus: 33847191027
  • PubMed: 17142041

Publication metrics

Metrics

Fractional count
1
Fractional count
0.11
Fractional count
8
Fractional count
0.89
Fractional count
1
Fractional count
1
SciVal
FWCI
1.63
SciVal
Author count
9
SciVal
citations
27
SciVal
Paper percentile
79
Scopus
citations

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Mentions
2
Citation count
32
Captures
34

Funding Details

This research was supported by the Intramural Research Program of the National Institutes of Health, NCI, Center for Cancer Research and by Grants GM065204 and CA080946 (to V.N.G.).
FundersFunding numbers
NIH
-
NCI
GM065204, CA080946, Z01BC005317