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Loss of serum response factor induces microRNA-mediated apoptosis in intestinal smooth muscle cells

  • C. Park
    ,
  • M. Y. Lee
    ,
  • O. J. Slivano
    ,
  • P. J. Park
    ,
  • S. Ha
    ,
  • R. M. Berent
*Corresponding author for this work
  • University of Nevada, Reno
    ,
  • Wonkwang University
    ,
  • University of Rochester
    ,
  • University of Fukui
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

Serum response factor (SRF) is a transcription factor known to mediate phenotypic plasticity in smooth muscle cells (SMCs). Despite the critical role of this protein in mediating intestinal injury response, little is known about the mechanism through which SRF alters SMC behavior. Here, we provide compelling evidence for the involvement of SRF-dependent microRNAs (miRNAs) in the regulation of SMC apoptosis. We generated SMC-restricted Srf inducible knockout (KO) mice and observed both severe degeneration of SMCs and a significant decrease in the expression of apoptosis-associated miRNAs. The absence of these miRNAs was associated with overexpression of apoptotic proteins, and we observed a high level of SMC death and myopathy in the intestinal muscle layers. These data provide a compelling new model that implicates SMC degeneration via anti-apoptotic miRNA deficiency caused by lack of SRF in gastrointestinal motility disorders.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Article number

e2011

Journal (Volume, Issue Number)

Cell Death and Disease (Volume 6)

Publication milestones

  • Published - 12/03/2015

Publication status

Published - 12/03/2015

Publication IDs

  • Scopus: 84949193349
  • PubMed: 26633717

Publication metrics

Metrics

SciVal
FWCI
0.38
SciVal
Author count
15
SciVal
citations
11
SciVal
Paper percentile
70
Scopus
citations
Fractional count
1
Fractional count
0.07
Fractional count
14
Fractional count
0.93
Fractional count
1
Fractional count
1

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Citation count
22
Captures
17

Funding Details

FunderFunding number
NIDDK
R01DK103055