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Alcohol Reduces Arterial Remodeling by Inhibiting Sonic Hedgehog‐Stimulated Stem Cell Antigen‐1 Positive Progenitor Stem Cell Expansion
Author(s) -
Fitzpatrick Emma,
Han Xu,
Liu Weimin,
Corcoran Eoin,
Burtenshaw Denise,
Morrow David,
Helt JayChristian,
Cahill Paul A.,
Redmond Eileen M.
Publication year - 2017
Publication title -
alcoholism: clinical and experimental research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.267
H-Index - 153
eISSN - 1530-0277
pISSN - 0145-6008
DOI - 10.1111/acer.13499
Subject(s) - progenitor cell , sonic hedgehog , cyclopamine , stem cell , patched , microbiology and biotechnology , hedgehog signaling pathway , endothelial progenitor cell , cancer research , biology , signal transduction
Background Cell and molecular mechanisms mediating the cardiovascular effects of alcohol are not fully understood. Our aim was to determine the effect of moderate ethanol (EtOH) on sonic hedgehog (SHh) signaling in regulating possible stem cell antigen‐1 positive (Sca1 + ) progenitor stem cell involvement during pathologic arterial remodeling. Methods Partial ligation or sham operation of the left carotid artery was performed in transgenic Sca1‐enhanced green fluorescent protein (eGFP) mice gavaged with or without “daily moderate” EtOH. Results The EtOH group had reduced adventitial thickening and less neointimal formation, compared to ligated controls. There was expansion of eGFP‐expressing (i.e., Sca1 + ) cells in remodeled vessels postligation (day 14), especially in the neo intima. EtOH treatment reduced the number of Sca1 + cells in ligated vessel cross‐sections concomitant with diminished remodeling, compared to control ligated vessels. Moreover, EtOH attenuated SHh signaling in injured carotids as determined by immunohistochemical analysis of the target genes patched 1 and Gli2, and RT–PCR of whole‐vessel Gli2 mRNA levels. Intraperitoneal injection of ligated Sca1‐eGFP mice with the SHh signaling inhibitor cyclopamine diminished SHh target gene expression, reduced the number of Sca1 + cells, and ameliorated carotid remodeling. EtOH treatment of purified Sca1 + adventitial progenitor stem cells in vitro inhibited SHh signaling, and their rSHh‐induced differentiation to vascular smooth muscle cells. Conclusions EtOH reduces SHh‐responsive Sca1 + progenitor cell myogenic differentiation/expansion in vitro and during arterial remodeling in response to ligation injury in vivo. Regulation of vascular Sca1 + progenitor cells in this way may be an important novel mechanism contributing to alcohol's cardiovascular protective effects.