Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American women

Abstract Postmenopausal African American women are at elevated risk for metabolic syndrome (MetS), which predisposes them to cardiovascular disease and other chronic diseases. Circulating microRNAs (ci‐miR) are potential mediators of cardiometabolic diseases also impacted by cardiorespiratory fitnes...

Full description

Bibliographic Details
Main Authors: Ryan M. Sapp, Daniel D. Shill, Chiranjeev Dash, Jennifer C. Hicks, Lucile L. Adams‐Campbell, James M. Hagberg
Format: Article
Language:English
Published: Wiley 2019-07-01
Series:Physiological Reports
Subjects:
Online Access:https://doi.org/10.14814/phy2.14173
id doaj-6e9a0e09b0c24f409591e846d4d778e0
record_format Article
spelling doaj-6e9a0e09b0c24f409591e846d4d778e02020-11-25T02:53:04ZengWileyPhysiological Reports2051-817X2019-07-01714n/an/a10.14814/phy2.14173Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American womenRyan M. Sapp0Daniel D. Shill1Chiranjeev Dash2Jennifer C. Hicks3Lucile L. Adams‐Campbell4James M. Hagberg5Department of Kinesiology, School of Public Health University of Maryland College Park MarylandDepartment of Kinesiology, School of Public Health University of Maryland College Park MarylandGeorgetown Lombardi Comprehensive Cancer Center, Office of Minority Health & Health Disparities Research Washington District of ColumbiaGeorgetown Lombardi Comprehensive Cancer Center, Office of Minority Health & Health Disparities Research Washington District of ColumbiaGeorgetown Lombardi Comprehensive Cancer Center, Office of Minority Health & Health Disparities Research Washington District of ColumbiaDepartment of Kinesiology, School of Public Health University of Maryland College Park MarylandAbstract Postmenopausal African American women are at elevated risk for metabolic syndrome (MetS), which predisposes them to cardiovascular disease and other chronic diseases. Circulating microRNAs (ci‐miR) are potential mediators of cardiometabolic diseases also impacted by cardiorespiratory fitness (CRF) level. Using real‐time quantitative PCR, we compared the expression of vascular‐related ci‐miRs (miR‐21‐5p, miR‐92a‐3p, miR‐126‐5p, miR‐146a‐5p, miR‐150‐5p, miR‐221‐3p) in sedentary, overweight/obese, postmenopausal African American women based on 1) presence (n = 31) or absence (n = 42) of MetS and 2) CRF level (VO2peak) (Very Low < 18.0 mL·kg−1·min−1 [n = 31], Low = 18.0–22.0 mL·kg−1·min−1 [n = 24], or Moderate >22.0 mL·kg−1·min−1 [n = 18]). Endothelial migration rate in response to subjects’ serum was assessed to determine the effect of circulating blood‐borne factors on endothelial repair. Ci‐miR‐21‐5p was the only ci‐miR that differed between women with MetS compared to those without MetS (0.93 ± 0.43 vs. 1.28 ± 0.71, P = 0.03). There were borderline significant differences (P = 0.06–0.09) in ci‐miR‐21‐5p, 126‐5p, and 221‐3p levels between the CRF groups, and these three ci‐miRs correlated with VO2peak (r = −0.25 to −0.28, P < 0.05). Endothelial migration rate was impaired in response to serum from women with MetS compared to those without after 16–24 h. Serum from women with Moderate CRF induced greater endothelial migration than the Very Low and Low CRF groups after 4 and 16–24 h, that was also not different from a young, healthy reference group. Ci‐miR‐21‐5p is lower in postmenopausal African American women with MetS, while ci‐miRs‐21‐5p, 126‐5p, and 221‐3p are associated with CRF. Factors which impair endothelial cell migration rate are present in serum of women with MetS, though having Moderate CRF may be protective.https://doi.org/10.14814/phy2.14173Cardiorespiratory fitnesscirculating microRNAendotheliummenopausemetabolic syndrome
collection DOAJ
language English
format Article
sources DOAJ
author Ryan M. Sapp
Daniel D. Shill
Chiranjeev Dash
Jennifer C. Hicks
Lucile L. Adams‐Campbell
James M. Hagberg
spellingShingle Ryan M. Sapp
Daniel D. Shill
Chiranjeev Dash
Jennifer C. Hicks
Lucile L. Adams‐Campbell
James M. Hagberg
Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American women
Physiological Reports
Cardiorespiratory fitness
circulating microRNA
endothelium
menopause
metabolic syndrome
author_facet Ryan M. Sapp
Daniel D. Shill
Chiranjeev Dash
Jennifer C. Hicks
Lucile L. Adams‐Campbell
James M. Hagberg
author_sort Ryan M. Sapp
title Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American women
title_short Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American women
title_full Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American women
title_fullStr Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American women
title_full_unstemmed Circulating microRNAs and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal African American women
title_sort circulating micrornas and endothelial cell migration rate are associated with metabolic syndrome and fitness level in postmenopausal african american women
publisher Wiley
series Physiological Reports
issn 2051-817X
publishDate 2019-07-01
description Abstract Postmenopausal African American women are at elevated risk for metabolic syndrome (MetS), which predisposes them to cardiovascular disease and other chronic diseases. Circulating microRNAs (ci‐miR) are potential mediators of cardiometabolic diseases also impacted by cardiorespiratory fitness (CRF) level. Using real‐time quantitative PCR, we compared the expression of vascular‐related ci‐miRs (miR‐21‐5p, miR‐92a‐3p, miR‐126‐5p, miR‐146a‐5p, miR‐150‐5p, miR‐221‐3p) in sedentary, overweight/obese, postmenopausal African American women based on 1) presence (n = 31) or absence (n = 42) of MetS and 2) CRF level (VO2peak) (Very Low < 18.0 mL·kg−1·min−1 [n = 31], Low = 18.0–22.0 mL·kg−1·min−1 [n = 24], or Moderate >22.0 mL·kg−1·min−1 [n = 18]). Endothelial migration rate in response to subjects’ serum was assessed to determine the effect of circulating blood‐borne factors on endothelial repair. Ci‐miR‐21‐5p was the only ci‐miR that differed between women with MetS compared to those without MetS (0.93 ± 0.43 vs. 1.28 ± 0.71, P = 0.03). There were borderline significant differences (P = 0.06–0.09) in ci‐miR‐21‐5p, 126‐5p, and 221‐3p levels between the CRF groups, and these three ci‐miRs correlated with VO2peak (r = −0.25 to −0.28, P < 0.05). Endothelial migration rate was impaired in response to serum from women with MetS compared to those without after 16–24 h. Serum from women with Moderate CRF induced greater endothelial migration than the Very Low and Low CRF groups after 4 and 16–24 h, that was also not different from a young, healthy reference group. Ci‐miR‐21‐5p is lower in postmenopausal African American women with MetS, while ci‐miRs‐21‐5p, 126‐5p, and 221‐3p are associated with CRF. Factors which impair endothelial cell migration rate are present in serum of women with MetS, though having Moderate CRF may be protective.
topic Cardiorespiratory fitness
circulating microRNA
endothelium
menopause
metabolic syndrome
url https://doi.org/10.14814/phy2.14173
work_keys_str_mv AT ryanmsapp circulatingmicrornasandendothelialcellmigrationrateareassociatedwithmetabolicsyndromeandfitnesslevelinpostmenopausalafricanamericanwomen
AT danieldshill circulatingmicrornasandendothelialcellmigrationrateareassociatedwithmetabolicsyndromeandfitnesslevelinpostmenopausalafricanamericanwomen
AT chiranjeevdash circulatingmicrornasandendothelialcellmigrationrateareassociatedwithmetabolicsyndromeandfitnesslevelinpostmenopausalafricanamericanwomen
AT jenniferchicks circulatingmicrornasandendothelialcellmigrationrateareassociatedwithmetabolicsyndromeandfitnesslevelinpostmenopausalafricanamericanwomen
AT lucileladamscampbell circulatingmicrornasandendothelialcellmigrationrateareassociatedwithmetabolicsyndromeandfitnesslevelinpostmenopausalafricanamericanwomen
AT jamesmhagberg circulatingmicrornasandendothelialcellmigrationrateareassociatedwithmetabolicsyndromeandfitnesslevelinpostmenopausalafricanamericanwomen
_version_ 1724726914609840128