Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in Adulthood
Postnatal growth restriction (PGR) increases the risk for cardiovascular disease (CVD) in adulthood, yet there is minimal mechanistic rationale for the observed pathology. The purpose of this study was to identify proteomic differences in hearts of growth-restricted and unrestricted mice, and propos...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-12-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/21/24/9459 |
id |
doaj-f5bb7290a9de4f45a95ef880a452f0e6 |
---|---|
record_format |
Article |
spelling |
doaj-f5bb7290a9de4f45a95ef880a452f0e62020-12-13T00:00:35ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-12-01219459945910.3390/ijms21249459Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in AdulthoodJoseph R. Visker0Lawrence J. Dangott1Eric C. Leszczynski2David P. Ferguson3Department of Kinesiology, Michigan State University, East Lansing, MI 48824, USAProtein Chemistry Laboratory, Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843, USADepartment of Kinesiology, Michigan State University, East Lansing, MI 48824, USADepartment of Kinesiology, Michigan State University, East Lansing, MI 48824, USAPostnatal growth restriction (PGR) increases the risk for cardiovascular disease (CVD) in adulthood, yet there is minimal mechanistic rationale for the observed pathology. The purpose of this study was to identify proteomic differences in hearts of growth-restricted and unrestricted mice, and propose mechanisms related to impairment in adulthood. Friend leukemia virus B (FVB) mouse dams were fed a control (CON: 20% protein), or low-protein (LP: 8% protein) isocaloric diet 2 weeks before mating. LP dams produce 20% less milk, inducing growth restriction. At birth (postnatal; PN1), pups born to dams fed the CON diet were switched to LP dams (PGR group) or a different CON dam. At PN21, a sub-cohort of CON (<i>n</i> = 3 males; <i>n</i> = 3 females) and PGR (<i>n</i> = 3 males; <i>n</i> = 3 females) were euthanized and their proteome analyzed by two-dimensional differential in-gel electrophoresis (2D DIGE) and mass spectroscopy. Western blotting and silver nitrate staining confirmed 2D DIGE results. Littermates (CON: <i>n</i> = 4 males and <i>n</i> = 4 females; PGR: <i>n</i> = 4 males and <i>n</i> = 4 females) were weaned to the CON diet. At PN77, echocardiography measured cardiac function. At PN80, hearts were removed for western blotting to determine if differences persisted into adulthood. 2D DIGE and western blot confirmation indicated PGR had reductions in p57<sup>kip2</sup>, Titin (Ttn), and Collagen (Col). At PN77, PGR had impaired cardiac function as measured by echocardiography. At PN80, western blots of p57<sup>kip2</sup> showed protein abundance recovered from PN21. PN80 silver staining of large molecular weight proteins (Ttn and Col) was reduced in PGR. PGR reduces cell cycle activity at PN21, which is recovered in adulthood. However, collagen fiber networks are altered into adulthood.https://www.mdpi.com/1422-0067/21/24/9459DOHaDpostnatal growth restrictioncardiac functionp57<sup>kip2</sup>titincollagen |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Joseph R. Visker Lawrence J. Dangott Eric C. Leszczynski David P. Ferguson |
spellingShingle |
Joseph R. Visker Lawrence J. Dangott Eric C. Leszczynski David P. Ferguson Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in Adulthood International Journal of Molecular Sciences DOHaD postnatal growth restriction cardiac function p57<sup>kip2</sup> titin collagen |
author_facet |
Joseph R. Visker Lawrence J. Dangott Eric C. Leszczynski David P. Ferguson |
author_sort |
Joseph R. Visker |
title |
Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in Adulthood |
title_short |
Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in Adulthood |
title_full |
Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in Adulthood |
title_fullStr |
Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in Adulthood |
title_full_unstemmed |
Postnatal Growth Restriction in Mice Alters Cardiac Protein Composition and Leads to Functional Impairment in Adulthood |
title_sort |
postnatal growth restriction in mice alters cardiac protein composition and leads to functional impairment in adulthood |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2020-12-01 |
description |
Postnatal growth restriction (PGR) increases the risk for cardiovascular disease (CVD) in adulthood, yet there is minimal mechanistic rationale for the observed pathology. The purpose of this study was to identify proteomic differences in hearts of growth-restricted and unrestricted mice, and propose mechanisms related to impairment in adulthood. Friend leukemia virus B (FVB) mouse dams were fed a control (CON: 20% protein), or low-protein (LP: 8% protein) isocaloric diet 2 weeks before mating. LP dams produce 20% less milk, inducing growth restriction. At birth (postnatal; PN1), pups born to dams fed the CON diet were switched to LP dams (PGR group) or a different CON dam. At PN21, a sub-cohort of CON (<i>n</i> = 3 males; <i>n</i> = 3 females) and PGR (<i>n</i> = 3 males; <i>n</i> = 3 females) were euthanized and their proteome analyzed by two-dimensional differential in-gel electrophoresis (2D DIGE) and mass spectroscopy. Western blotting and silver nitrate staining confirmed 2D DIGE results. Littermates (CON: <i>n</i> = 4 males and <i>n</i> = 4 females; PGR: <i>n</i> = 4 males and <i>n</i> = 4 females) were weaned to the CON diet. At PN77, echocardiography measured cardiac function. At PN80, hearts were removed for western blotting to determine if differences persisted into adulthood. 2D DIGE and western blot confirmation indicated PGR had reductions in p57<sup>kip2</sup>, Titin (Ttn), and Collagen (Col). At PN77, PGR had impaired cardiac function as measured by echocardiography. At PN80, western blots of p57<sup>kip2</sup> showed protein abundance recovered from PN21. PN80 silver staining of large molecular weight proteins (Ttn and Col) was reduced in PGR. PGR reduces cell cycle activity at PN21, which is recovered in adulthood. However, collagen fiber networks are altered into adulthood. |
topic |
DOHaD postnatal growth restriction cardiac function p57<sup>kip2</sup> titin collagen |
url |
https://www.mdpi.com/1422-0067/21/24/9459 |
work_keys_str_mv |
AT josephrvisker postnatalgrowthrestrictioninmicealterscardiacproteincompositionandleadstofunctionalimpairmentinadulthood AT lawrencejdangott postnatalgrowthrestrictioninmicealterscardiacproteincompositionandleadstofunctionalimpairmentinadulthood AT ericcleszczynski postnatalgrowthrestrictioninmicealterscardiacproteincompositionandleadstofunctionalimpairmentinadulthood AT davidpferguson postnatalgrowthrestrictioninmicealterscardiacproteincompositionandleadstofunctionalimpairmentinadulthood |
_version_ |
1724385729399750656 |