Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging

Diastolic dysfunction of the heart and decreased compliance of the vasculature and lungs (i.e., increased organ tissue stiffness) are known features of obesity and the metabolic syndrome. Similarly, cardiac diastolic dysfunction is associated with aging. Elevation of the enzyme transglutaminase 2 (T...

Full description

Bibliographic Details
Main Authors: Krishna C. Penumatsa, Ines Falcão-Pires, Sara Leite, Adelino Leite-Moreira, Chinmayee D. Bhedi, Sabina Nasirova, Jing Ma, Roy L. Sutliff, Barry L. Fanburg
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-09-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphys.2020.560019/full
_version_ 1819019372976406528
author Krishna C. Penumatsa
Ines Falcão-Pires
Sara Leite
Adelino Leite-Moreira
Chinmayee D. Bhedi
Sabina Nasirova
Jing Ma
Jing Ma
Roy L. Sutliff
Roy L. Sutliff
Barry L. Fanburg
author_facet Krishna C. Penumatsa
Ines Falcão-Pires
Sara Leite
Adelino Leite-Moreira
Chinmayee D. Bhedi
Sabina Nasirova
Jing Ma
Jing Ma
Roy L. Sutliff
Roy L. Sutliff
Barry L. Fanburg
author_sort Krishna C. Penumatsa
collection DOAJ
description Diastolic dysfunction of the heart and decreased compliance of the vasculature and lungs (i.e., increased organ tissue stiffness) are known features of obesity and the metabolic syndrome. Similarly, cardiac diastolic dysfunction is associated with aging. Elevation of the enzyme transglutaminase 2 (TG2) leads to protein cross-linking and enhanced collagen synthesis and participates as a candidate pathway for development of tissue stiffness. With these observations in mind we hypothesized that TG2 may be elevated in tissues of a rat model of obesity/metabolic syndrome (the ZSF 1 rat) and a mouse model of aging, i.e., the senescent SAMP8 mouse. In the experiments reported here, TG2 expression and activity were found for the first time to be spontaneously elevated in organs from both the ZSF1 rat and the SAMP8 mouse. These observations are consistent with a hypothesis that a TG2-related pathway may participate in the known tissue stiffness associated with cardiac diastolic dysfunction in these two rodent models. The potential TG2 pathway needs better correlation with physiologic dysfunction and may eventually provide novel therapeutic insights to improve tissue compliance.
first_indexed 2024-12-21T03:34:17Z
format Article
id doaj.art-c493d84ab73b45c896c1a9b34ef67050
institution Directory Open Access Journal
issn 1664-042X
language English
last_indexed 2024-12-21T03:34:17Z
publishDate 2020-09-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Physiology
spelling doaj.art-c493d84ab73b45c896c1a9b34ef670502022-12-21T19:17:23ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2020-09-011110.3389/fphys.2020.560019560019Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and AgingKrishna C. Penumatsa0Ines Falcão-Pires1Sara Leite2Adelino Leite-Moreira3Chinmayee D. Bhedi4Sabina Nasirova5Jing Ma6Jing Ma7Roy L. Sutliff8Roy L. Sutliff9Barry L. Fanburg10Pulmonary Critical Care and Sleep Division, Department of Medicine, Tufts Medical Center, Boston, MA, United StatesFaculty of Medicine of the University of Porto, Cardiovascular Research and Development Center, Porto, PortugalFaculty of Medicine of the University of Porto, Cardiovascular Research and Development Center, Porto, PortugalFaculty of Medicine of the University of Porto, Cardiovascular Research and Development Center, Porto, PortugalPulmonary Critical Care and Sleep Division, Department of Medicine, Tufts Medical Center, Boston, MA, United StatesPulmonary Critical Care and Sleep Division, Department of Medicine, Tufts Medical Center, Boston, MA, United StatesDepartment of Medicine, Atlanta Veterans Affairs and Emory University Medical Centers, Atlanta, GA, United StatesDepartment of Medicine, Emory University, Atlanta, GA, United StatesDepartment of Medicine, Atlanta Veterans Affairs and Emory University Medical Centers, Atlanta, GA, United StatesDepartment of Medicine, Emory University, Atlanta, GA, United StatesPulmonary Critical Care and Sleep Division, Department of Medicine, Tufts Medical Center, Boston, MA, United StatesDiastolic dysfunction of the heart and decreased compliance of the vasculature and lungs (i.e., increased organ tissue stiffness) are known features of obesity and the metabolic syndrome. Similarly, cardiac diastolic dysfunction is associated with aging. Elevation of the enzyme transglutaminase 2 (TG2) leads to protein cross-linking and enhanced collagen synthesis and participates as a candidate pathway for development of tissue stiffness. With these observations in mind we hypothesized that TG2 may be elevated in tissues of a rat model of obesity/metabolic syndrome (the ZSF 1 rat) and a mouse model of aging, i.e., the senescent SAMP8 mouse. In the experiments reported here, TG2 expression and activity were found for the first time to be spontaneously elevated in organs from both the ZSF1 rat and the SAMP8 mouse. These observations are consistent with a hypothesis that a TG2-related pathway may participate in the known tissue stiffness associated with cardiac diastolic dysfunction in these two rodent models. The potential TG2 pathway needs better correlation with physiologic dysfunction and may eventually provide novel therapeutic insights to improve tissue compliance.https://www.frontiersin.org/article/10.3389/fphys.2020.560019/fulltransglutaminase 2heartlungobesitymetabolic syndromeaging
spellingShingle Krishna C. Penumatsa
Ines Falcão-Pires
Sara Leite
Adelino Leite-Moreira
Chinmayee D. Bhedi
Sabina Nasirova
Jing Ma
Jing Ma
Roy L. Sutliff
Roy L. Sutliff
Barry L. Fanburg
Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging
Frontiers in Physiology
transglutaminase 2
heart
lung
obesity
metabolic syndrome
aging
title Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging
title_full Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging
title_fullStr Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging
title_full_unstemmed Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging
title_short Increased Transglutaminase 2 Expression and Activity in Rodent Models of Obesity/Metabolic Syndrome and Aging
title_sort increased transglutaminase 2 expression and activity in rodent models of obesity metabolic syndrome and aging
topic transglutaminase 2
heart
lung
obesity
metabolic syndrome
aging
url https://www.frontiersin.org/article/10.3389/fphys.2020.560019/full
work_keys_str_mv AT krishnacpenumatsa increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT inesfalcaopires increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT saraleite increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT adelinoleitemoreira increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT chinmayeedbhedi increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT sabinanasirova increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT jingma increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT jingma increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT roylsutliff increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT roylsutliff increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging
AT barrylfanburg increasedtransglutaminase2expressionandactivityinrodentmodelsofobesitymetabolicsyndromeandaging