Literature DB >> 35521649

Acute Elution of TGFβ2 Affects the Smooth Muscle Cells in a Compliance-Matched Vascular Graft.

Kenneth J Furdella1, Shinichi Higuchi2, Kang Kim1,2,3,4,5, Tom Doetschman6, William R Wagner1,2,5,7, Jonathan P Vande Geest1,2,4,5.   

Abstract

Transforming growth factor beta 2 (TGFβ2) is a pleiotropic growth factor that plays a vital role in smooth muscle cell (SMC) function. Our prior in vitro work has shown that SMC response can be modulated with TGFβ2 stimulation in a dose dependent manner. In particular, we have shown that increasing concentrations of TGFβ2 shift SMCs from a migratory to a synthetic behavior. In this work, electrospun compliance-matched and hypocompliant TGFβ2-eluting tissue engineered vascular grafts (TEVGs) were implanted into Sprague Dawley rats for 5 days to observe SMC population and collagen production. TEVGs were fabricated using a combined computational and experimental approach that varied the ratio of gelatin:polycaprolactone to be either compliance matched or twice as stiff as rat aorta (hypocompliant). TGFβ2 concentrations of 0, 10, 100 ng/mg were added to both graft types (n = 3 in each group) and imaged in vivo using ultrasound. Histological markers (SMC, macrophage, collagen, and elastin) were evaluated following explanation at 5 days. In vivo ultrasound showed that compliance-matched TEVGs became stiffer as TGFβ2 increased (100 ng/mg TEVGs compared to rat aorta, p < 0.01), while all hypocompliant grafts remained stiffer than control rat aorta. In vivo velocity and diameter were also not significantly different than control vessels. The compliance-matched 10 ng/mg group had an elevated SMC signal (myosin heavy chain) compared to the 0 and 100 ng/mg grafts (p = 0.0009 and 0.0006). Compliance-matched TEVGs containing 100 ng/mg TGFβ2 had an increase in collagen production (p < 0.01), general immune response (p < 0.05), and a decrease in SMC population to the 0 and 10 ng/mg groups. All hypocompliant groups were found to be similar, suggesting a lower rate of TGFβ2 release in these TEVGs. Our results suggest that TGFβ2 can modulate in vivo SMC phenotype over an acute implantation period, which is consistent with our prior in vitro work. To the author's knowledge, this is the first in vivo rat study that evaluates a TGFβ2-eluting TEVG. Impact statement TGFβ2 affects the SMCs in a vascular graft.

Entities:  

Keywords:  Sprague Dawley rat; compliance; eluting; tissue-engineered vascular graft; transforming growth factor beta 2; ultrasound

Mesh:

Substances:

Year:  2022        PMID: 35521649      PMCID: PMC9354035          DOI: 10.1089/ten.TEA.2021.0161

Source DB:  PubMed          Journal:  Tissue Eng Part A        ISSN: 1937-3341            Impact factor:   4.080


  57 in total

1.  Biomechanical Comparison of Glutaraldehyde-Crosslinked Gelatin Fibrinogen Electrospun Scaffolds to Porcine Coronary Arteries.

Authors:  E Tamimi; D C Ardila; D G Haskett; T Doetschman; M J Slepian; R S Kellar; J P Vande Geest
Journal:  J Biomech Eng       Date:  2016-01       Impact factor: 2.097

2.  Regulation and characteristics of vascular smooth muscle cell phenotypic diversity.

Authors:  S S M Rensen; P A F M Doevendans; G J J M van Eys
Journal:  Neth Heart J       Date:  2007       Impact factor: 2.380

3.  Stiffness of Aligned Fibers Regulates the Phenotypic Expression of Vascular Smooth Muscle Cells.

Authors:  Bingcheng Yi; Yanbing Shen; Han Tang; Xianliu Wang; Bin Li; Yanzhong Zhang
Journal:  ACS Appl Mater Interfaces       Date:  2019-02-06       Impact factor: 9.229

4.  Transforming growth factor-β and smooth muscle differentiation.

Authors:  Xia Guo; Shi-You Chen
Journal:  World J Biol Chem       Date:  2012-03-26

5.  Transforming growth factor beta 1: three-dimensional structure in solution and comparison with the X-ray structure of transforming growth factor beta 2.

Authors:  A P Hinck; S J Archer; S W Qian; A B Roberts; M B Sporn; J A Weatherbee; M L Tsang; R Lucas; B L Zhang; J Wenker; D A Torchia
Journal:  Biochemistry       Date:  1996-07-02       Impact factor: 3.162

6.  The innate immune system contributes to tissue-engineered vascular graft performance.

Authors:  Narutoshi Hibino; Dane Mejias; Nicholas Pietris; Ethan Dean; Tai Yi; Cameron Best; Toshiharu Shinoka; Christopher Breuer
Journal:  FASEB J       Date:  2015-02-20       Impact factor: 5.191

Review 7.  Transforming growth factor-beta and the immune response: implications for anticancer therapy.

Authors:  Stephen H Wrzesinski; Yisong Y Wan; Richard A Flavell
Journal:  Clin Cancer Res       Date:  2007-09-15       Impact factor: 12.531

8.  Highly Compliant Vascular Grafts with Gelatin-Sheathed Coaxially Structured Nanofibers.

Authors:  Naveen Nagiah; Richard Johnson; Roy Anderson; Winston Elliott; Wei Tan
Journal:  Langmuir       Date:  2015-11-19       Impact factor: 3.882

Review 9.  Trends in tissue engineering for blood vessels.

Authors:  Judee Grace Nemeno-Guanzon; Soojung Lee; Johan Robert Berg; Yong Hwa Jo; Jee Eun Yeo; Bo Mi Nam; Yong-Gon Koh; Jeong Ik Lee
Journal:  J Biomed Biotechnol       Date:  2012-11-08

10.  Fibulin-4 deficiency increases TGF-β signalling in aortic smooth muscle cells due to elevated TGF-β2 levels.

Authors:  N W M Ramnath; L J A C Hawinkels; P M van Heijningen; L te Riet; M Paauwe; M Vermeij; A H J Danser; R Kanaar; P ten Dijke; J Essers
Journal:  Sci Rep       Date:  2015-11-26       Impact factor: 4.379

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