Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite

Research output: Contribution to journalJournal articleResearchpeer-review

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Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite. / Henn, Dominic; Chen, Kellen; Fischer, Katharina; Rauh, Annika; Barrera, Janos A; Kim, Yoo-Jin; Martin, Russell A; Hannig, Matthias; Niedoba, Patricia; Reddy, Sashank K; Mao, Hai-Quan; Kneser, Ulrich; Gurtner, Geoffrey C; Sacks, Justin M; Schmidt, Volker J.

In: Advances in Wound Care, Vol. 9, No. 7, 2020, p. 365-377.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Henn, D, Chen, K, Fischer, K, Rauh, A, Barrera, JA, Kim, Y-J, Martin, RA, Hannig, M, Niedoba, P, Reddy, SK, Mao, H-Q, Kneser, U, Gurtner, GC, Sacks, JM & Schmidt, VJ 2020, 'Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite', Advances in Wound Care, vol. 9, no. 7, pp. 365-377. https://doi.org/10.1089/wound.2019.0975

APA

Henn, D., Chen, K., Fischer, K., Rauh, A., Barrera, J. A., Kim, Y-J., Martin, R. A., Hannig, M., Niedoba, P., Reddy, S. K., Mao, H-Q., Kneser, U., Gurtner, G. C., Sacks, J. M., & Schmidt, V. J. (2020). Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite. Advances in Wound Care, 9(7), 365-377. https://doi.org/10.1089/wound.2019.0975

Vancouver

Henn D, Chen K, Fischer K, Rauh A, Barrera JA, Kim Y-J et al. Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite. Advances in Wound Care. 2020;9(7):365-377. https://doi.org/10.1089/wound.2019.0975

Author

Henn, Dominic ; Chen, Kellen ; Fischer, Katharina ; Rauh, Annika ; Barrera, Janos A ; Kim, Yoo-Jin ; Martin, Russell A ; Hannig, Matthias ; Niedoba, Patricia ; Reddy, Sashank K ; Mao, Hai-Quan ; Kneser, Ulrich ; Gurtner, Geoffrey C ; Sacks, Justin M ; Schmidt, Volker J. / Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite. In: Advances in Wound Care. 2020 ; Vol. 9, No. 7. pp. 365-377.

Bibtex

@article{e9b21f8176114be3bb583882eec276f5,
title = "Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite",
abstract = "Objective: To develop a novel approach for tissue engineering of soft-tissue flaps suitable for free microsurgical transfer, using an injectable nanofiber hydrogel composite (NHC) vascularized by an arteriovenous (AV) loop. Approach: A rat AV loop model was used for tissue engineering of vascularized soft-tissue flaps. NHC or collagen-elastin (CE) scaffolds were implanted into isolation chambers together with an AV loop and explanted after 15 days. Saphenous veins were implanted into the scaffolds as controls. Neoangiogenesis, ultrastructure, and protein expression of SYNJ2BP, EPHA2, and FOXC1 were analyzed by immunohistochemistry and compared between the groups. Rheological properties were compared between the two scaffolds and native human adipose tissue. Results: A functional neovascularization was evident in NHC flaps with its amount being comparable with CE flaps. Scanning electron microscopy revealed a strong mononuclear cell infiltration along the nanofibers in NHC flaps and a trend toward higher fiber alignment compared with CE flaps. SYNJ2BP and EPHA2 expression in endothelial cells (ECs) was lower in NHC flaps compared with CE flaps, whereas FOXC1 expression was increased in NHC flaps. Compared with the stiffer CE flaps, the NHC flaps showed similar rheological properties to native human adipose tissue. Innovation: This is the first study to demonstrate the feasibility of tissue engineering of soft-tissue flaps with similar rheological properties as human fat, suitable for microsurgical transfer using an injectable nanofiber hydrogel composite. Conclusions: The injectable NHC scaffold is suitable for tissue engineering of axially vascularized soft-tissue flaps with a solid neovascularization, strong cellular infiltration, and biomechanical properties similar to human fat. Our data indicate that SYNJ2BP, EPHA2, and FOXC1 are involved in AV loop-associated angiogenesis and that the scaffold material has an impact on protein expression in ECs.",
keywords = "Animals, Caproates/chemistry, Disease Models, Animal, Female, Hemorheology, Humans, Hydrogels/chemistry, Lactones/chemistry, Microsurgery, Nanocomposites/chemistry, Nanofibers/chemistry, Neovascularization, Physiologic, Rats, Surgical Flaps/blood supply, Tissue Engineering/methods, Tissue Scaffolds, Wound Closure Techniques/instrumentation",
author = "Dominic Henn and Kellen Chen and Katharina Fischer and Annika Rauh and Barrera, {Janos A} and Yoo-Jin Kim and Martin, {Russell A} and Matthias Hannig and Patricia Niedoba and Reddy, {Sashank K} and Hai-Quan Mao and Ulrich Kneser and Gurtner, {Geoffrey C} and Sacks, {Justin M} and Schmidt, {Volker J}",
note = "Copyright 2020, Copyright {\textcopyright} 2020 by Mary Ann Liebert, Inc., publishers.",
year = "2020",
doi = "10.1089/wound.2019.0975",
language = "English",
volume = "9",
pages = "365--377",
journal = "Advances in Wound Care",
issn = "2162-1918",
publisher = "Mary AnnLiebert, Inc. Publishers",
number = "7",

}

RIS

TY - JOUR

T1 - Tissue Engineering of Axially Vascularized Soft-Tissue Flaps with a Poly-(ɛ-Caprolactone) Nanofiber-Hydrogel Composite

AU - Henn, Dominic

AU - Chen, Kellen

AU - Fischer, Katharina

AU - Rauh, Annika

AU - Barrera, Janos A

AU - Kim, Yoo-Jin

AU - Martin, Russell A

AU - Hannig, Matthias

AU - Niedoba, Patricia

AU - Reddy, Sashank K

AU - Mao, Hai-Quan

AU - Kneser, Ulrich

AU - Gurtner, Geoffrey C

AU - Sacks, Justin M

AU - Schmidt, Volker J

N1 - Copyright 2020, Copyright © 2020 by Mary Ann Liebert, Inc., publishers.

PY - 2020

Y1 - 2020

N2 - Objective: To develop a novel approach for tissue engineering of soft-tissue flaps suitable for free microsurgical transfer, using an injectable nanofiber hydrogel composite (NHC) vascularized by an arteriovenous (AV) loop. Approach: A rat AV loop model was used for tissue engineering of vascularized soft-tissue flaps. NHC or collagen-elastin (CE) scaffolds were implanted into isolation chambers together with an AV loop and explanted after 15 days. Saphenous veins were implanted into the scaffolds as controls. Neoangiogenesis, ultrastructure, and protein expression of SYNJ2BP, EPHA2, and FOXC1 were analyzed by immunohistochemistry and compared between the groups. Rheological properties were compared between the two scaffolds and native human adipose tissue. Results: A functional neovascularization was evident in NHC flaps with its amount being comparable with CE flaps. Scanning electron microscopy revealed a strong mononuclear cell infiltration along the nanofibers in NHC flaps and a trend toward higher fiber alignment compared with CE flaps. SYNJ2BP and EPHA2 expression in endothelial cells (ECs) was lower in NHC flaps compared with CE flaps, whereas FOXC1 expression was increased in NHC flaps. Compared with the stiffer CE flaps, the NHC flaps showed similar rheological properties to native human adipose tissue. Innovation: This is the first study to demonstrate the feasibility of tissue engineering of soft-tissue flaps with similar rheological properties as human fat, suitable for microsurgical transfer using an injectable nanofiber hydrogel composite. Conclusions: The injectable NHC scaffold is suitable for tissue engineering of axially vascularized soft-tissue flaps with a solid neovascularization, strong cellular infiltration, and biomechanical properties similar to human fat. Our data indicate that SYNJ2BP, EPHA2, and FOXC1 are involved in AV loop-associated angiogenesis and that the scaffold material has an impact on protein expression in ECs.

AB - Objective: To develop a novel approach for tissue engineering of soft-tissue flaps suitable for free microsurgical transfer, using an injectable nanofiber hydrogel composite (NHC) vascularized by an arteriovenous (AV) loop. Approach: A rat AV loop model was used for tissue engineering of vascularized soft-tissue flaps. NHC or collagen-elastin (CE) scaffolds were implanted into isolation chambers together with an AV loop and explanted after 15 days. Saphenous veins were implanted into the scaffolds as controls. Neoangiogenesis, ultrastructure, and protein expression of SYNJ2BP, EPHA2, and FOXC1 were analyzed by immunohistochemistry and compared between the groups. Rheological properties were compared between the two scaffolds and native human adipose tissue. Results: A functional neovascularization was evident in NHC flaps with its amount being comparable with CE flaps. Scanning electron microscopy revealed a strong mononuclear cell infiltration along the nanofibers in NHC flaps and a trend toward higher fiber alignment compared with CE flaps. SYNJ2BP and EPHA2 expression in endothelial cells (ECs) was lower in NHC flaps compared with CE flaps, whereas FOXC1 expression was increased in NHC flaps. Compared with the stiffer CE flaps, the NHC flaps showed similar rheological properties to native human adipose tissue. Innovation: This is the first study to demonstrate the feasibility of tissue engineering of soft-tissue flaps with similar rheological properties as human fat, suitable for microsurgical transfer using an injectable nanofiber hydrogel composite. Conclusions: The injectable NHC scaffold is suitable for tissue engineering of axially vascularized soft-tissue flaps with a solid neovascularization, strong cellular infiltration, and biomechanical properties similar to human fat. Our data indicate that SYNJ2BP, EPHA2, and FOXC1 are involved in AV loop-associated angiogenesis and that the scaffold material has an impact on protein expression in ECs.

KW - Animals

KW - Caproates/chemistry

KW - Disease Models, Animal

KW - Female

KW - Hemorheology

KW - Humans

KW - Hydrogels/chemistry

KW - Lactones/chemistry

KW - Microsurgery

KW - Nanocomposites/chemistry

KW - Nanofibers/chemistry

KW - Neovascularization, Physiologic

KW - Rats

KW - Surgical Flaps/blood supply

KW - Tissue Engineering/methods

KW - Tissue Scaffolds

KW - Wound Closure Techniques/instrumentation

U2 - 10.1089/wound.2019.0975

DO - 10.1089/wound.2019.0975

M3 - Journal article

C2 - 32587789

VL - 9

SP - 365

EP - 377

JO - Advances in Wound Care

JF - Advances in Wound Care

SN - 2162-1918

IS - 7

ER -

ID: 329562920