Decellularized Wharton’s Jelly and Amniotic Membrane Demonstrate Potential Therapeutic Implants in Tracheal Defects in Rabbits

Author:

Neto Aloysio Enck1,Foltz Katia Martins1ORCID,Fuchs Thiago2,Gamba Luize Kremer1,Denk Marcos Antonio3ORCID,Silveira Paulo Cesar Lock4ORCID,Nascimento Thatyanne Gradowski do1,Clemencia Alice Machado4,Francisco Julio César1ORCID,Noronha Lucia de1ORCID,Guarita-Souza Luiz César1ORCID

Affiliation:

1. Graduate Program in Health Sciences, School of Medicine, Pontifícia Universidade Católica do Paraná (PUCPR), Curitiba 80215-901, PR, Brazil

2. Veterinary Medicine Undergraduated Program, University of Contestado (UNC), Mafra 89300-000, SC, Brazil

3. Biomedicine Undergraduate Program, School of Medicine and Life Sciences, Pontifícia Universidade Católica do Paraná, Curitiba 80215-901, PR, Brazil

4. Program of Postgraduate in Science of Health, Laboratory of Experimental Physiopathology, Universidade do Extremo Sul Catarinense (UNESC), Criciúma 88806-000, SC, Brazil

Abstract

Background: Tracheal grafts have been investigated for over a century, aiming to replace various lesions. However, tracheal reconstruction surgery remains a challenge, primarily due to anatomical considerations, intraoperative airway management, the technical complexity of reconstruction, and the potential postoperative morbidity and mortality. Due to research development, the amniotic membrane (AM) and Wharton’s Jelly (WJ) arise as alternatives within the new set of therapeutic alternatives. These structures hold significant therapeutic potential for tracheal defects. This study analyzed the capacity of tracheal tissue regeneration after 60 days of decellularized WJ and AM implantation in rabbits submitted to conventional tracheostomy. Methods: An in vivo experimental study was carried out using thirty rabbits separated into three groups (Control, AM, and WJ) (n = 10). The analyses were performed 60 days after surgery through immunohistochemistry. Results: Different immunomarkers related to scar regeneration, such as aggrecan, TGF-β1, and α-SMA, were analyzed. However, they highlighted no significant difference between the groups. Collagen type I, III, and Aggrecan also showed no significant difference between the groups. Conclusions: Both scaffolds appeared to be excellent frameworks for tissue engineering, presenting biocompatibility and a desirable microenvironment for cell survival; however, they did not display histopathological benefits in trachea tissue regeneration.

Publisher

MDPI AG

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