» Articles » PMID: 30097829

Comparison of Esophageal Submucosal Glands in Experimental Models for Esophagus Tissue Engineering Applications

Overview
Journal Esophagus
Publisher Springer
Date 2018 Aug 12
PMID 30097829
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Esophagus tissue engineering holds promises to overcome the limitations of the presently employed esophageal replacement procedures. This study investigated 5 animal models for esophageal submucosal glands (ESMG) to identify models appropriate for regenerative medicine applications. Furthermore, this study aimed to measure geometric parameters of ESMG that could be utilized for fabrication of ESMG-specific scaffolds for esophagus tissue engineering applications.

Methods: Ovine, avian, bovine, murine, and porcine esophagus were investigated using Hematoxylin-Eosin (HE), Periodic Acid Schiff (PAS), and Alcian Blue (AB), with AB applied in 3 pH levels (0.2, 1.0, and 2.5) to detect sulphated mucous. Celleye (version F) was employed to gain parametric data on ESMGs (size, perimeter, distance to lumen, and acini concentration) necessary for scaffold fabrication.

Results: Murine, bovine, and ovine esophagus were devoid of ESMG. Avian esophagus demonstrated sulphated acid mucous producing ESMGs with a holocrine secretion pattern, whereas sulphated acid and neutral mucous producing ESMGs with a merocrine secretion pattern were observed in porcine esophagus. Distance of ESMGs to lumen ranged from 127-340 μm (avian) to 916-983 μm (porcine). ESMGs comprised 35% (avian) to 45% (porcine) area of the submucosa. ESMG had an area of 125000 μm (avian) to 580000 μm (porcine).

Conclusion: Avian and porcine esophagus possesses ESMGs. However, porcine esophagus correlates with data available on human ESMGs. Geometric and parametric data obtained from ESMG are valuable for the fabrication of ESMG-specific scaffolds for esophagus tissue engineering using the hybrid construct approach.

Citing Articles

New aspects of the esophageal histology of the domestic goat (Capra hircus) and European roe deer (Capreolus capreolus).

Sokolowska J, Urbanska K, Matusiak J, Wisniewski J Vet Med Sci. 2021; 7(5):1743-1756.

PMID: 34146377 PMC: 8464298. DOI: 10.1002/vms3.555.


Developmental events and cellular changes occurred during esophageal development of quail embryos.

Soliman S, Madkour F Sci Rep. 2021; 11(1):7257.

PMID: 33790338 PMC: 8012389. DOI: 10.1038/s41598-021-86503-9.

References
1.
Spitz L, Ruangtrakool R . Esophageal substitution. Semin Pediatr Surg. 1998; 7(2):130-3. DOI: 10.1016/s1055-8586(98)70028-9. View

2.
Cusick E, Batchelor A, Spicer R . Development of a technique for jejunal interposition in long-gap esophageal atresia. J Pediatr Surg. 1993; 28(8):990-4. DOI: 10.1016/0022-3468(93)90499-b. View

3.
RAFFENSPERGER J, Luck S, Reynolds M, Schwartz D . Intestinal bypass of the esophagus. J Pediatr Surg. 1996; 31(1):38-46; discussion 46-7. DOI: 10.1016/s0022-3468(96)90316-4. View

4.
Spitz L . Esophageal atresia. Lessons I have learned in a 40-year experience. J Pediatr Surg. 2006; 41(10):1635-40. DOI: 10.1016/j.jpedsurg.2006.07.004. View

5.
Arul G, Parikh D . Oesophageal replacement in children. Ann R Coll Surg Engl. 2008; 90(1):7-12. PMC: 2216706. DOI: 10.1308/003588408X242222. View