» Articles » PMID: 10431784

Major Carbohydrate Epitopes in Tissues of Domestic and African Wild Animals of Potential Interest for Xenotransplantation Research

Overview
Specialty General Surgery
Date 1999 Oct 3
PMID 10431784
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

We investigated the main glycotopes expressed on the tissues of 44 animal species, including primates, nonprimate mammals, marsupials, birds, and a reptile. Paraffin-embedded tissue sections of kidney, heart, liver, pancreas, lung, brain and intestine of 24 domestic animal species were stained with seven fluorescent-labeled lectins. Testis sections of 20 African wild animal species were tested with the same lectins. Overall, three main immunofluorescence patterns were found in the vascular compartment. First, humans and Old World monkeys express genetically polymorphic ABH antigens and do not express alphaGal. Second, New World monkeys, other mammals, and marsupials do not express ABH antigens, but have large amounts of a genetically monomorphic alphaGal. Third, birds and reptiles do not express either ABH or alphaGal, but have monomorphic betaGal, probably different from the lactosamine precursor of ABH and alphaGal. Epithelial cells producing exocrine secretions also expressed carbohydrate epitopes. The fluorescence patterns of the cells of the exocrine compartment are similar, but not identical, to those expressed in the vascular compartment. All the animals tested have some ABH and betaGal in exocrine tissues, but New World monkeys and lower mammals are the only ones expressing alphaGal in exocrine tissues.

Citing Articles

Accelerated Burn Healing in a Mouse Experimental Model Using α-Gal Nanoparticles.

Galili U Bioengineering (Basel). 2023; 10(10).

PMID: 37892895 PMC: 10604883. DOI: 10.3390/bioengineering10101165.


Antibody production and tolerance to the α-gal epitope as models for understanding and preventing the immune response to incompatible ABO carbohydrate antigens and for α-gal therapies.

Galili U Front Mol Biosci. 2023; 10:1209974.

PMID: 37449060 PMC: 10338101. DOI: 10.3389/fmolb.2023.1209974.


α-Gal Nanoparticles Mediated Homing of Endogenous Stem Cells for Repair and Regeneration of External and Internal Injuries by Localized Complement Activation and Macrophage Recruitment.

Galili U, Goldufsky J, Schaer G Int J Mol Sci. 2022; 23(19).

PMID: 36232789 PMC: 9569695. DOI: 10.3390/ijms231911490.


Increasing Efficacy of Enveloped Whole-Virus Vaccines by In situ Immune-Complexing with the Natural Anti-Gal Antibody.

Galili U Med Res Arch. 2021; 9(7).

PMID: 34853815 PMC: 8631339. DOI: 10.18103/mra.v9i7.2481.


Biomanufacturing of Axon-Based Tissue Engineered Nerve Grafts Using Porcine GalSafe Neurons.

Katiyar K, Burrell J, Laimo F, Browne K, Bianchi J, Walters A Tissue Eng Part A. 2021; 27(19-20):1305-1320.

PMID: 33514288 PMC: 8610031. DOI: 10.1089/ten.TEA.2020.0303.