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Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity

We examined whether deficiency of the GGTA1 gene in pigs altered the expression of several glycosyltransferase genes. Real-time RT-PCR and glycosyltransferase activity showed that 2 sialyltransferases [α2,3-sialyltransferase (α2,3ST) and α2,6-sialyltransferase (α2,6ST)] in the heterozygote GalT KO l...

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Autores principales: Park, Jong-Yi, Park, Mi-Ryung, Kwon, Deug-Nam, Kang, Min-Hui, Oh, Mihye, Han, Jae-Woong, Cho, Ssang-Goo, Park, Chankyu, Kim, Dong-Ku, Song, Hyuk, Oh, Jae-Wook, Kim, Jin-Hoi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205825/
https://www.ncbi.nlm.nih.gov/pubmed/22131812
http://dx.doi.org/10.1155/2011/560850
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author Park, Jong-Yi
Park, Mi-Ryung
Kwon, Deug-Nam
Kang, Min-Hui
Oh, Mihye
Han, Jae-Woong
Cho, Ssang-Goo
Park, Chankyu
Kim, Dong-Ku
Song, Hyuk
Oh, Jae-Wook
Kim, Jin-Hoi
author_facet Park, Jong-Yi
Park, Mi-Ryung
Kwon, Deug-Nam
Kang, Min-Hui
Oh, Mihye
Han, Jae-Woong
Cho, Ssang-Goo
Park, Chankyu
Kim, Dong-Ku
Song, Hyuk
Oh, Jae-Wook
Kim, Jin-Hoi
author_sort Park, Jong-Yi
collection PubMed
description We examined whether deficiency of the GGTA1 gene in pigs altered the expression of several glycosyltransferase genes. Real-time RT-PCR and glycosyltransferase activity showed that 2 sialyltransferases [α2,3-sialyltransferase (α2,3ST) and α2,6-sialyltransferase (α2,6ST)] in the heterozygote GalT KO liver have higher expression levels and activities compared to controls. Enzyme-linked lectin assays indicated that there were also more sialic acid-containing glycoconjugate epitopes in GalT KO livers than in controls. The elevated level of sialic-acid-containing glycoconjugate epitopes was due to the low level of α-Gal in heterozygote GalT KO livers. Furthermore, proteomics analysis showed that heterozygote GalT KO pigs had a higher expression of NAD(+)-isocitrate dehydrogenase (IDH), which is related to the CMP-N-acetylneuraminic acid hydroxylase (CMAH) enzyme reaction. These findings suggest the deficiency of GGTA1 gene in pigs results in increased production of N-glycolylneuraminic acid (Neu5Gc) due to an increase of α2,6-sialyltransferase and a CMAH cofactor, NAD(+)-IDH. This indicates that Neu5Gc may be a critical xenoantigen. The deletion of the CMAH gene in the GalT KO background is expected to further prolong xenograft survival.
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spelling pubmed-32058252011-11-30 Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity Park, Jong-Yi Park, Mi-Ryung Kwon, Deug-Nam Kang, Min-Hui Oh, Mihye Han, Jae-Woong Cho, Ssang-Goo Park, Chankyu Kim, Dong-Ku Song, Hyuk Oh, Jae-Wook Kim, Jin-Hoi J Biomed Biotechnol Research Article We examined whether deficiency of the GGTA1 gene in pigs altered the expression of several glycosyltransferase genes. Real-time RT-PCR and glycosyltransferase activity showed that 2 sialyltransferases [α2,3-sialyltransferase (α2,3ST) and α2,6-sialyltransferase (α2,6ST)] in the heterozygote GalT KO liver have higher expression levels and activities compared to controls. Enzyme-linked lectin assays indicated that there were also more sialic acid-containing glycoconjugate epitopes in GalT KO livers than in controls. The elevated level of sialic-acid-containing glycoconjugate epitopes was due to the low level of α-Gal in heterozygote GalT KO livers. Furthermore, proteomics analysis showed that heterozygote GalT KO pigs had a higher expression of NAD(+)-isocitrate dehydrogenase (IDH), which is related to the CMP-N-acetylneuraminic acid hydroxylase (CMAH) enzyme reaction. These findings suggest the deficiency of GGTA1 gene in pigs results in increased production of N-glycolylneuraminic acid (Neu5Gc) due to an increase of α2,6-sialyltransferase and a CMAH cofactor, NAD(+)-IDH. This indicates that Neu5Gc may be a critical xenoantigen. The deletion of the CMAH gene in the GalT KO background is expected to further prolong xenograft survival. Hindawi Publishing Corporation 2011 2011-10-25 /pmc/articles/PMC3205825/ /pubmed/22131812 http://dx.doi.org/10.1155/2011/560850 Text en Copyright © 2011 Jong-Yi Park et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Park, Jong-Yi
Park, Mi-Ryung
Kwon, Deug-Nam
Kang, Min-Hui
Oh, Mihye
Han, Jae-Woong
Cho, Ssang-Goo
Park, Chankyu
Kim, Dong-Ku
Song, Hyuk
Oh, Jae-Wook
Kim, Jin-Hoi
Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity
title Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity
title_full Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity
title_fullStr Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity
title_full_unstemmed Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity
title_short Alpha 1,3-Galactosyltransferase Deficiency in Pigs Increases Sialyltransferase Activities That Potentially Raise Non-Gal Xenoantigenicity
title_sort alpha 1,3-galactosyltransferase deficiency in pigs increases sialyltransferase activities that potentially raise non-gal xenoantigenicity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3205825/
https://www.ncbi.nlm.nih.gov/pubmed/22131812
http://dx.doi.org/10.1155/2011/560850
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