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A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells

In this study, a novel heteropolysaccharide (ASPA80-1) with an average molecular weight of 5.48 × 10(4) Da was isolated and structurally elucidated from custard apple pulp (Annona squamosa) through DEAE-cellulose, Sephadex G-100 and Sephacryl S-300 HR chromatography and spectral analysis. ASPA80-1 i...

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Autores principales: Huang, Chunhua, Tu, Wensong, Zhang, Man, Peng, Dan, Guo, Zhongyi, Huang, Weijuan, Zhu, Jianhua, Yu, Rongmin, Song, Liyan, Wang, Yurong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404978/
https://www.ncbi.nlm.nih.gov/pubmed/37554813
http://dx.doi.org/10.1016/j.heliyon.2023.e18521
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author Huang, Chunhua
Tu, Wensong
Zhang, Man
Peng, Dan
Guo, Zhongyi
Huang, Weijuan
Zhu, Jianhua
Yu, Rongmin
Song, Liyan
Wang, Yurong
author_facet Huang, Chunhua
Tu, Wensong
Zhang, Man
Peng, Dan
Guo, Zhongyi
Huang, Weijuan
Zhu, Jianhua
Yu, Rongmin
Song, Liyan
Wang, Yurong
author_sort Huang, Chunhua
collection PubMed
description In this study, a novel heteropolysaccharide (ASPA80-1) with an average molecular weight of 5.48 × 10(4) Da was isolated and structurally elucidated from custard apple pulp (Annona squamosa) through DEAE-cellulose, Sephadex G-100 and Sephacryl S-300 HR chromatography and spectral analysis. ASPA80-1 is a water-soluble polysaccharide and it is a polymer consisting of predominant amounts of (1 → 3)-linked-L-arabinose (Ara) residues, small amounts of (1 → 6)-linked-D-galactose (Gal), (1 → 3,5)-linked-L-arabinose (Ara) residues and terminal linked-L-arabinose (Ara) residues, trace amount of (1 → 4)-linked-D-glucose (Glc) residues and (1 → 2)-linked-L-rhamnose (Rham) residues. ASPA80-1 showed significant effect on antigen-presenting cells (APCs) activation. On the one hand, ASPA80-1 activated RAW264.7 macrophage cells by inducing morphology change, enhancing phagocytic ability, increasing nitric oxide (NO) secretion and promoting expression of major histocompatibility complex class II (MHC II) and cluster of differentiation 86 (CD 86). On the other hand, ASPA80-1 promoted the maturation of dendritic cells (DCs) by inducing longer dendrites, decreasing phagocytic ability and increasing MHC II and CD86 expression. Furthermore, mitogen-activated protein kinases (MAPKs) and nuclear factor kappa B (NF-κB) signaling pathways were activated after the intervention of ASPA80-1 on RAW264.7 cells or DCs. Thus, the novel heteropolysaccharide ASPA80-1 has the potential to be used as an immunoenhancing component in functional foods.
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spelling pubmed-104049782023-08-08 A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells Huang, Chunhua Tu, Wensong Zhang, Man Peng, Dan Guo, Zhongyi Huang, Weijuan Zhu, Jianhua Yu, Rongmin Song, Liyan Wang, Yurong Heliyon Research Article In this study, a novel heteropolysaccharide (ASPA80-1) with an average molecular weight of 5.48 × 10(4) Da was isolated and structurally elucidated from custard apple pulp (Annona squamosa) through DEAE-cellulose, Sephadex G-100 and Sephacryl S-300 HR chromatography and spectral analysis. ASPA80-1 is a water-soluble polysaccharide and it is a polymer consisting of predominant amounts of (1 → 3)-linked-L-arabinose (Ara) residues, small amounts of (1 → 6)-linked-D-galactose (Gal), (1 → 3,5)-linked-L-arabinose (Ara) residues and terminal linked-L-arabinose (Ara) residues, trace amount of (1 → 4)-linked-D-glucose (Glc) residues and (1 → 2)-linked-L-rhamnose (Rham) residues. ASPA80-1 showed significant effect on antigen-presenting cells (APCs) activation. On the one hand, ASPA80-1 activated RAW264.7 macrophage cells by inducing morphology change, enhancing phagocytic ability, increasing nitric oxide (NO) secretion and promoting expression of major histocompatibility complex class II (MHC II) and cluster of differentiation 86 (CD 86). On the other hand, ASPA80-1 promoted the maturation of dendritic cells (DCs) by inducing longer dendrites, decreasing phagocytic ability and increasing MHC II and CD86 expression. Furthermore, mitogen-activated protein kinases (MAPKs) and nuclear factor kappa B (NF-κB) signaling pathways were activated after the intervention of ASPA80-1 on RAW264.7 cells or DCs. Thus, the novel heteropolysaccharide ASPA80-1 has the potential to be used as an immunoenhancing component in functional foods. Elsevier 2023-07-23 /pmc/articles/PMC10404978/ /pubmed/37554813 http://dx.doi.org/10.1016/j.heliyon.2023.e18521 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Huang, Chunhua
Tu, Wensong
Zhang, Man
Peng, Dan
Guo, Zhongyi
Huang, Weijuan
Zhu, Jianhua
Yu, Rongmin
Song, Liyan
Wang, Yurong
A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells
title A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells
title_full A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells
title_fullStr A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells
title_full_unstemmed A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells
title_short A novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells
title_sort novel heteropolysaccharide isolated from custard apple pulp and its immunomodulatory activity in mouse macrophages and dendritic cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404978/
https://www.ncbi.nlm.nih.gov/pubmed/37554813
http://dx.doi.org/10.1016/j.heliyon.2023.e18521
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