Structural characterization and immunoregulatory activity of a novel acidic polysaccharide from Scapharca subcrenata.

Acidic polysaccharide Scapharca subcrenata Structural characterization and immunoregulatory activity

Journal

International journal of biological macromolecules
ISSN: 1879-0003
Titre abrégé: Int J Biol Macromol
Pays: Netherlands
ID NLM: 7909578

Informations de publication

Date de publication:
15 Jun 2022
Historique:
received: 13 12 2021
revised: 01 04 2022
accepted: 27 04 2022
pubmed: 4 5 2022
medline: 1 6 2022
entrez: 3 5 2022
Statut: ppublish

Résumé

A novel acidic polysaccharide named SSPA50-1 was isolated from Scapharca subcrenata using a simulated gastric fluid extraction method. SSPA50-1 is a heteropolysaccharide with an average molecular weight of 44.7 kDa that is composed of galacturonic acid, glucose, galactose, mannose, ribose, rhamnose, fucose, xylose and arabinose at a molar ratio of 1.00:5.40:9.04:3.10:1.59:4.01:2.10:2.21:2.28. The structural characterization based on the methylation and 1D/2D NMR analyses indicated that SSPA50-1 is composed of →3)-β-L-Rhap-(1→, →3)-β-L-2-O-Me-Fucp-(1→, →2)-α-D-Xylp-(1→, →5)-α-L-Araf-(1→, →3)-β-D-Galp-(1→, →6)-α-D-Glcp-(1→, →3,4)-β-D-Manp-(1→, →3,4)-β-D-Galp-(1→, β-D-Ribf-(1→, α-D-Glcp-(1→, and α-D-GalAp6Me-(1→. Furthermore, SSPA50-1 possessed potent immunoregulatory activity by enhancing the phagocytosis and NO, iNOS, TNF-α and IL-6 secretion capacity of RAW264.7 cells. Otherwise, SSPA50-1 significantly promoted the proliferation of splenic lymphocytes and RAW264.7 macrophages. These results indicated that SSPA50-1 could be developed as a potential ingredient for immunostimulatory agents.

Identifiants

pubmed: 35504419
pii: S0141-8130(22)00924-2
doi: 10.1016/j.ijbiomac.2022.04.204
pii:
doi:

Substances chimiques

Polysaccharides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

439-454

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Hang Li (H)

Biotechnological Institute of Chinese Materia Medica, Jinan University, Guangzhou 510632, China.

Jianhuan Li (J)

Department of Pharmacology, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China.

Hui Shi (H)

Department of Natural Product Chemistry, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China; Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China.

Chunlei Li (C)

Biotechnological Institute of Chinese Materia Medica, Jinan University, Guangzhou 510632, China.

Weijuan Huang (W)

Department of Pharmacology, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China.

Man Zhang (M)

Department of Natural Product Chemistry, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China.

Yuanyuan Luo (Y)

Biotechnological Institute of Chinese Materia Medica, Jinan University, Guangzhou 510632, China.

Liyan Song (L)

Biotechnological Institute of Chinese Materia Medica, Jinan University, Guangzhou 510632, China; Department of Pharmacology, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China. Electronic address: tsly@jnu.edu.cn.

Rongmin Yu (R)

Biotechnological Institute of Chinese Materia Medica, Jinan University, Guangzhou 510632, China; Department of Natural Product Chemistry, Jinan University, 601 Huangpu Avenue West, Guangzhou 510632, China; Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China. Electronic address: tyrm@jnu.edu.cn.

Jianhua Zhu (J)

Biotechnological Institute of Chinese Materia Medica, Jinan University, Guangzhou 510632, China; Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China. Electronic address: tzhujh@jnu.edu.cn.

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Classifications MeSH