Metabolic degradation of polysaccharides from Lentinus edodes by Kupffer cells via the Dectin-1/Syk signaling pathway

被引:5
|
作者
Zhang, Yu [1 ,2 ]
Tang, Wenqi [1 ]
Zheng, Ziming [1 ,2 ]
Nie, Gang [3 ]
Zhan, Yuxue [1 ]
Mu, Xu [4 ]
Liu, Yuxuan [4 ]
Wang, Kaiping [4 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Pharm, Wuhan 430030, Peoples R China
[2] Hubei Prov Clin Res Ctr Precis Med Crit Illness, Wuhan 430030, Peoples R China
[3] Huazhong Univ Sci & Technol, Wuhan Childrens Hosp, Wuhan Maternal & Child Healthcare Hosp, Tongji Med Coll,Dept Pharm, Wuhan 430019, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Med Coll Pharm, Hubei Key Lab Nat Med Chem & Resource Evaluat, Wuhan 430030, Peoples R China
基金
中国国家自然科学基金;
关键词
Lentinan; Fluorescent labeling; Metabolic degradation; Dectin-1; Kupffer cells; BETA-GLUCAN RECEPTOR; HOST-DEFENSE; LIVER; GROWTH; INHIBITION; ACTIVATION; ROLES;
D O I
10.1016/j.carbpol.2023.121108
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
It had been shown that lentinan (LNT) was mainly distributed in the liver after intravenous administration. The study aimed to investigate the integrated metabolic processes and mechanisms of LNT in the liver, as these have not been thoroughly explored. In current work, 5-([4,6-dichlorotriazin-2-yl] amino) fluorescein and cyanine 7 were used to label LNT for tracking its metabolic behavior and mechanisms. Near-infrared imaging demonstrated that LNT was captured mainly by the liver. Kupffer cell (KC) depletion reduced LNT liver localization and degradation in BALB/c mice. Moreover, experiments with Dectin-1 siRNA and Dectin-1/Syk signaling pathway inhibitors showed that LNT was mainly taken up by KCs via the Dectin-1/Syk pathway and promoted lysosomal maturation in KCs via this same pathway, which in turn promoted LNT degradation. These empirical findings offer novel insights into the metabolism of LNT in vivo and in vitro, which will facilitate the further application of LNT and other & beta;-glucans.
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收藏
页数:14
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