Xiaoqiang Han

Dr. Xiaoqiang Han


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2017 in Journal of Ethnopharmacology
Verified
Journal Article
Closed access
QZQiang Zeng
Qiang Zeng
CKChun-Hay Ko
Chun-Hay Ko
WSWing Sum Siu
Wing Sum Siu
LLLong-Fei Li
Long-Fei Li
XHXiaoqiang Han
Xiaoqiang Han
PLPing-Chung Leung
Ping-Chung Leung

23 August 2019 in PLOS ONE
Verified
Journal Article
Open access
PDF file
KLKaisheng Liu
Kaisheng Liu
CZCheng Zhang
Cheng Zhang
HDHong-Liang Dong
Hong-Liang Dong
KLKai-Kai Li
Kai-Kai Li
QHQuan-Bin Han
Quan-Bin Han
XHXiaoqiang Han
Xiaoqiang Han
Ganoderma sinense is a Chinese unique medicinal fungus that has been used in folk medicine for thousands of years. Polysaccharides are considered to be biologically active ingredients due to their immune-modulating functions. Previously we found that GSP-2, a new polysaccharide isolated from Ganoderma sinense, exerts an immunomodulatory effect in human peripheral blood mononuclear cells but the underlying mechanism is unclear. The present study aimed to investigate how GSP-2 triggers immunologic responses and the implicated signaling pathways. GSP-2 effects were investigated both in a macrophagic cell line, RAW264.7, and in primary macrophages. Moreover, the molecular basis of GSP-2 recognition by immune cells, and the consequent activation of signaling cascades, were explored by employing recombinant human HEK293-TLR-Blue clones, individually overexpressing various Toll-like receptors. GSP-2 dose-dependently induced the overexpression of Toll-like receptor 4 (TLR4) but did not affect the expression of other TLRs. Moreover, GSP-2 induced TNFα secretion in primary macrophages from wild-type, but not TLR4-knockout mice. In addition, GSP-2 upregulated TLR4 protein expression and activated the MAPK pathway in RAW246.7 macrophages. Finally, GSP-2 induced the production of the cytokines TNFα, IL1β, and IL6. Our data demonstrated that GSP-2 was specifically recognized by TLR4, promoting cytokine secretion and immune modulation in macrophages.