Xindi Shan

Dr. Xindi Shan

Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma, USA
orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

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

Representative Publications

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23 October 2020 in Science
Verified
Journal Article
Closed access
KBKirk Bergstrom
Kirk Bergstrom
XSXindi Shan
Xindi Shan
DCDavid Casero
David Casero
ABAlbert Batushansky
Albert Batushansky
VLVenu Lagishetty
Venu Lagishetty
LXLijun Xia
Lijun Xia
So much more to mucus: Mammals accommodate a dense community of metabolically active microorganisms in their gut. This is not a passive relationship, and host and microbe have antagonistic as well as mutualistic responses to each other. Using a whole-colon imaging method in mice, Bergstrom et al. looked at the role of colonic mucus in segregating the microbiota from host cells during elimination of feces (see the Perspective by Birchenough and Johansson). Host goblet cells synthesize two forms of mucin that differ in branched chain O-glycosylation and the site of production in the colon. A “thick” mucus in the proximal, ascending colon wraps the microbiota to form fecal pellets. Transit along the distal, descending colon is lubricated by “thin” mucus that transiently links with the thick mucus. Normal mucus encapsulation prevents inflammation and hyperplasia and thus is important for maintenance of a healthy gut. Science , this issue p. 467 ; see also p. 402

1 February 2017 in Carbohydrate Polymers
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Journal Article
Closed access
LDLang Ding
Lang Ding
XSXindi Shan
Xindi Shan
XZXiaoliang Zhao
Xiaoliang Zhao
HZHualian Zha
Hualian Zha
XCXiaoyu Chen
Xiaoyu Chen
Guangli YuGuangli Yu
Guangli Yu

1 September 2017 in Toxicology Letters
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Journal Article
Closed access
Qingsen ShangQingsen Shang
Qingsen Shang
WSWeixia Sun
Weixia Sun
XSXindi Shan
Xindi Shan
HJHao Jiang
Hao Jiang
CCChao Cai
Chao Cai
Guangli YuGuangli Yu
Guangli Yu

1 January 2016 in International Journal of Biological Macromolecules
Verified
Journal Article
Closed access
XSXindi Shan
Xindi Shan
XLXin Liu
Xin Liu
JHJiejie Hao
Jiejie Hao
CCChao Cai
Chao Cai
FFFei Fan
Fei Fan
Guangli YuGuangli Yu
Guangli Yu

17 January 2017 in Scientific Reports
Verified
Journal Article
Open access
Wei WangWei Wang
Wei Wang
JWJiandong Wu
Jiandong Wu
XZXiaoshuang Zhang
Xiaoshuang Zhang
CHCui Hao
Cui Hao
XZXiaoliang Zhao
Xiaoliang Zhao
Guangli YuGuangli Yu
Guangli Yu
Development of novel anti-influenza A virus (IAV) drugs with high efficiency and low toxicity is critical for preparedness against influenza outbreaks. Herein, we investigated the anti-IAV activities and mechanisms of fucoidan in vitro and in vivo. The results showed that a fucoidan KW derived from brown algae Kjellmaniella crassifolia effectively blocked IAV infection in vitro with low toxicity. KW possessed broad anti-IAV spectrum and low tendency of induction of viral resistance, superior to the anti-IAV drug amantadine. KW was capable of inactivating virus particles before infection and blocked some stages after adsorption. KW could bind to viral neuraminidase (NA) and inhibit the activity of NA to block the release of IAV. KW also interfered with the activation of EGFR, PKCα, NF-κB, and Akt, and inhibited both IAV endocytosis and EGFR internalization in IAV-infected cells, suggesting that KW may also inhibit cellular EGFR pathway. Moreover, intranasal administration of KW markedly improved survival and decreased viral titers in IAV-infected mice. Therefore, fucoidan KW has the potential to be developed into a novel nasal drop or spray for prevention and treatment of influenza in the future.

26 November 2018 in Cell Death & Differentiation
Verified
Journal Article
Closed access
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JYJun Yi
Jun Yi
KBKirk Bergstrom
Kirk Bergstrom
JFJianxin Fu
Jianxin Fu
XSXindi Shan
Xindi Shan
JMJ. Michael McDaniel
J. Michael McDaniel
LXLijun Xia
Lijun Xia