Yi Zhou

Dr. Yi Zhou

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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1 August 2015 in Journal of Dentistry
Verified
Journal Article
Closed access
YWYining Wang
Yining Wang
JGJinxia Gao
Jinxia Gao
TJTao Jiang
Tao Jiang
SLShanshan Liang
Shanshan Liang
YZYi Zhou
Yi Zhou
BMBruce A. Matis
Bruce A. Matis

24 October 2024 in Acta Biomaterialia
Verified
Journal Article
Closed access
LHLin Huang
Lin Huang
TWTao Wu
Tao Wu
JSJing Sun
Jing Sun
XLXinghuan Lin
Xinghuan Lin
YPYuhao Peng
Yuhao Peng
BDBo Duan
Bo Duan

9 July 2019 in Journal of Clinical Periodontology
Verified
Journal Article
Closed access
PDF file
JHJing Huang
Jing Huang
XCXinjie Cai
Xinjie Cai
YOYanjing Ou
Yanjing Ou
LFLe Fan
Le Fan
YZYi Zhou
Yi Zhou
YWYining Wang
Yining Wang

2 October 2023 in Inflammation
Verified
Journal Article
Closed access
PDF file
DGDonghua Guo
Donghua Guo
WDWei Dong
Wei Dong
YCYaqi Cong
Yaqi Cong
YLYi Liu
Yi Liu
YLYoude Liang
Youde Liang
YZYi Zhou
Yi Zhou

9 October 2023 in Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
Verified
Journal Article
Closed access
JHJing Huang
Jing Huang
YWYining Wang
Yining Wang
YZYi Zhou
Yi Zhou

7 April 2022 in RSC Advances
Verified
Journal Article
Open access
PDF file
JHJing Huang
Jing Huang
YWYining Wang
Yining Wang
YZYi Zhou
Yi Zhou
Bone marrow-derived mesenchymal stem cells (BMSCs) are commonly used seed cells, and BMSC-derived primed cartilage templates have been shown to achieve bone regeneration in bone tissue engineering. Aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor involved in various cellular processes such as osteogenesis and immune regulation. This study investigated the effects of the AhR endogenous ligand 6-formyl (3,2-b) carbazole (FICZ) on the behavior of BMSCs and cartilage templates as well as the possible underlying molecular mechanisms. AhR expressions in rat bone marrow and isolated BMSCs were detected via immunohistochemistry (IHC) and immunofluorescent staining. Alkaline phosphatase staining and alizarin red staining showed that FICZ treatment enhanced the osteogenic potential of BMSCs without influencing their proliferation. FICZ was shown to alleviate the LPS-induced inflammatory cytokines IL-1β, 6 and TNF-α via the quantitative polymerase chain reaction (qPCR). In the chondrogenic process from BMSCs to primed cartilage templates, the expressions of AhR and its target gene cytochrome P450 subfamily B member 1 (CYP1B1) were inhibited. However, IHC staining demonstrated that AhR was still involved in the subcutaneous ossification of cartilage templates. Then, the effects of FICZ on cartilage templates were investigated. The osteogenic markers were upregulated by FICZ administration. The RAW 264.7 treated by condition medium of FICZ-treated cartilage templates exhibited an anti-inflammatory phenotype. Finally, high-throughput sequencing was applied to analyze the differentially expressed genes (DEGs) in the FICZ-treated cartilage templates. The upregulation of cytochrome P450 subfamily A member 1 (CYP1A1) and sphingomyelin phosphodiesterase 3 (Smpd3) were verified by qPCR, which might be the downstream targets of AhR in the cartilage templates promoting osteogenesis and macrophage polarization. These data implied a beneficial role of FICZ in the regenerative potentials of both BMSCs and primed cartilage templates. The FICZ/AhR axis might be a practical target to achieve optimal bone regeneration.