Author
Listed:
- Weiwei Liang
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University
Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute at Frederick)
- Xinjian Peng
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
- Qingqing Li
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
- Pingzhang Wang
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
- Ping Lv
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
- Quansheng Song
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
- Shaoping She
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
- Shiyang Huang
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
- Keqiang Chen
(Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute at Frederick)
- Wanghua Gong
(Basic Research Program, Leidos Biomedical Research, Inc)
- Wuxing Yuan
(Microbiome Sequencing Core, Leidos Biomedical Research, Inc)
- Vishal Thovarai
(Basic Science Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research)
- Teizo Yoshimura
(Okayama University)
- Colm O’huigin
(Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute at Frederick)
- Giorgio Trinchieri
(Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute at Frederick)
- Jiaqiang Huang
(Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute at Frederick
Cancer Research Center, Beijing Chest Hospital affiliated to Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute)
- Shuye Lin
(Cancer Research Center, Beijing Chest Hospital affiliated to Capital Medical University, Beijing Tuberculosis & Thoracic Tumor Research Institute)
- Xiaohong Yao
(Institute of Pathology, South-west Hospital and Cancer Center)
- Xiuwu Bian
(Institute of Pathology, South-west Hospital and Cancer Center)
- Wei Kong
(Peking University)
- Jianzhong Xi
(Peking University)
- Ji Ming Wang
(Cancer and Inflammation Program, Center for Cancer Research, National Cancer Institute at Frederick)
- Ying Wang
(School of Basic Medical Sciences and NHC Key Laboratory of Medical Immunology, Peking University)
Abstract
The physiological homeostasis of gut mucosal barrier is maintained by both genetic and environmental factors and its impairment leads to pathogenesis such as inflammatory bowel disease. A cytokine like molecule, FAM3D (mouse Fam3D), is highly expressed in mouse gastrointestinal tract. Here, we demonstrate that deficiency in Fam3D is associated with impaired integrity of colonic mucosa, increased epithelial hyper-proliferation, reduced anti-microbial peptide production and increased sensitivity to chemically induced colitis associated with high incidence of cancer. Pretreatment of Fam3D−/− mice with antibiotics significantly reduces the severity of chemically induced colitis and wild type (WT) mice co-housed with Fam3D−/− mice phenocopy Fam3D-deficiency showing increased sensitivity to colitis and skewed composition of fecal microbiota. An initial equilibrium of microbiota in cohoused WT and Fam3D−/− mice is followed by an increasing divergence of the bacterial composition after separation. These results demonstrate the essential role of Fam3D in colon homeostasis, protection against inflammation associated cancer and normal microbiota composition.
Suggested Citation
Weiwei Liang & Xinjian Peng & Qingqing Li & Pingzhang Wang & Ping Lv & Quansheng Song & Shaoping She & Shiyang Huang & Keqiang Chen & Wanghua Gong & Wuxing Yuan & Vishal Thovarai & Teizo Yoshimura & C, 2020.
"FAM3D is essential for colon homeostasis and host defense against inflammation associated carcinogenesis,"
Nature Communications, Nature, vol. 11(1), pages 1-16, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19691-z
DOI: 10.1038/s41467-020-19691-z
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Cited by:
- Molly Went & Amit Sud & Charlie Mills & Abi Hyde & Richard Culliford & Philip Law & Jayaram Vijayakrishnan & Ines Gockel & Carlo Maj & Johannes Schumacher & Claire Palles & Martin Kaiser & Richard Hou, 2024.
"Phenome-wide Mendelian randomisation analysis of 378,142 cases reveals risk factors for eight common cancers,"
Nature Communications, Nature, vol. 15(1), pages 1-12, December.
- Xiaolei Pei & Li Liu & Jieru Wang & Changyuan Guo & Qingqing Li & Jia Li & Qian Ren & Runzhi Ma & Yi Zheng & Yan Zhang & Li Liu & Danfeng Zheng & Pingzhang Wang & Ping Jiang & Xiaoming Feng & Erlie Ji, 2024.
"Exosomal secreted SCIMP regulates communication between macrophages and neutrophils in pneumonia,"
Nature Communications, Nature, vol. 15(1), pages 1-17, December.
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