A spatiotemporal atlas of mouse liver homeostasis and regeneration
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A spatiotemporal atlas of mouse liver homeostasis and regeneration. / Xu, Jiangshan; Guo, Pengcheng; Hao, Shijie; Shangguan, Shuncheng; Shi, Quan; Volpe, Giacomo; Huang, Keke; Zuo, Jing; An, Juan; Yuan, Yue; Cheng, Mengnan; Deng, Qiuting; Zhang, Xiao; Lai, Guangyao; Nan, Haitao; Wu, Baihua; Shentu, Xinyi; Wu, Liang; Wei, Xiaoyu; Jiang, Yujia; Huang, Xin; Pan, Fengyu; Song, Yumo; Li, Ronghai; Wang, Zhifeng; Liu, Chuanyu; Liu, Shiping; Li, Yuxiang; Yang, Tao; Xu, Zhicheng; Du, Wensi; Li, Ling; Ahmed, Tanveer; You, Kai; Dai, Zhen; Li, Li; Qin, Baoming; Li, Yinxiong; Lai, Liangxue; Qin, Dajiang; Chen, Junling; Fan, Rong; Li, Yongyin; Hou, Jinlin; Ott, Michael; Sharma, Amar Deep; Cantz, Tobias; Schambach, Axel; Kristiansen, Karsten; Hutchins, Andrew P.; Göttgens, Berthold; Maxwell, Patrick H.; Hui, Lijian; Xu, Xun; Liu, Longqi; Chen, Ao; Lai, Yiwei; Esteban, Miguel A.
In: Nature Genetics, Vol. 56, 2024, p. 953-969.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - A spatiotemporal atlas of mouse liver homeostasis and regeneration
AU - Xu, Jiangshan
AU - Guo, Pengcheng
AU - Hao, Shijie
AU - Shangguan, Shuncheng
AU - Shi, Quan
AU - Volpe, Giacomo
AU - Huang, Keke
AU - Zuo, Jing
AU - An, Juan
AU - Yuan, Yue
AU - Cheng, Mengnan
AU - Deng, Qiuting
AU - Zhang, Xiao
AU - Lai, Guangyao
AU - Nan, Haitao
AU - Wu, Baihua
AU - Shentu, Xinyi
AU - Wu, Liang
AU - Wei, Xiaoyu
AU - Jiang, Yujia
AU - Huang, Xin
AU - Pan, Fengyu
AU - Song, Yumo
AU - Li, Ronghai
AU - Wang, Zhifeng
AU - Liu, Chuanyu
AU - Liu, Shiping
AU - Li, Yuxiang
AU - Yang, Tao
AU - Xu, Zhicheng
AU - Du, Wensi
AU - Li, Ling
AU - Ahmed, Tanveer
AU - You, Kai
AU - Dai, Zhen
AU - Li, Li
AU - Qin, Baoming
AU - Li, Yinxiong
AU - Lai, Liangxue
AU - Qin, Dajiang
AU - Chen, Junling
AU - Fan, Rong
AU - Li, Yongyin
AU - Hou, Jinlin
AU - Ott, Michael
AU - Sharma, Amar Deep
AU - Cantz, Tobias
AU - Schambach, Axel
AU - Kristiansen, Karsten
AU - Hutchins, Andrew P.
AU - Göttgens, Berthold
AU - Maxwell, Patrick H.
AU - Hui, Lijian
AU - Xu, Xun
AU - Liu, Longqi
AU - Chen, Ao
AU - Lai, Yiwei
AU - Esteban, Miguel A.
N1 - Publisher Copyright: © The Author(s), under exclusive licence to Springer Nature America, Inc. 2024.
PY - 2024
Y1 - 2024
N2 - The mechanism by which mammalian liver cell responses are coordinated during tissue homeostasis and perturbation is poorly understood, representing a major obstacle in our understanding of many diseases. This knowledge gap is caused by the difficulty involved with studying multiple cell types in different states and locations, particularly when these are transient. We have combined Stereo-seq (spatiotemporal enhanced resolution omics-sequencing) with single-cell transcriptomic profiling of 473,290 cells to generate a high-definition spatiotemporal atlas of mouse liver homeostasis and regeneration at the whole-lobe scale. Our integrative study dissects in detail the molecular gradients controlling liver cell function, systematically defining how gene networks are dynamically modulated through intercellular communication to promote regeneration. Among other important regulators, we identified the transcriptional cofactor TBL1XR1 as a rheostat linking inflammation to Wnt/β-catenin signaling for facilitating hepatocyte proliferation. Our data and analytical pipelines lay the foundation for future high-definition tissue-scale atlases of organ physiology and malfunction.
AB - The mechanism by which mammalian liver cell responses are coordinated during tissue homeostasis and perturbation is poorly understood, representing a major obstacle in our understanding of many diseases. This knowledge gap is caused by the difficulty involved with studying multiple cell types in different states and locations, particularly when these are transient. We have combined Stereo-seq (spatiotemporal enhanced resolution omics-sequencing) with single-cell transcriptomic profiling of 473,290 cells to generate a high-definition spatiotemporal atlas of mouse liver homeostasis and regeneration at the whole-lobe scale. Our integrative study dissects in detail the molecular gradients controlling liver cell function, systematically defining how gene networks are dynamically modulated through intercellular communication to promote regeneration. Among other important regulators, we identified the transcriptional cofactor TBL1XR1 as a rheostat linking inflammation to Wnt/β-catenin signaling for facilitating hepatocyte proliferation. Our data and analytical pipelines lay the foundation for future high-definition tissue-scale atlases of organ physiology and malfunction.
U2 - 10.1038/s41588-024-01709-7
DO - 10.1038/s41588-024-01709-7
M3 - Journal article
C2 - 38627598
AN - SCOPUS:85190697199
VL - 56
SP - 953
EP - 969
JO - Nature Genetics
JF - Nature Genetics
SN - 1061-4036
ER -
ID: 391160870