PT - JOURNAL ARTICLE AU - Chai, Xiaoqiang AU - Hu, Longfei AU - Zhang, Yan AU - Han, Weiyu AU - Lu, Zhou AU - Ke, Aiwu AU - Zhou, Jian AU - Shi, Guoming AU - Fang, Nan AU - Fan, Jia AU - Cai, Jiabin AU - Fan, Jue AU - Lan, Fei TI - Specific ACE2 Expression in Cholangiocytes May Cause Liver Damage After 2019-nCoV Infection AID - 10.1101/2020.02.03.931766 DP - 2020 Jan 01 TA - bioRxiv PG - 2020.02.03.931766 4099 - http://biorxiv.org/content/early/2020/02/04/2020.02.03.931766.short 4100 - http://biorxiv.org/content/early/2020/02/04/2020.02.03.931766.full AB - A newly identified coronavirus, 2019-nCoV, has been posing significant threats to public health since December 2019. ACE2, the host cell receptor for severe acute respiratory syndrome coronavirus (SARS), has recently been demonstrated in mediating 2019-nCoV infection. Interestingly, besides the respiratory system, substantial proportion of SARS and 2019-nCoV patients showed signs of various degrees of liver damage, the mechanism and implication of which have not yet been determined. Here, we performed an unbiased evaluation of cell type specific expression of ACE2 in healthy liver tissues using single cell RNA-seq data of two independent cohorts, and identified specific expression in cholangiocytes. The results indicated that virus might directly bind to ACE2 positive cholangiocytes but not necessarily hepatocytes. This finding suggested the liver abnormalities of SARS and 2019-nCoV patients may not be due to hepatocyte damage, but cholangiocyte dysfunction and other causes such as drug induced and systemic inflammatory response induced liver injury. Our findings indicate that special care of liver dysfunction should be installed in treating 2019-nCoV patients during the hospitalization and shortly after cure.