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?:abstract
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Background: Since December 2019, the novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), first spread quickly in Wuhan, China, then globally Based on previously published evidence, ACE2 and TMPRSS2 are both pivotal entry molecules that enable cellular infection by SARS-CoV-2 Also, increased expression of pro-inflammatory cytokines, or a \'cytokine storm,\' is associated with multiple organ dysfunction syndrome often observed in critically ill patients Methods: We investigated the expression pattern of ACE2 and TMPRSS2 in major organs in the human body, especially in specific disease conditions Multiple sequence alignment of ACE2 in different species was used to explain animal susceptibility Moreover, the cell-specific expression patterns of ACE2 and cytokine receptors in the urinary tract were assessed using single-cell RNA sequencing (scRNA-seq) Additional biological relevance was determined through Gene Set Enrichment Analysis (GSEA) using an ACE2-specific signature Results: Our results revealed that ACE2 and TMPRSS2 were highly expressed in genitourinary organs ACE2 was highly and significantly expressed in the kidney among individuals with chronic kidney diseases or diabetic nephropathy In single cells, ACE2 was primarily enriched in gametocytes in the testis and renal proximal tubules The receptors for pro-inflammatory cytokines, especially IL6ST, were notably concentrated in endothelial cells, macrophages, spermatogonial stem cells in the testis, and renal endothelial cells, which suggested the occurrence of alternative damaging autoimmune mechanisms Conclusion: This study provided new insights into the pathogenic mechanisms of SARS-CoV-2 that underlie the clinical manifestations observed in the human testis and kidney These observations might substantially facilitate the development of effective treatments for this rapidly spreading disease
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