Journal
ASIAN JOURNAL OF ANDROLOGY
Volume 25, Issue 1, Pages 103-112Publisher
WOLTERS KLUWER MEDKNOW PUBLICATIONS
DOI: 10.4103/aja202226
Keywords
disorders of sex development; human epididymis; NR5A1; scRNA-seq
Categories
Ask authors/readers for more resources
This study characterized the cell atlas of the epididymis in a 46,XY disorders of sex development patient with a novel heterozygous mutation in the NR5A1 gene. The patient exhibited feminization of external genitalia and dysplastic testis. Single-cell RNA sequencing analysis revealed an increase in fibroblast cells and a decrease in main epididymal epithelial cells, suggesting an association with the epithelial-to-mesenchymal transition process. This study provides important insights into the pathophysiology of DSD.
This study aims to characterize the cell atlas of the epididymis derived from a 46,XY disorders of sex development (DSD) patient with a novel heterozygous mutation of the nuclear receptor subfamily 5 group A member 1 (NR5A1) gene. Next-generation sequencing found a heterozygous c.124C > G mutation in NR5A1 that resulted in a p.Q42E missense mutation in the conserved DNA-binding domain of NR5A1. The patient demonstrated feminization of external genitalia and Tanner stage 1 breast development. The surgical procedure revealed a morphologically normal epididymis and vas deferens but a dysplastic testis. Microfluidic-based single-cell RNA sequencing (scRNA-seq) analysis found that the fibroblast cells were significantly increased (approximately 46.5%), whereas the number of main epididymal epithelial cells (approximately 9.2%), such as principal cells and basal cells, was dramatically decreased. Bioinformatics analysis of cell-cell communications and gene regulatory networks at the single-cell level inferred that epididymal epithelial cell loss and fibroblast occupation are associated with the epithelial-to-mesenchymal transition (EMT) process. The present study provides a cell atlas of the epididymis of a patient with 46,XY DSD and serves as an important resource for understanding the pathophysiology of DSD.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available