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Abstract
Previous studies of bladder cell classification mostly relied on the cell’s morphology,
location, electrophysiology, and function. However, it is difficult to classify bladder
cells accurately and comprehensively using these methods. The authors created a single-cell
transcriptomic map of human bladder cells using single-cell RNA sequencing. They also
created a more detailed single-cell sequencing RNA map of the mouse bladder than what
was previously available. Using these tools, the authors compare the similarities
and differences between human and mouse bladder cells and found many cell types that
are highly similar across the two. Additionally, the authors discovered two new types
of human bladder cells. One may play a role in allergic reactions and nerve conduction,
whereas the other may play a role in bladder emptying. The results may assist scientists
studying the relationship between bladder cell types and diseases. Having a comprehensive
map of the cellular anatomy of the normal human bladder is vital to understanding
the cellular origins of benign bladder disease and bladder cancer. We used single-cell
RNA sequencing (scRNA-seq) of 12,423 cells from healthy human bladder tissue samples
taken from patients with bladder cancer and 12,884 cells from mouse bladders to classify
bladder cell types and their underlying functions. We created a single-cell transcriptomic
map of human and mouse bladders, including 16 clusters of human bladder cells and
15 clusters of mouse bladder cells. The homology and heterogeneity of human and mouse
bladder cell types were compared and both conservative and heterogeneous aspects of
human and mouse bladder evolution were identified. We also discovered two novel types
of human bladder cells. One type is ADRA2A + and HRH2 + interstitial cells which
may be associated with nerve conduction and allergic reactions. The other type is
TNNT1 + epithelial cells that may be involved with bladder emptying. We verify these
TNNT1 + epithelial cells also occur in rat and mouse bladders. This transcriptomic
map provides a resource for studying bladder cell types, specific cell markers, signaling
receptors, and genes that will help us to learn more about the relationship between
bladder cell types and diseases.
Understanding tumor origins and the similarities and differences between organ-specific cancers is important for determining treatment options. Young et al. generated more than 72,000 single-cell transcriptomes from healthy and cancerous human kidneys. From these data, they determined that Wilms tumor, a pediatric kidney cancer, originates from aberrant fetal cells, whereas adult kidney cancers are likely derived from a specific subtype of proximal convoluted tubular cell. Science , this issue p. [Related article:] 594 Single-cell mRNAs of normal and cancerous kidney cells reveal the cellular identity of childhood and adult tumors. Messenger RNA encodes cellular function and phenotype. In the context of human cancer, it defines the identities of malignant cells and the diversity of tumor tissue. We studied 72,501 single-cell transcriptomes of human renal tumors and normal tissue from fetal, pediatric, and adult kidneys. We matched childhood Wilms tumor with specific fetal cell types, thus providing evidence for the hypothesis that Wilms tumor cells are aberrant fetal cells. In adult renal cell carcinoma, we identified a canonical cancer transcriptome that matched a little-known subtype of proximal convoluted tubular cell. Analyses of the tumor composition defined cancer-associated normal cells and delineated a complex vascular endothelial growth factor (VEGF) signaling circuit. Our findings reveal the precise cellular identities and compositions of human kidney tumors.
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