Original article published by Cell Press on October 11, 2016. Click here to read the original article.

Highlights

• Mass cytometry promotes high-throughput phenotyping of islets at a single-cell level
• Alpha cells maintain higher basal proliferation and are more responsive to mitogens
• Beta cells exist in distinct states

Summary

The human endocrine pancreas consists of multiple cell types and plays a critical role in glucose homeostasis. Here, we apply mass cytometry technology to measure all major islet hormones, proliferative markers, and readouts of signaling pathways involved in proliferation at single-cell resolution. Using this innovative technology, we simultaneously examined baseline proliferation levels of all endocrine cell types from birth through adulthood, as well as in response to the mitogen harmine. High-dimensional analysis of our marker protein expression revealed three major clusters of beta cells within individuals. Proliferating beta cells are confined to two of the clusters.

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