| Literature DB >> 33140917 |
Pierre Gillotay1, Meghna Shankar1, Benoit Haerlingen1, Eski Sema Elif1, Macarena Pozo-Morales1, Inés Garteizgogeascoa1, Susanne Reinhardt2, Annekathrin Kränkel2, Juliane Bläsche2, Andreas Petzold2, Nikolay Ninov3, Gokul Kesavan4, Christian Lange4, Michael Brand4, Anne Lefort4, Frédérick Libert4, Vincent Detours1, Sabine Costagliola1, Singh Sumeet Pal1.
Abstract
The thyroid gland regulates growth and metabolism via production of thyroid hormone in follicles composed of thyrocytes. So far, thyrocytes have been assumed to be a homogenous population. To uncover heterogeneity in the thyrocyte population and molecularly characterize the non-thyrocyte cells surrounding the follicle, we developed a single-cell transcriptome atlas of the region containing the zebrafish thyroid gland. The 6249-cell atlas includes profiles of thyrocytes, blood vessels, lymphatic vessels, immune cells, and fibroblasts. Further, the thyrocytes show expression heterogeneity, including bimodal expression of the transcription factor pax2a. To validate thyrocyte heterogeneity, we generated a CRISPR/Cas9-based pax2a knock-in line that monitors pax2a expression in the thyrocytes. A population of pax2a-low mature thyrocytes interspersed in individual follicles can be distinguished. We corroborate heterogeneity within the thyrocyte population using RNA sequencing of pax2a-high and pax2a-low thyrocytes, which demonstrates 20% differential expression in transcriptome between the two subpopulations. Our results identify and validate transcriptional differences within the presumed homogenous thyrocyte population.Entities:
Keywords: CRISPR/Cas9; heterogeneity; single-cell; thyroid gland; zebrafish
Mesh:
Year: 2020 PMID: 33140917 PMCID: PMC7726803 DOI: 10.15252/embr.202050612
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 9.071