Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. A transcriptomic atlas of mouse cerebellar cortex comprehensively defines cell types

A transcriptomic atlas of mouse cerebellar cortex comprehensively defines cell types

Thumbnail Image
Download
Name

s41586-021-03220-z.pdf

Description
Published version
Size

15.08 MB

Format

Adobe PDF

Checksum (MD5)

74191d5716e914e5360be85bb01771d3

sword-2023-01-13T13:52:20.original.xml (130 B)
Original SWORD entry document
Author(s)
Kozareva, Velina
•
Martin, Caroline
•
Osorno, Tomas
•
Rudolph, Stephanie
•
Guo, Chong
•
Vanderburg, Charles
•
Nadaf, Naeem
•
Regev, Aviv
•
Regehr, Wade G
•
Macosko, Evan
Date Issued
2021
Journal
Nature
Publisher
Springer Science and Business Media LLC
Citation
Kozareva, Velina, Martin, Caroline, Osorno, Tomas, Rudolph, Stephanie, Guo, Chong et al. 2021. "A transcriptomic atlas of mouse cerebellar cortex comprehensively defines cell types." Nature, 598 (7879).
Version
Final published version
Abstract
AbstractThe cerebellar cortex is a well-studied brain structure with diverse roles in motor learning, coordination, cognition and autonomic regulation. However,  a complete inventory of cerebellar cell types is currently lacking. Here, using recent advances in high-throughput transcriptional profiling1–3, we molecularly define cell types across individual lobules of the adult mouse cerebellum. Purkinje neurons showed considerable regional specialization, with the greatest diversity occurring in the posterior lobules. For several types of cerebellar interneuron, the molecular variation within each type was more continuous, rather than discrete. In particular, for the unipolar brush cells—an interneuron population previously subdivided into discrete populations—the continuous variation in gene expression was associated with a graded continuum of electrophysiological properties. Notably, we found that molecular layer interneurons were composed of two molecularly and functionally distinct types. Both types show a continuum of morphological variation through the thickness of the molecular layer, but electrophysiological recordings revealed marked differences between the two types in spontaneous firing, excitability and electrical coupling. Together, these findings provide a comprehensive cellular atlas of the cerebellar cortex, and outline a methodological and conceptual framework for the integration of molecular, morphological and physiological ontologies for defining brain cell types.
MIT Department
Massachusetts Institute of Technology. Department of Biology
Terms of Use
Creative Commons Attribution 4.0 International license
https://creativecommons.org/licenses/by/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/147092
DOI of Published Version
https://doi.org/10.1038/S41586-021-03220-Z
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.