4.8 Article

High-Throughput Mapping of Long-Range Neuronal Projection Using In Situ Sequencing

期刊

CELL
卷 179, 期 3, 页码 772-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2019.09.023

关键词

-

资金

  1. NIH [5P30CA045508, 5RO1NS073129, 5RO1DA036913]
  2. Brain Research Foundation [BRF-SIA-2014-03]
  3. Simons Foundation [382793/SIMONS]
  4. Paul Allen Distinguished Investigator Award
  5. Simons Foundation
  6. IARPA MICrONS [D16PC0008]

向作者/读者索取更多资源

Understanding neural circuits requires deciphering interactions among myriad cell types defined by spatial organization, connectivity, gene expression, and other properties. Resolving these cell types requires both single-neuron resolution and high throughput, a challenging combination with conventional methods. Here, we introduce barcoded anatomy resolved by sequencing (BARseq), a multiplexed method based on RNA barcoding for mapping projections of thousands of spatially resolved neurons in a single brain and relating those projections to other properties such as gene or Cre expression. Mapping the projections to 11 areas of 3,579 neurons in mouse auditory cortex using BARseq confirmed the laminar organization of the three top classes (intratelencephalic [IT], pyramidal tract-like [PT-like], and corticothalamic [CT]) of projection neurons. In depth analysis uncovered a projection type restricted almost exclusively to transcriptionally defined subtypes of IT neurons. By bridging anatomical and transcriptomic approaches at cellular resolution with high throughput, BARseq can potentially uncover the organizing principles underlying the structure and formation of neural circuits.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据