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A marmoset brain cell census reveals regional specialization of cellular identities

The mammalian brain is composed of many brain structures, each with its own ontogenetic and developmental history. We used single-nucleus RNA sequencing to sample over 2.4 million brain cells across 18 locations in the common marmoset, a New World monkey primed for genetic engineering, and examined...

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Autores principales: Krienen, Fenna M., Levandowski, Kirsten M., Zaniewski, Heather, del Rosario, Ricardo C.H., Schroeder, Margaret E., Goldman, Melissa, Wienisch, Martin, Lutservitz, Alyssa, Beja-Glasser, Victoria F., Chen, Cindy, Zhang, Qiangge, Chan, Ken Y., Li, Katelyn X., Sharma, Jitendra, McCormack, Dana, Shin, Tay Won, Harrahill, Andrew, Nyase, Eric, Mudhar, Gagandeep, Mauermann, Abigail, Wysoker, Alec, Nemesh, James, Kashin, Seva, Vergara, Josselyn, Chelini, Gabriele, Dimidschstein, Jordane, Berretta, Sabina, Deverman, Benjamin E., Boyden, Ed, McCarroll, Steven A., Feng, Guoping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569717/
https://www.ncbi.nlm.nih.gov/pubmed/37824615
http://dx.doi.org/10.1126/sciadv.adk3986
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author Krienen, Fenna M.
Levandowski, Kirsten M.
Zaniewski, Heather
del Rosario, Ricardo C.H.
Schroeder, Margaret E.
Goldman, Melissa
Wienisch, Martin
Lutservitz, Alyssa
Beja-Glasser, Victoria F.
Chen, Cindy
Zhang, Qiangge
Chan, Ken Y.
Li, Katelyn X.
Sharma, Jitendra
McCormack, Dana
Shin, Tay Won
Harrahill, Andrew
Nyase, Eric
Mudhar, Gagandeep
Mauermann, Abigail
Wysoker, Alec
Nemesh, James
Kashin, Seva
Vergara, Josselyn
Chelini, Gabriele
Dimidschstein, Jordane
Berretta, Sabina
Deverman, Benjamin E.
Boyden, Ed
McCarroll, Steven A.
Feng, Guoping
author_facet Krienen, Fenna M.
Levandowski, Kirsten M.
Zaniewski, Heather
del Rosario, Ricardo C.H.
Schroeder, Margaret E.
Goldman, Melissa
Wienisch, Martin
Lutservitz, Alyssa
Beja-Glasser, Victoria F.
Chen, Cindy
Zhang, Qiangge
Chan, Ken Y.
Li, Katelyn X.
Sharma, Jitendra
McCormack, Dana
Shin, Tay Won
Harrahill, Andrew
Nyase, Eric
Mudhar, Gagandeep
Mauermann, Abigail
Wysoker, Alec
Nemesh, James
Kashin, Seva
Vergara, Josselyn
Chelini, Gabriele
Dimidschstein, Jordane
Berretta, Sabina
Deverman, Benjamin E.
Boyden, Ed
McCarroll, Steven A.
Feng, Guoping
author_sort Krienen, Fenna M.
collection PubMed
description The mammalian brain is composed of many brain structures, each with its own ontogenetic and developmental history. We used single-nucleus RNA sequencing to sample over 2.4 million brain cells across 18 locations in the common marmoset, a New World monkey primed for genetic engineering, and examined gene expression patterns of cell types within and across brain structures. The adult transcriptomic identity of most neuronal types is shaped more by developmental origin than by neurotransmitter signaling repertoire. Quantitative mapping of GABAergic types with single-molecule FISH (smFISH) reveals that interneurons in the striatum and neocortex follow distinct spatial principles, and that lateral prefrontal and other higher-order cortical association areas are distinguished by high proportions of VIP(+) neurons. We use cell type–specific enhancers to drive AAV-GFP and reconstruct the morphologies of molecularly resolved interneuron types in neocortex and striatum. Our analyses highlight how lineage, local context, and functional class contribute to the transcriptional identity and biodistribution of primate brain cell types.
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spelling pubmed-105697172023-10-13 A marmoset brain cell census reveals regional specialization of cellular identities Krienen, Fenna M. Levandowski, Kirsten M. Zaniewski, Heather del Rosario, Ricardo C.H. Schroeder, Margaret E. Goldman, Melissa Wienisch, Martin Lutservitz, Alyssa Beja-Glasser, Victoria F. Chen, Cindy Zhang, Qiangge Chan, Ken Y. Li, Katelyn X. Sharma, Jitendra McCormack, Dana Shin, Tay Won Harrahill, Andrew Nyase, Eric Mudhar, Gagandeep Mauermann, Abigail Wysoker, Alec Nemesh, James Kashin, Seva Vergara, Josselyn Chelini, Gabriele Dimidschstein, Jordane Berretta, Sabina Deverman, Benjamin E. Boyden, Ed McCarroll, Steven A. Feng, Guoping Sci Adv Neuroscience The mammalian brain is composed of many brain structures, each with its own ontogenetic and developmental history. We used single-nucleus RNA sequencing to sample over 2.4 million brain cells across 18 locations in the common marmoset, a New World monkey primed for genetic engineering, and examined gene expression patterns of cell types within and across brain structures. The adult transcriptomic identity of most neuronal types is shaped more by developmental origin than by neurotransmitter signaling repertoire. Quantitative mapping of GABAergic types with single-molecule FISH (smFISH) reveals that interneurons in the striatum and neocortex follow distinct spatial principles, and that lateral prefrontal and other higher-order cortical association areas are distinguished by high proportions of VIP(+) neurons. We use cell type–specific enhancers to drive AAV-GFP and reconstruct the morphologies of molecularly resolved interneuron types in neocortex and striatum. Our analyses highlight how lineage, local context, and functional class contribute to the transcriptional identity and biodistribution of primate brain cell types. American Association for the Advancement of Science 2023-10-12 /pmc/articles/PMC10569717/ /pubmed/37824615 http://dx.doi.org/10.1126/sciadv.adk3986 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Neuroscience
Krienen, Fenna M.
Levandowski, Kirsten M.
Zaniewski, Heather
del Rosario, Ricardo C.H.
Schroeder, Margaret E.
Goldman, Melissa
Wienisch, Martin
Lutservitz, Alyssa
Beja-Glasser, Victoria F.
Chen, Cindy
Zhang, Qiangge
Chan, Ken Y.
Li, Katelyn X.
Sharma, Jitendra
McCormack, Dana
Shin, Tay Won
Harrahill, Andrew
Nyase, Eric
Mudhar, Gagandeep
Mauermann, Abigail
Wysoker, Alec
Nemesh, James
Kashin, Seva
Vergara, Josselyn
Chelini, Gabriele
Dimidschstein, Jordane
Berretta, Sabina
Deverman, Benjamin E.
Boyden, Ed
McCarroll, Steven A.
Feng, Guoping
A marmoset brain cell census reveals regional specialization of cellular identities
title A marmoset brain cell census reveals regional specialization of cellular identities
title_full A marmoset brain cell census reveals regional specialization of cellular identities
title_fullStr A marmoset brain cell census reveals regional specialization of cellular identities
title_full_unstemmed A marmoset brain cell census reveals regional specialization of cellular identities
title_short A marmoset brain cell census reveals regional specialization of cellular identities
title_sort marmoset brain cell census reveals regional specialization of cellular identities
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569717/
https://www.ncbi.nlm.nih.gov/pubmed/37824615
http://dx.doi.org/10.1126/sciadv.adk3986
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