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Single-Cell Transcriptional Analysis Reveals Novel Neuronal Phenotypes and Interaction Networks Involved in the Central Circadian Clock
by
Zhu, Haisun
, Ogunnaike, Babatunde A.
, Park, James
, O'Sullivan, Sean
, Weaver, David R.
, Vadigepalli, Rajanikanth
, Schwaber, James S.
in
Biological clocks
/ Biomarkers
/ Cell-network
/ Circadian rhythm
/ Circadian rhythms
/ Community structure
/ Functional morphology
/ Gene expression
/ Genomics
/ Light
/ Localization
/ Mammals
/ network topology
/ Neurogenesis
/ Neurons
/ Neuroscience
/ Neurosciences
/ Paracrine signalling
/ Phenotypes
/ Single-cells
/ Suprachiasmatic nucleus
/ Transcription
/ Transcriptional heterogeneity
/ transcriptional phenotypes
2016
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Single-Cell Transcriptional Analysis Reveals Novel Neuronal Phenotypes and Interaction Networks Involved in the Central Circadian Clock
by
Zhu, Haisun
, Ogunnaike, Babatunde A.
, Park, James
, O'Sullivan, Sean
, Weaver, David R.
, Vadigepalli, Rajanikanth
, Schwaber, James S.
in
Biological clocks
/ Biomarkers
/ Cell-network
/ Circadian rhythm
/ Circadian rhythms
/ Community structure
/ Functional morphology
/ Gene expression
/ Genomics
/ Light
/ Localization
/ Mammals
/ network topology
/ Neurogenesis
/ Neurons
/ Neuroscience
/ Neurosciences
/ Paracrine signalling
/ Phenotypes
/ Single-cells
/ Suprachiasmatic nucleus
/ Transcription
/ Transcriptional heterogeneity
/ transcriptional phenotypes
2016
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Single-Cell Transcriptional Analysis Reveals Novel Neuronal Phenotypes and Interaction Networks Involved in the Central Circadian Clock
by
Zhu, Haisun
, Ogunnaike, Babatunde A.
, Park, James
, O'Sullivan, Sean
, Weaver, David R.
, Vadigepalli, Rajanikanth
, Schwaber, James S.
in
Biological clocks
/ Biomarkers
/ Cell-network
/ Circadian rhythm
/ Circadian rhythms
/ Community structure
/ Functional morphology
/ Gene expression
/ Genomics
/ Light
/ Localization
/ Mammals
/ network topology
/ Neurogenesis
/ Neurons
/ Neuroscience
/ Neurosciences
/ Paracrine signalling
/ Phenotypes
/ Single-cells
/ Suprachiasmatic nucleus
/ Transcription
/ Transcriptional heterogeneity
/ transcriptional phenotypes
2016
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Single-Cell Transcriptional Analysis Reveals Novel Neuronal Phenotypes and Interaction Networks Involved in the Central Circadian Clock
Journal Article
Single-Cell Transcriptional Analysis Reveals Novel Neuronal Phenotypes and Interaction Networks Involved in the Central Circadian Clock
2016
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Overview
Single-cell heterogeneity confounds efforts to understand how a population of cells organizes into cellular networks that underlie tissue-level function. This complexity is prominent in the mammalian suprachiasmatic nucleus (SCN). Here, individual neurons exhibit a remarkable amount of asynchronous behavior and transcriptional heterogeneity. However, SCN neurons are able to generate precisely coordinated synaptic and molecular outputs that synchronize the body to a common circadian cycle by organizing into cellular networks. To understand this emergent cellular network property, it is important to reconcile single-neuron heterogeneity with network organization. In light of recent studies suggesting that transcriptionally heterogeneous cells organize into distinct cellular phenotypes, we characterized the transcriptional, spatial, and functional organization of 352 SCN neurons from mice experiencing phase-shifts in their circadian cycle. Using the community structure detection method and multivariate analytical techniques, we identified previously undescribed neuronal phenotypes that are likely to participate in regulatory networks with known SCN cell types. Based on the newly discovered neuronal phenotypes, we developed a data-driven neuronal network structure in which multiple cell types interact through known synaptic and paracrine signaling mechanisms. These results provide a basis from which to interpret the functional variability of SCN neurons and describe methodologies toward understanding how a population of heterogeneous single cells organizes into cellular networks that underlie tissue-level function.
Publisher
Frontiers Research Foundation,Frontiers Media S.A
Subject
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