Functional and Developmental Identification of a Molecular Subtype of Brain Serotonergic Neuron Specialized to Regulate Breathing Dynamics

被引:94
作者
Brust, Rachael D. [1 ]
Corcoran, Andrea E. [2 ]
Richerson, George B. [3 ,4 ,5 ]
Nattie, Eugene [2 ]
Dymecki, Susan M. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Geisel Sch Med Dartmouth, Dept Physiol & Neurobiol, Lebanon, NH 03756 USA
[3] Univ Iowa, Dept Neurol, Iowa City, IA 52242 USA
[4] Univ Iowa, Dept Mol Physiol & Biophys, Iowa City, IA 52242 USA
[5] Vet Affairs Med Ctr, Iowa City, IA 52246 USA
关键词
INFANT-DEATH-SYNDROME; LOCUS-COERULEUS; CENTRAL CHEMOSENSITIVITY; RESPIRATORY CONTROL; RAPHE NEURONS; SUBSTANCE-P; RAT; CO2; NUCLEUS; SYSTEM;
D O I
10.1016/j.celrep.2014.11.027
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Serotonergic neurons modulate behavioral and physiological responses from aggression and anxiety to breathing and thermoregulation. Disorders involving serotonin (5HT) dysregulation are commensurately heterogeneous and numerous. We hypothesized that this breadth in functionality derives in part from a developmentally determined substructure of distinct subtypes of 5HT neurons each specialized to modulate specific behaviors. By manipulating developmentally defined subgroups one by one chemogenetically, we find that the Egr2-Pet1 subgroup is specialized to drive increased ventilation in response to carbon dioxide elevation and acidosis. Furthermore, this subtype exhibits intrinsic chemosensitivity and modality-specific projections-increasing firing during hypercapnic acidosis and selectively projecting to respiratory chemosensory but not motor centers, respectively. These findings show that serotonergic regulation of the respiratory chemoreflex is mediated by a specialized molecular subtype of 5HT neuron harboring unique physiological, biophysical, and hodological properties specified developmentally and demonstrate that the serotonergic system contains specialized modules contributing to its collective functional breadth.
引用
收藏
页码:2152 / 2165
页数:14
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