Single-Cell RNA-Seq Reveals Hypothalamic Cell Diversity

被引:317
作者
Chen, Renchao [1 ,2 ,3 ]
Wu, Xiaoji [1 ,2 ,3 ]
Jiang, Lan [1 ,2 ,3 ]
Zhang, Yi [1 ,2 ,3 ,4 ,5 ]
机构
[1] Boston Childrens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
[3] Boston Childrens Hosp, Dept Pediat, Div Hematol Oncol, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Genet, Boston, MA 02115 USA
[5] Harvard Stem Cell Inst, WAB 149G,200 Longwood Ave, Boston, MA 02115 USA
关键词
CENTRAL-NERVOUS-SYSTEM; SUPRACHIASMATIC NUCLEUS; ENERGY-BALANCE; FOOD-INTAKE; NEURONS; TRANSCRIPTOMICS; DIFFERENTIATION; TANYCYTES; 3RD-VENTRICLE; SPECIFICATION;
D O I
10.1016/j.celrep.2017.03.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The hypothalamus is one of the most complex brain structures involved in homeostatic regulation. Defining cell composition and identifying cell-type-specific transcriptional features of the hypothalamus is essential for understanding its functions and related disorders. Here, we report single-cell RNA sequencing results of adult mouse hypothalamus, which defines 11 non-neuronal and 34 neuronal cell clusters with distinct transcriptional signatures. Analyses of cell-type-specific transcriptomes reveal gene expression dynamics underlying oligodendrocyte differentiation and tanycyte subtypes. Additionally, data analysis provides a comprehensive view of neuropeptide expression across hypothalamic neuronal subtypes and uncover Crabp1(+) and Pax6(+) neuronal populations in specific hypothalamic subregions. Furthermore, we found food deprivation exhibited differential transcriptional effects among the different neuronal subtypes, suggesting functional specification of various neuronal subtypes. Thus, the work provides a comprehensive transcriptional perspective of adult hypothalamus, which serves as a valuable resource for dissecting cell-type-specific functions of this complex brain region.
引用
收藏
页码:3227 / 3241
页数:15
相关论文
共 46 条
[1]   Hypothalamic tanycytes: potential roles in the control of feeding and energy balance [J].
Bolborea, Matei ;
Dale, Nicholas .
TRENDS IN NEUROSCIENCES, 2013, 36 (02) :91-100
[2]   Isolation and culture of adult neurons and neurospheres [J].
Brewer, Gregory J. ;
Torricelli, John R. .
NATURE PROTOCOLS, 2007, 2 (06) :1490-1498
[3]   Physiological Regulation of Magnocellular Neurosecretory Cell Activity: Integration of Intrinsic, Local and Afferent Mechanisms [J].
Brown, C. H. ;
Bains, J. S. ;
Ludwig, M. ;
Stern, J. E. .
JOURNAL OF NEUROENDOCRINOLOGY, 2013, 25 (08) :678-710
[4]   The oligodendrocyte-specific G protein-coupled receptor GPR17 is a cell-intrinsic timer of myelination [J].
Chen, Ying ;
Wu, Heng ;
Wang, Shuzong ;
Koito, Hisami ;
Li, Jianrong ;
Ye, Feng ;
Hoang, Jenny ;
Escobar, Sabine S. ;
Gow, Alexander ;
Arnett, Heather A. ;
Trapp, Bruce D. ;
Karandikar, Nitin J. ;
Hsieh, Jenny ;
Lu, Q. Richard .
NATURE NEUROSCIENCE, 2009, 12 (11) :1398-1406
[5]   Hypothalamic integration of body fluid regulation [J].
Denton, DA ;
McKinley, MJ ;
Weisinger, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7397-7404
[6]   The Mammalian Circadian Timing System: Organization and Coordination of Central and Peripheral Clocks [J].
Dibner, Charna ;
Schibler, Ueli ;
Albrecht, Urs .
ANNUAL REVIEW OF PHYSIOLOGY, 2010, 72 :517-549
[7]   From lesions to leptin: Hypothalamic control of food intake and body weight [J].
Elmquist, JK ;
Elias, CF ;
Saper, CB .
NEURON, 1999, 22 (02) :221-232
[8]   Transcriptional and Epigenetic Regulation of Oligodendrocyte Development and Myelination in the Central Nervous System [J].
Emery, Ben ;
Lu, Q. Richard .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2015, 7 (09)
[9]   Cellular Taxonomy of the Mouse Striatum as Revealed by Single-Cell RNA-Seq [J].
Gokce, Ozgun ;
Stanley, Geoffrey M. ;
Treutlein, Barbara ;
Neff, Norma F. ;
Camp, J. Gray ;
Malenka, Robert C. ;
Rothwell, Patrick E. ;
Fuccillo, Marc V. ;
Sudhof, Thomas C. ;
Quake, Stephen R. .
CELL REPORTS, 2016, 16 (04) :1126-1137
[10]   A gene expression atlas of the central nervous system based on bacterial artificial chromosomes [J].
Gong, SC ;
Zheng, C ;
Doughty, ML ;
Losos, K ;
Didkovsky, N ;
Schambra, UB ;
Nowak, NJ ;
Joyner, A ;
Leblanc, G ;
Hatten, ME ;
Heintz, N .
NATURE, 2003, 425 (6961) :917-925