Physiological roles for the subfornical organ: a dynamic transcriptome shaped by autonomic state

被引:27
作者
Hindmarch, Charles Colin Thomas [1 ,2 ]
Ferguson, Alastair V. [3 ]
机构
[1] Univ Bristol, Sch Clin Sci, Dorothy Hodgkin Bldg, Bristol BS1 3NY, Avon, England
[2] Univ Malaya, Fac Med, Dept Physiol, Kuala Lumpur 50603, Malaysia
[3] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K7L 3N6, Canada
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2016年 / 594卷 / 06期
基金
英国生物技术与生命科学研究理事会;
关键词
SENSORY CIRCUMVENTRICULAR ORGANS; AREA POSTREMA NEURONS; MESSENGER RIBONUCLEIC-ACIDS; CENTRAL-NERVOUS-SYSTEM; BLOOD-BRAIN-BARRIER; LONG-TERM CONTROL; PARAVENTRICULAR NUCLEUS; MAGNOCELLULAR NEURONS; RESPONSIVE NEURONS; SUPRAOPTIC NUCLEUS;
D O I
10.1113/JP270726
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The subfornical organ (SFO) is a circumventricular organ recognized for its ability to sense and integrate hydromineral and hormonal circulating fluid balance signals, information which is transmitted to central autonomic nuclei to which SFO neurons project. While the role of SFO was once synonymous with physiological responses to osmotic, volumetric and cardiovascular challenge, recent data suggest that SFO neurons also sense and integrate information from circulating signals of metabolic status. Using microarrays, we have confirmed the expression of receptors already described in the SFO, and identified many novel transcripts expressed in this circumventricular organ including receptors for many of the critical circulating energy balance signals such as adiponectin, apelin, endocannabinoids, leptin, insulin and peptide YY. This transcriptome analysis also identified SFO transcripts, the expressions of which are significantly changed by either 72h dehydration, or 48h starvation, compared to fed and euhydrated controls. Expression and potential roles for many of these targets are yet to be confirmed and elucidated. Subsequent validation of data for adiponectin and leptin receptors confirmed that receptors for both are expressed in the SFO, that discrete populations of neurons in this tissue are functionally responsive to these adipokines, and that such responsiveness is regulated by physiological state. Thus, transcriptomic analysis offers great promise for understanding the integrative complexity of these physiological systems, especially with development of technologies allowing description of the entire transcriptome of single, carefully phenotyped, SFO neurons. These data will ultimately elucidate mechanisms through which these uniquely positioned neurons respond to and integrate complex circulating signals.
引用
收藏
页码:1581 / 1589
页数:9
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