Area postrema undergoes dynamic postnatal changes in mice and humans.
Area postrema undergoes dynamic postnatal changes in mice and humans.
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区域postrema经历小鼠和人类的产后变化。
DOI:
10.1002/cne.23903
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发表时间:
2016-04-15
期刊:
影响因子:
--
通讯作者:
Otero JJ
中科院分区:
文献类型:
--
作者:
Gokozan HN;Baig F;Corcoran S;Catacutan FP;Gygli PE;Takakura AC;Moreira TS;Czeisler C;Otero JJ
The post-natal period in mammals represents a developmental epoch of significant change in the autonomic nervous system (ANS). In this study we focus on post-natal development of the area postrema, a crucial ANS structure that regulates temperature, breathing, and satiety, amongst other activities. We find that the human area postrema undergoes significant developmental changes during post-natal development. To further characterize these changes, we utilized transgenic mouse reagents to delineate neuronal circuitry. We discovered that although a well-formed ANS scaffold exists early in embryonic development, the area postrema shows a delayed maturation. Specifically, postnatal days 0 to 7 in mice show no significant change in area postrema volume or synaptic input from PHOX2B-derived neurons. In contrast, postnatal days 7-20 shows a significant increase in volume and synaptic input from PHOX2B-derived neurons. We conclude that key ANS structures show an unexpected dynamic developmental changes during post-natal development. These data provide a basis for understanding ANS dysfunction and disease predisposition in premature and post-natal humans. The area postrema is a major integrator of the autonomic nervous system (ANS). At birth, mammals show ANS immaturity resulting in generalized dysautonomia. Here, Gokozan et al. by combining modern and traditional neuroanatomical tools demonstrate that the development of the area postrema dynamically changes during postnatal development in mice and humans. These changes include a significant increase in size and increase in the innervation during the post-natal epoch. The graphical abstract above illustrates the increase in area postrema size and in synaptic vessicles derived from PHOX2B-derived neurons that we identified in this work.