Orr Miranda E, Garbarino Valentina R, Salinas Angelica, Buffenstein Rochelle
Department of Physiology, University of Texas Health Science Center at San AntonioSan Antonio, TX, USA; The Barshop Institute for Longevity, Aging Studies, University of Texas Health Science Center at San AntonioSan Antonio, TX, USA.
Department of Physiology, University of Texas Health Science Center at San Antonio San Antonio, TX, USA.
Front Neurosci. 2016 Nov 8;10:504. doi: 10.3389/fnins.2016.00504. eCollection 2016.
The naked mole-rat (NMR) is the longest-lived rodent with a maximum lifespan >31 years. Intriguingly, fully-grown naked mole-rats (NMRs) exhibit many traits typical of neonatal rodents. However, little is known about NMR growth and maturation, and we question whether sustained neotenous features when compared to mice, reflect an extended developmental period, commensurate with their exceptionally long life. We tracked development from birth to 3 years of age in the slowest maturing organ, the brain, by measuring mass, neural stem cell proliferation, axonal, and dendritic maturation, synaptogenesis and myelination. NMR brain maturation was compared to data from similar sized rodents, mice, and to that of long-lived mammals, humans, and non-human primates. We found that at birth, NMR brains are significantly more developed than mice, and rather are more similar to those of newborn primates, with clearly laminated hippocampi and myelinated white matter tracts. Despite this more mature brain at birth than mice, postnatal NMR brain maturation occurs at a far slower rate than mice, taking four-times longer than required for mice to fully complete brain development. At 4 months of age, NMR brains reach 90% of adult size with stable neuronal cytostructural protein expression whereas myelin protein expression does not plateau until 9 months of age in NMRs, and synaptic protein expression continues to change throughout the first 3 years of life. Intriguingly, NMR axonal composition is more similar to humans than mice whereby NMRs maintain expression of three-repeat (3R) tau even after brain growth is complete; mice experience an abrupt downregulation of 3R tau by postnatal day 8 which continues to diminish through 6 weeks of age. We have identified key ages in NMR cerebral development and suggest that the long-lived NMR may provide neurobiologists an exceptional model to study brain developmental processes that are compressed in common short-lived laboratory animal models.
裸鼹鼠是寿命最长的啮齿动物,最大寿命超过31年。有趣的是,成年裸鼹鼠表现出许多新生啮齿动物的典型特征。然而,人们对裸鼹鼠的生长和成熟了解甚少,我们质疑与小鼠相比,持续的幼态特征是否反映了一个延长的发育期,与其超长的寿命相称。我们通过测量质量、神经干细胞增殖、轴突和树突成熟、突触形成和髓鞘形成,追踪了生长最慢的器官——大脑从出生到3岁的发育过程。将裸鼹鼠大脑的成熟情况与类似大小的啮齿动物(小鼠)以及长寿哺乳动物(人类和非人类灵长类动物)的数据进行了比较。我们发现,出生时,裸鼹鼠的大脑比小鼠发育得更成熟,更类似于新生灵长类动物的大脑,海马体有明显的分层,白质束有髓鞘。尽管出生时裸鼹鼠的大脑比小鼠更成熟,但出生后裸鼹鼠大脑的成熟速度比小鼠慢得多,完成大脑完全发育所需的时间是小鼠的四倍。在4个月大时,裸鼹鼠的大脑达到成年大小的90%,神经元细胞结构蛋白表达稳定,而髓磷脂蛋白表达直到裸鼹鼠9个月大时才趋于平稳,突触蛋白表达在生命的前3年持续变化。有趣的是,裸鼹鼠的轴突组成与人类比与小鼠更相似,即使在大脑生长完成后,裸鼹鼠仍维持三重复(3R)tau蛋白的表达;小鼠在出生后第8天3R tau蛋白会突然下调,并在6周龄前持续减少。我们确定了裸鼹鼠大脑发育的关键时期,并表明长寿的裸鼹鼠可能为神经生物学家提供一个特殊的模型,用于研究在常见的短寿命实验动物模型中被压缩的大脑发育过程。