Mermet-Joret Noemie, Chatila Nadwa, Pereira Bruno, Monconduit Lénaic, Dallel Radhouane, Antri Myriam
Neuro-Dol, Clermont Université, Université D'Auvergne, BP 10448, F-63000, Clermont-Ferrand & Inserm U1107, Clermont-Ferrand, F-63100, France.
Biostatistics Unit (DRCI), CHU Clermont-Ferrand, Clermont-Ferrand, F-63100, France.
Dev Neurobiol. 2017 Jan;77(1):102-119. doi: 10.1002/dneu.22414. Epub 2016 Jun 30.
Protein kinase C gamma (PKCγ) interneurons, located in the superficial spinal (SDH) and medullary dorsal horns (MDH), have been shown to play a critical role in cutaneous mechanical hypersensitivity. However, a thorough characterization of their development in the MDH is lacking. Here, it is shown that the number of PKCγ-ir interneurons changes from postnatal day 3 (P3) to P60 (adult) and such developmental changes differ according to laminae. PKCγ-ir interneurons are already present at P3-5 in laminae I, IIo, and III. In lamina III, they then decrease from P11-P15 to P60. Interestingly, PKCγ-ir interneurons appear only at P6 in lamina IIi, and they conversely increase to reach adult levels at P11-15. Analysis of neurogenesis using bromodeoxyuridine (BrdU) does not detect any PKCγ-BrdU double-labeling in lamina IIi. Quantification of the neuronal marker, NeuN, reveals a sharp neuronal decline (∼50%) within all superficial MDH laminae during early development (P3-15), suggesting that developmental changes in PKCγ-ir interneurons are independent from those of other neurons. Finally, neonatal capsaicin treatment, which produces a permanent loss of most unmyelinated afferent fibers, has no effect on the development of PKCγ-ir interneurons. Together, the results show that: (i) the expression of PKCγ-ir interneurons in MDH is developmentally regulated with a critical period at P11-P15, (ii) PKCγ-ir interneurons are developmentally heterogeneous, (iii) lamina IIi PKCγ-ir interneurons appear less vulnerable to cell death, and (iv) postnatal maturation of PKCγ-ir interneurons is due to neither neurogenesis, nor neuronal migration, and is independent of C-fiber development. © 2016 Wiley Periodicals, Inc. Develop Neurobiol 77: 102-119, 2017.
蛋白激酶Cγ(PKCγ)中间神经元位于脊髓浅层背角(SDH)和延髓背角(MDH),已被证明在皮肤机械性超敏反应中起关键作用。然而,目前尚缺乏对其在MDH中发育的全面描述。在此研究中,发现PKCγ免疫反应性中间神经元的数量在出生后第3天(P3)至第60天(成年期)发生变化,并且这种发育变化因板层而异。在I层、IIo层和III层中,PKCγ免疫反应性中间神经元在P3 - 5时就已存在。在III层中,它们随后从P11 - P15减少至P60。有趣的是,PKCγ免疫反应性中间神经元仅在IIi层的P6时出现,相反,它们在P11 - 15时增加至成年水平。使用溴脱氧尿苷(BrdU)进行神经发生分析未在IIi层中检测到任何PKCγ - BrdU双标记。对神经元标记物NeuN的定量分析显示,在早期发育阶段(P3 - 15),所有浅层MDH板层中的神经元数量急剧下降(约50%),这表明PKCγ免疫反应性中间神经元的发育变化与其他神经元的变化无关。最后,新生期辣椒素处理会导致大多数无髓传入纤维永久性丧失,但对PKCγ免疫反应性中间神经元的发育没有影响。总之,结果表明:(i)MDH中PKCγ免疫反应性中间神经元的表达在发育过程中受到调节,关键时期为P11 - P15;(ii)PKCγ免疫反应性中间神经元在发育过程中具有异质性;(iii)IIi层PKCγ免疫反应性中间神经元似乎对细胞死亡不太敏感;(iv)PKCγ免疫反应性中间神经元的出生后成熟既不是由于神经发生,也不是由于神经元迁移,并且与C纤维发育无关。© 2016威利期刊公司。《发育神经生物学》77: 102 - 119, 2017。