Voronkov D N, Stavrovskaya A V, Olshanskiy A S, Lebedeva O S, Illarioshkin S N
Research Center of Neurology, Moscow, Russia.
Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical-Biological Agency of Russia, Moscow, Russia.
Bull Exp Biol Med. 2025 Aug 29. doi: 10.1007/s10517-025-06469-w.
In the experiment with transplantation of neuronal mesencephalic precursors derived from induced pluripotent stem cells into the striatum of rats with unilateral 6-OHDA destruction of the substantia nigra, we evaluated changes in the immunostaining for α-synuclein during differentiation and maturation of grafted neurons 1, 3, and 6 months after the surgery. The content of α-synuclein in transplanted neurons peaked by the third month after surgery, as well as changes in the nuclear-cytoplasmic ratio of α-synuclein in neurons by the 3rd and 6th months relative to the 1st month after transplantation were revealed. Changes in α-synuclein localization and content were associated with a gradual decrease in doublecortin expression and an increase in immunostaining for neuronal enolase and synaptophysin as the graft matured. The high content of total α-synuclein in developing neurons may be a key factor of spreading of α-synuclein toxic species in graft cells and a cause of cell damage.
在将源自诱导多能干细胞的中脑神经元前体细胞移植到单侧6-羟基多巴胺损毁黑质的大鼠纹状体的实验中,我们评估了术后1个月、3个月和6个月移植神经元分化和成熟过程中α-突触核蛋白免疫染色的变化。移植神经元中α-突触核蛋白的含量在术后第三个月达到峰值,并且相对于移植后第1个月,在第3个月和第6个月时神经元中α-突触核蛋白的核质比也出现了变化。随着移植物成熟,α-突触核蛋白定位和含量的变化与双皮质素表达逐渐降低以及神经元烯醇化酶和突触素免疫染色增加有关。发育中神经元中总α-突触核蛋白的高含量可能是α-突触核蛋白毒性物质在移植细胞中扩散的关键因素以及细胞损伤的原因。