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Photodynamic damage of glial cells in crayfish ventral nerve cord

机译:小龙虾腹神经索中神经胶质细胞的光动力损伤

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Photodynamic therapy (PDT) is a promising method for treatment of brain tumors, the most of which are of glial origin. In the present work we studied PDT-mediated injury of glial cells in nerve tissue, specifically, in abdominal connectives in the crayfish ventral nerve cord. The preparation was photosensitized with alumophthalocyanine Photosens and irradiated 30 min with the diode laser (670 nm, 0.1 or 0.15 W/cm2). After following incubation in the darkness during 1- 10 hours it was fluorochromed with Hoechst 33342 and propidium iodide to reveal nuclei of living, necrotic and apoptotic cells. The chain-like location of the glial nuclei allowed visualization of those enveloping giant axons and blood vessels. The level of glial necrosis in control preparations was about 2-5 %. Apoptosis was not observed in control preparations. PDT significantly increased necrosis of glial cells to 52 or 67 % just after irradiation with 0.1 or 0.15 W/cm2, respectively. Apoptosis of glial cells was observed only at 10 hours after light exposure. Upper layers of the glial envelope of the connectives were injured stronger comparing to deep ones: the level of glial necrosis decreased from 100 to 30 % upon moving from the connective surface to the plane of the giant axon inside the connective. Survival of glial cells was also high in the vicinity of blood vessels. One can suggest that giant axons and blood vessels protect neighboring glial cells from photodynamic damage. The mechanism of such protective action remains to be elucidated.
机译:光动力疗法(PDT)是一种治疗脑部肿瘤的有前途的方法,其中大多数是神经胶质起源的。在当前的工作中,我们研究了PDT介导的神经组织,特别是小龙虾腹侧神经索腹腔结缔组织中神经胶质细胞的损伤。该制剂用铝酞菁光敏剂光敏,并用二极管激光器(670nm,0.1或0.15W / cm 2)照射30分钟。在黑暗中孵育1-10小时后,将其与Hoechst 33342和碘化丙啶一起进行荧光染色,以显示活细胞,坏死细胞和凋亡细胞的细胞核。胶质细胞核的链状位置可以看到那些包裹着的巨大轴突和血管。对照制剂中神经胶质坏死的水平约为2-5%。在对照制剂中未观察到凋亡。仅在用0.1或0.15 W / cm2照射后,PDT即可将神经胶质细胞的坏死显着增加至52%或67%。仅在光照后10小时观察到神经胶质细胞的凋亡。与深层结缔组织相比,结缔组织胶质囊的上层受到的伤害更大:当从结缔组织表面移至结缔组织内部的巨大轴突平面时,神经胶质坏死的水平从100%下降至30%。在血管附近,神经胶质细胞的存活率也很高。有人认为巨轴突和血管可以保护邻近的神经胶质细胞免受光动力损害。这种保护作用的机理尚待阐明。

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