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首页> 外文期刊>Stem cells translational medicine. >The Neurofilament-Derived Peptide NFL-TBS.40-63 Targets Neural Stem Cells and Affects Their Properties
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The Neurofilament-Derived Peptide NFL-TBS.40-63 Targets Neural Stem Cells and Affects Their Properties

机译:神经丝衍生肽NFL-TBS.40-63靶向神经干细胞并影响其性能

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Targeting neural stem cells (NSCs) in the adult brain represents a promising approach for developing new regenerative strategies, because these cells can proliferate, self-renew, and differentiate into new neurons, astrocytes, and oligodendrocytes. Previous work showed that the NFL-TBS.40-63 peptide, corresponding to the sequence of a tubulin-binding site on neurofilaments, can target glioblastoma cells, where it disrupts their microtubules and inhibits their proliferation. We show that this peptide targets NSCs in vitro and in vivo when injected into the cerebrospinal fluid. Although neurosphere formation was not altered by the peptide, the NSC self-renewal capacity and proliferation were reduced and were associated with increased adhesion and differentiation. These results indicate that the NFL-TBS.40-63 peptide represents a new molecular tool to target NSCs to develop new strategies for regenerative medicine and the treatment of brain tumors.In the present study, the NFL-TBS.40-63 peptide targeted neural stem cells in vitro when isolated from the subventricular zone and in vivo when injected into the cerebrospinal fluid present in the lateral ventricle. The in vitro formation of neurospheres was not altered by the peptide; however, at a high concentration of the peptide, the neural stem cell (NSC) self-renewal capacity and proliferation were reduced and associated with increased adhesion and differentiation. These results indicate that the NFL-TBS.40-63 peptide represents a new molecular tool to target NSCs to develop new strategies for regenerative medicine and the treatment of brain tumors.
机译:针对成年大脑中的神经干细胞(NSC)是开发新的再生策略的有前途的方法,因为这些细胞可以增殖,自我更新并分化为新的神经元,星形胶质细胞和少突胶质细胞。先前的工作表明,与神经丝上微管蛋白结合位点的序列相对应的NFL-TBS.40-63肽可以靶向胶质母细胞瘤细胞,从而破坏其微管并抑制其增殖。我们表明,当注射入脑脊液中时,该肽可在体外和体内靶向NSC。尽管肽不会改变神经球的形成,但NSC的自我更新能力和增殖却降低了,并且与粘附和分化的增加有关。这些结果表明NFL-TBS.40-63肽代表了靶向NSC的新分子工具,以开发再生医学和脑肿瘤治疗的新策略。在本研究中,NFL-TBS.40-63肽靶向神经干细胞在体外从脑室下区分离时,在体内注射到侧脑室中存在的脑脊髓液中时。肽不会改变体外神经球的形成;然而,在高浓度的肽下,神经干细胞(NSC)的自我更新能力和增殖能力降低,并与粘附和分化增加有关。这些结果表明,NFL-TBS.40-63肽代表一种靶向NSC的新分子工具,以开发再生医学和脑肿瘤治疗的新策略。

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