Adak Anindyasundar, Das Gaurav, Khan Juhee, Mukherjee Nabanita, Gupta Varsha, Mallesh Rathnam, Ghosh Surajit
Organic and Medicinal Chemistry and Structural Biology and Bioinformatics Divisions, CSIR-Indian Institute of Chemical Biology, 4, Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, West Bengal, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad 201002, India.
ACS Biomater Sci Eng. 2020 Apr 13;6(4):2287-2296. doi: 10.1021/acsbiomaterials.9b01829. Epub 2020 Mar 30.
Brain injury can lead to the loss of neuronal functions and connections, along with the damage of the extracellular matrix (ECM). Thus, it ultimately results in devastating long-term damage, and recovery from this damage is a challenging task. To address this issue, we have designed a sulfo-group-functionalized injectable biocompatible peptide hydrogel, which not only mimics the ECM and supports the damaged neurons but also releases a neurotrophic factor around the injured sites of the brain in the presence of the matrix metalloproteinase 9 (MMP9) enzyme. It has also been observed that the driving force of hydrogel formation is a β-sheet secondary structure and π-π stacking interactions between Phe-Phe moieties. The hydrogel is able not only to promote neurite outgrowth of PC12-derived neurons and primary neurons cultured in its presence but also to nullify the toxic effects of anti-nerve growth factor (Anti-NGF)-induced neurons. It also promotes the expression of vital neuronal markers in rat cortical primary neurons, displays substantial potential in neuroregeneration, and also promotes fast recovery of the sham injured mice brain. Increased expression of reactive astrocytes in the hippocampal dentate gyrus region of the sham injured brain clearly suggests its tremendous ability in the neural repair of the damaged brain. Thus, we can convincingly state that our hydrogel is capable of repairing brain injury by mimicking an ECM-like environment and providing neuroprotection to the damaged neurons.
脑损伤会导致神经元功能和连接的丧失,同时细胞外基质(ECM)也会受损。因此,它最终会造成严重的长期损伤,而从这种损伤中恢复是一项具有挑战性的任务。为了解决这个问题,我们设计了一种磺基功能化的可注射生物相容性肽水凝胶,它不仅能模拟细胞外基质并支持受损神经元,还能在基质金属蛋白酶9(MMP9)存在的情况下,在脑损伤部位周围释放神经营养因子。还观察到水凝胶形成的驱动力是β-折叠二级结构以及苯丙氨酸-苯丙氨酸基团之间的π-π堆积相互作用。这种水凝胶不仅能够促进在其存在下培养的PC12衍生神经元和原代神经元的神经突生长,还能消除抗神经生长因子(Anti-NGF)诱导的神经元的毒性作用。它还能促进大鼠皮质原代神经元中重要神经元标志物的表达,在神经再生方面具有巨大潜力,并且还能促进假损伤小鼠大脑的快速恢复。假损伤大脑海马齿状回区域中反应性星形胶质细胞表达的增加清楚地表明其在受损大脑神经修复方面具有巨大能力。因此,我们可以有说服力地说,我们的水凝胶能够通过模拟类似细胞外基质的环境并为受损神经元提供神经保护来修复脑损伤。