S-Inova Biotech, Programa de Pós-graduação em Biotecnologia, Universidade Católica Dom Bosco, Campo Grande 79117-900, Mato Grosso do Sul, Brazil.
Laboratório de Purificação de Proteínas e suas Funções Biológicas, Unidade de Tecnologia de Alimentos e da Saúde Pública, Universidade Federal de Mato Grosso do Sul, Campo Grande 79070-900, Mato Grosso do Sul, Brazil.
Toxins (Basel). 2022 Oct 11;14(10):696. doi: 10.3390/toxins14100696.
The importance of neuroinflammation in neurology is becoming increasingly apparent. In addition to neuroinflammatory diseases such as multiple sclerosis, the role of neuroinflammation has been identified in many non-inflammatory neurological disorders such as stroke, epilepsy, and cancer. The immune response within the brain involves the presence of CNS resident cells; mainly glial cells, such as microglia, the CNS resident macrophages. We evaluated the peptide Ca-MAP1 bioinspired on the immature cytolytic toxin candidalysin to develop a less hemolytic peptide with anti-neuroinflammatory, antibacterial, and cytotoxic activity against tumor cells. and studies were performed at various concentrations. Ca-MAP1 exhibits low hemolytic activity at lower concentrations and was not cytotoxic to MRC-5 and BV-2 cells. Ca-MAP1 showed activity against , ATCC, KPC, ATCC, , and ATCC. Furthermore, Ca-MAP1 exhibits anti-neuroinflammatory activity in the BV-2 microglia model, with 93.78% inhibition of nitrate production at 18.1 µM. Ca-MAP1 presents cytotoxic activity against tumor cell line NCI-H292 at 36.3 μM, with an IC of 38.4 µM. Ca-MAP1 demonstrates results that qualify it to be evaluated in the next steps to promote the control of infections and provide an alternative antitumor therapy.
神经炎症在神经病学中的重要性日益明显。除了多发性硬化等神经炎症性疾病外,神经炎症的作用在许多非炎症性神经疾病中也得到了证实,如中风、癫痫和癌症。大脑中的免疫反应涉及中枢神经系统固有细胞的存在;主要是神经胶质细胞,如小胶质细胞,中枢神经系统固有巨噬细胞。我们评估了基于不成熟细胞溶解毒素念珠菌素的肽 Ca-MAP1,以开发一种具有抗神经炎症、抗菌和细胞毒性活性的肽,针对肿瘤细胞。并在不同浓度下进行了研究。Ca-MAP1 在较低浓度下表现出较低的溶血活性,对 MRC-5 和 BV-2 细胞没有细胞毒性。Ca-MAP1 对 、ATCC、KPC、ATCC、、和 ATCC 均有活性。此外,Ca-MAP1 在 BV-2 小胶质细胞模型中表现出抗神经炎症活性,在 18.1 µM 时抑制硝酸盐生成 93.78%。Ca-MAP1 对肿瘤细胞系 NCI-H292 的细胞毒性活性在 36.3 μM 时为 38.4 μM。Ca-MAP1 表现出的结果使其有资格在下一步进行评估,以促进感染控制并提供抗肿瘤治疗的替代方案。