Research Institute, Nano Intelligent Biomedical Engineering Corporation (NIBEC), Seoul, 03127, Republic of Korea.
Department of Dental Regenerative Biotechnology and Dental Research Institute, School of Dentistry, Seoul National University, #403 Biomaterial Research Building, 101 Daehak-ro, Jongno-gu, Seoul, 03080, Republic of Korea.
Tissue Eng Regen Med. 2023 Oct;20(6):965-979. doi: 10.1007/s13770-023-00572-7. Epub 2023 Aug 17.
Inflammatory bowel disease (IBD) is an incurable disease that negatively influences the quality of life of patients. Current and emerging therapies target proinflammatory cytokines and/or receptors to downregulate proinflammatory responses, but insufficient remission requires other therapeutic agents. Herein, we report that the synthetic anti-inflammatory peptide 15 (SAP15) is capable of cell penetration and anti-inflammatory activity in human macrophages.
SAP15 was labeled with fluorescence and administered to human leukemia monocytic cells (THP-1) cells for cell penetration analysis. Using biolayer interferometry analysis, the binding affinity of SAP15 with histone deacetylase 5 (HDAC5) was measured. SAP15-treated THP-1 cells were analyzed by protein phosphorylation assay, flow cytometry, and enzyme-linked immunosorbent assay (ELISA). In addition, in vivo analysis of the therapeutic effect on IBD was observed in a dextran sulfate sodium (DSS)-induced model. Samples from SAP15-treated mice were analyzed at both the macroscopic and microscopic levels using ELISA, myeloperoxidase (MPO) assays, and histological evaluations.
SAP15 was internalized within the cytosol and nucleus of THP-1 cells and bound to the HDAC5 protein. SAP15-treated macrophages were assessed for protein phosphorylation and showed inhibited phosphorylation of HDAC5 and other immune-related proteins, which led to increased M2-like macrophage markers and decreased M1-like macrophage markers and tumor necrosis factor-α and interleukin-6 cytokine levels. The SAP15 treatment on IBD model showed significant recovery of colon length. Further histological analysis of colon demonstrated the therapeutic effect of SAP15 on mucosal layer. Moreover, proinflammatory cytokine levels and MPO activity from the plasma show that SAP15 is effective in reduced proinflammatory responses.
These findings suggest that SAP15 is a novel peptide with a novel cell-penetrating peptide with anti-inflammatory property that can be used as a therapeutic agent for IBD and other inflammatory diseases.
炎症性肠病(IBD)是一种无法治愈的疾病,会降低患者的生活质量。目前和新兴的治疗方法针对促炎细胞因子和/或受体,以下调促炎反应,但缓解不足需要其他治疗药物。在此,我们报告合成抗炎肽 15(SAP15)能够穿透细胞并在人类巨噬细胞中发挥抗炎活性。
用荧光标记 SAP15,并将其施用于人白血病单核细胞(THP-1)细胞进行细胞穿透分析。使用生物层干涉分析测量 SAP15 与组蛋白去乙酰化酶 5(HDAC5)的结合亲和力。通过蛋白磷酸化测定、流式细胞术和酶联免疫吸附测定(ELISA)分析 SAP15 处理的 THP-1 细胞。此外,在葡聚糖硫酸钠(DSS)诱导模型中观察 SAP15 对 IBD 的治疗作用的体内分析。使用 ELISA、髓过氧化物酶(MPO)测定和组织学评估分析 SAP15 治疗小鼠的样本。
SAP15 被内化到 THP-1 细胞的细胞质和核内,并与 HDAC5 蛋白结合。对 SAP15 处理的巨噬细胞进行蛋白磷酸化评估,发现 SAP15 抑制了 HDAC5 和其他免疫相关蛋白的磷酸化,导致 M2 样巨噬细胞标志物增加,M1 样巨噬细胞标志物和肿瘤坏死因子-α和白细胞介素-6 细胞因子水平降低。SAP15 对 IBD 模型的治疗作用显示出结肠长度的显著恢复。对结肠的进一步组织学分析表明 SAP15 对粘膜层有治疗作用。此外,来自血浆的促炎细胞因子水平和 MPO 活性表明 SAP15 可有效减轻促炎反应。
这些发现表明 SAP15 是一种具有新型细胞穿透肽的新型抗炎肽,可作为 IBD 和其他炎症性疾病的治疗药物。