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An inflammatory memory and angiogenic self-assembling nanofiber hydrogel scaffold seeded with Akkermansia muciniphila to accelerate the healing of diabetic ischemic ulcers

机译:一种炎症记忆和血管生成的自组装纳米纤维水凝胶支架,植入黏液阿克曼(Akkermansia muciniphila),可加速糖尿病性缺血性溃疡的愈合

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Refractory ulcers are a major challenge in the treatment of a diabetic foot, because of the immunodeficient, ischemic and high-glucose microenvironment. Inflammatory memory peptides, which were extracted from the immune mediator absent in melanoma 2 (AIM2), could effectively improve the immunodeficient microenvironment and special angiogenic peptides could effectively promote angiogenesis. Moreover, the gut flora Akkermansia muciniphila ( A. muciniphila ) participates in diabetic metabolism and could decrease high-glucose levels. In this research, a polypeptide skeleton (PPS) was synthesized based on 3,4-dihydroxyphenylalanine (DOPA) and peptides, forming the hydrophilic and hydrophobic parts. Inflammatory memory peptides and angiogenic peptides were synthesized and conjugated with the PPS, which then formed an anisotropic hydrogel through the self-assembling of β-sheet peptides based on hydrophobicity and DOPA oxidation. A. muciniphila was seeded into the hydrogel and transported into diabetic ischemic ulcers through subcutaneous injection, and the healing of diabetic ischemic ulcers was promoted. The inflammatory memory peptides were released based on the A. muciniphila enzyme response, and they firstly improved the immunity of the local surroundings. Then, the angiogenic peptides were also released through irradiation and they promoted angiogenesis. Additionally, the transported A. muciniphila could decrease the local glucose levels and spontaneously regress once the diabetic ischemic ulcers had healed. A. muciniphila combined with a functional polypeptide hydrogel may be a novel strategy for diabetic ischemic ulcer treatment.
机译:由于免疫缺陷,局部缺血和高糖微环境,难治性溃疡是治疗糖尿病足的主要挑战。从黑色素瘤2(AIM2)中不存在的免疫介质中提取的炎症记忆肽可以有效改善免疫缺陷的微环境,特殊的血管生成肽可以有效地促进血管生成。此外,肠道菌群Akkermansia muciniphila(A. muciniphila)参与糖尿病的代谢,并可能降低高糖水平。在这项研究中,基于3,4-二羟基苯丙氨酸(DOPA)和肽合成了多肽骨架(PPS),形成了亲水和疏水部分。合成了炎症记忆肽和血管生成肽并将其与PPS偶联,然后基于疏水性和DOPA氧化作用通过β-sheet肽的自组装形成各向异性的水凝胶。通过皮下注射将黏液曲霉接种到水凝胶中并转运到糖尿病性缺血性溃疡中,从而促进了糖尿病性缺血性溃疡的愈合。炎症记忆肽是基于粘液曲霉酶反应释放的,它们首先提高了局部环境的免疫力。然后,血管生成肽也通过辐射释放,并促进血管生成。另外,一旦糖尿病性缺血性溃疡愈合,所运输的粘液曲霉可降低局部葡萄糖水平并自发消退。黏液曲霉与功能性多肽水凝胶的结合可能是糖尿病性缺血性溃疡治疗的新策略。

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