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胸腺肽β-4 - 一种治疗成年哺乳动物中耳损伤的潜在工具。

Thymosin beta-4 - A potential tool in healing middle ear lesions in adult mammals.

机构信息

Department of Otorhinolaryngology, Head and Neck Surgery, University of Pecs, Medical School, H-7624 Pecs, Hungary.

Szentagothai Research Centre, University of Pecs, H-7624 Pecs, Hungary.

出版信息

Int Immunopharmacol. 2023 Mar;116. doi: 10.1016/j.intimp.2023.109830. Epub 2023 Feb 14.

Abstract

Acute tympanic membrane perforations primarily occur due to injury or infection in humans. In acute cases, nearly 80-94 % of the perforations heal spontaneously. In chronic cases, non-surgical treatment becomes significantly limited, and the perforation can be restored only by myringoplasty. In addition to classical grafts such as the fascia or cartilage, promising results have been reported with various biological materials including silk or acellular collagen. However, despite of all the efforts, healing remains insufficient. Consequentially, a need for substances which actively promote tympanic cell migration and proliferation is deemed essential. In our study, we utilized Thymosin beta-4 (TB4), a 43aa peptide possessing many regenerative properties in various organ systems. Our aim was to reveal the impact of externally administered TB4 regarding impairments of the middle ear, particularly the tympanic membrane. We harvested tympanic membranes from adult mice and treated these with TB4 or PBS on both collagen gel matrixes and in the form of floating, ex vivo explants. Cell migration and proliferation was measured, while immunocytochemical analyses were performed to determine cell type and the nature of the targeted molecules. We discovered the peptide affects the behavior of epidermal and epithelial cells of the tympanic membrane in vitro. Moreover, as our initial results imply, it is not the differentiated, yet most likely the local epidermal progenitor cells which are the primary targets of the molecule. Our present results unveil a new, thus far undiscovered field regarding clinical utilization for TB4 in the future.

摘要

急性鼓膜穿孔主要由人类的损伤或感染引起。在急性病例中,近 80-94%的穿孔会自发愈合。在慢性病例中,非手术治疗的效果显著受限,只有通过鼓膜成形术才能修复穿孔。除了筋膜或软骨等经典移植物外,各种生物材料,如丝或去细胞胶原,也已报道取得了有前景的效果。然而,尽管付出了所有努力,愈合仍然不足。因此,人们认为需要一些能够积极促进鼓膜细胞迁移和增殖的物质。在我们的研究中,我们利用了胸腺素β-4(TB4),这是一种 43 个氨基酸的肽,在各种器官系统中具有许多再生特性。我们的目的是揭示外源性 TB4 对中耳,特别是鼓膜的损伤的影响。我们从成年小鼠中采集鼓膜,并在胶原凝胶基质上和作为游离的、离体的外植体上用 TB4 或 PBS 处理这些外植体。测量细胞迁移和增殖,并进行免疫细胞化学分析以确定细胞类型和靶向分子的性质。我们发现该肽在体外影响鼓膜的表皮和上皮细胞的行为。此外,正如我们的初步结果所暗示的,受该分子影响的主要是未分化的、但很可能是局部表皮祖细胞,而不是已分化的细胞。我们目前的结果揭示了一个新的、迄今为止尚未被发现的领域,即未来 TB4 在临床应用中的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b62a/11068331/5393289cf022/nihms-1936854-f0001.jpg

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