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MT-100是一种人源Tie2激动性抗体,可通过新靶点Srpx2改善糖尿病小鼠的阴茎神经血管系统。

MT-100, a human Tie2-agonistic antibody, improves penile neurovasculature in diabetic mice via the novel target Srpx2.

作者信息

Liu Fang-Yuan, Cho Young-Lai, Fridayana Fitri Rahma, Niloofar Lashkari, Vo Minh Nhat, Huang Yan, Limanjaya Anita, Kwon Mi-Hye, Ock Jiyeon, Lee Seon-Jin, Yin Guo Nan, Lee Nam-Kyung, Ryu Ji-Kan

机构信息

National Research Center for Sexual Medicine and Department of Urology, Inha University College of Medicine, Incheon, Republic of Korea.

Environmental Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Republic of Korea.

出版信息

Exp Mol Med. 2025 Feb;57(1):104-117. doi: 10.1038/s12276-024-01373-1. Epub 2025 Jan 1.

Abstract

Diabetes is an incurable, chronic disease that can lead to many complications, including angiopathy, peripheral neuropathy, and erectile dysfunction (ED). The angiopoietin-Tie2 signaling pathway plays a critical role in blood vessel development, formation, remodeling, and peripheral nerve regeneration. Therefore, strategies for activating the Tie2 signaling pathway have been developed as potential therapies for neurovascular diseases. Here, we developed a human Tie2-agonistic antibody (MT-100) that not only resists Ang-2 antagonism and activates Tie2 signaling but also regulates a novel target, sushi repeat-containing protein X-linked 2 (Srpx2). This regulation led to the survival of vascular and neuronal cells, a reduction in the production of reactive oxygen species (ROS), activation of the PI3K/AKT/eNOS signaling pathway, increased expression of neurotrophic factors, and ultimately alleviation of ED in diabetic mice. Our findings not only provide conclusive evidence that MT-100 is a promising therapeutic strategy for the treatment of diabetic ED but also suggest it has substantial clinical applications for other complications associated with diabetes.

摘要

糖尿病是一种无法治愈的慢性疾病,可导致多种并发症,包括血管病变、周围神经病变和勃起功能障碍(ED)。血管生成素-Tie2信号通路在血管发育、形成、重塑和周围神经再生中起关键作用。因此,激活Tie2信号通路的策略已被开发为神经血管疾病的潜在治疗方法。在此,我们开发了一种人Tie2激动性抗体(MT-100),它不仅能抵抗Ang-2的拮抗作用并激活Tie2信号,还能调节一个新的靶点,即含寿司重复序列蛋白X连锁2(Srpx2)。这种调节导致血管和神经细胞的存活,活性氧(ROS)产生减少,PI3K/AKT/eNOS信号通路激活,神经营养因子表达增加,最终减轻糖尿病小鼠的ED。我们的研究结果不仅提供了确凿证据,证明MT-100是治疗糖尿病性ED的一种有前景的治疗策略,还表明它在糖尿病相关的其他并发症方面具有重要的临床应用价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8492/11799434/a14e2fa940fa/12276_2024_1373_Fig1_HTML.jpg

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