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热敏水凝胶将生物活性蛋白输送至阴道壁。

Thermosensitive hydrogels deliver bioactive protein to the vaginal wall.

作者信息

Good Meadow M, Montoya T Ignacio, Shi Haolin, Zhou Jun, Huang YiHui, Tang Liping, Acevedo Jesus F, Word R Ann

机构信息

Division of Female Pelvic Medicine and Reconstructive Surgery, Department of Obstetrics and Gynecology, University of Texas Southwestern Medical Center, Dallas, TX, United States of America.

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States of America.

出版信息

PLoS One. 2017 Oct 26;12(10):e0186268. doi: 10.1371/journal.pone.0186268. eCollection 2017.

Abstract

The pathophysiology and natural history of pelvic organ prolapse (POP) are poorly understood. Consequently, our approaches to treatment of POP are limited. Alterations in the extracellular matrix components of pelvic support ligaments and vaginal tissue, including collagen and elastin, have been associated with the development of POP in animals and women. Prior studies have shown the protease MMP-9, a key player of ECM degradation, is upregulated in vaginal tissues from both mice and women with POP. On the other hand, fibulin-5, an elastogenic organizer, has been found to inhibit MMP-9 in the vaginal wall. Hence, we hypothesized that prolonged release of fibulin-5 may delay progression of POP. To test the hypothesis, oligo (ethylene glycol)-based thermosensitive hydrogels were fabricated, characterized and then used to deliver fibulin-5 to the vaginal wall and inhibit MMP-9 activity. The results indicate that hydrogels are cell and tissue compatible. The hydrogels also prolong the ½ life of fibulin-5 in cultured vaginal fibroblasts and in the vaginal wall in vivo. Finally, fibulin-5-containing hydrogels resulted in incorporation of fibulin-5 into the vaginal matrix and inhibition of MMP-9 for several weeks after injection. These results support the idea of fibulin-5 releasing hydrogel being developed as a new treatment for POP.

摘要

盆腔器官脱垂(POP)的病理生理学和自然病史目前尚不清楚。因此,我们治疗POP的方法有限。盆腔支持韧带和阴道组织的细胞外基质成分(包括胶原蛋白和弹性蛋白)的改变,在动物和女性中都与POP的发生有关。先前的研究表明,蛋白酶MMP - 9是细胞外基质降解的关键因子,在患有POP的小鼠和女性的阴道组织中表达上调。另一方面,弹性生成组织者纤连蛋白 - 5已被发现可抑制阴道壁中的MMP - 9。因此,我们假设纤连蛋白 - 5的持续释放可能会延缓POP的进展。为了验证这一假设,制备并表征了基于寡聚(乙二醇)的热敏水凝胶,然后将其用于向阴道壁递送纤连蛋白 - 5并抑制MMP - 9活性。结果表明水凝胶与细胞和组织具有相容性。水凝胶还延长了纤连蛋白 - 5在培养的阴道成纤维细胞和体内阴道壁中的半衰期。最后,含纤连蛋白 - 5的水凝胶在注射后数周内导致纤连蛋白 - 5掺入阴道基质并抑制MMP - 9。这些结果支持了将纤连蛋白 - 5释放水凝胶开发为POP新疗法的想法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d9c/5657977/ce6f84d561f9/pone.0186268.g001.jpg

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