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首页> 外文期刊>American Journal of Pathology >Failure of Pelvic Organ Support in Mice Deficient In Fibulin-3
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Failure of Pelvic Organ Support in Mice Deficient In Fibulin-3

机译:缺乏Fibulin-3的小鼠骨盆器官支持失败

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摘要

Fibulin-5 is crucial for normal elastic fiber synthesis in the vaginal wall; more than 90% of fibulin-5-knockout mice develop pelvic organ prolapse by 20 weeks of age. In contrast, fibulin-1 and -2 deficiencies do not result in similar pathologies, and fibulin-4-knockout mice die shortly after birth. EFEMP1 encodes fibulin-3, an extracellular matrix protein important in the maintenance of abdominal fascia. Herein, we evaluated the role of fibulin-3 in pelvic organ support. Pelvic organ support was impaired significantly in female Efemp1 knockout mice (Fbln3–[supi]/–), and overt vaginal, perineal, and rectal prolapse occurred in 26.9% of animals. Prolapse severity increased with age but not parity. Fibulin-5 was up-regulated in vaginal tissues from Fbln3–[supi]/– mice regardless of prolapse. Despite increased expression of fibulin-5 in the vaginal wall, pelvic organ support failure occurred in Fbln3–[supi]/– animals, suggesting that factors related to aging led to prolapse. Elastic fiber abnormalities in vaginal tissues from young Fbln3–[supi]/– mice progressed to severe elastic fiber disruption with age, and vaginal matrix metalloprotease activity was increased significantly in Fbln3–[supi]/– animals with prolapse compared with Fbln3–[supi]/– mice without prolapse. Overall, these results indicate that both fibulin-3 and -5 are important in maintaining pelvic organ support in mice. We suggest that increased vaginal protease activity and abnormal elastic fibers in the vaginal wall are important components in the pathogenesis of pelvic organ prolapse.
机译:阴道壁中,Fibulin-5对于正常的弹性纤维合成至关重要。超过90%的fibrin-5基因敲除小鼠到20周龄时会出现 盆腔器官脱垂。相比之下,fibulin-1 和-2缺陷不会导致相似的病理, fibulin-4-knockout小鼠出生后不久就死亡。 EFEMP1编码 bulbulin-3,这是一种在腹筋膜的 维护中重要的细胞外基质蛋白。在本文中,我们评估了fibulin-3在盆腔器官支持中的作用 。在雌性Efemp1基因敲除小鼠(Fbln3 – [supi / – )], 和明显的阴道,会阴和直肠中,盆腔器官的支持显着降低脱出发生在 26.9%的动物中。脱垂严重程度随年龄增长而增加,但 奇偶性没有。无论脱垂如何,Fbln3 –su // 小鼠的阴道组织中Fibulin-5均上调。尽管 fibulin-5在阴道壁中的表达增加,但Fbln3 –su // 动物中发生了盆腔器官支持失败 ,这表明与衰老相关的 因素导致脱垂。年轻的Fbln3 –su // 小鼠 的阴道组织中的弹性纤维异常 随着年龄的增长而发展为严重的弹性纤维破坏,并且 在Fbln3 –sup // 脱垂动物中,阴道基质金属蛋白酶活性显着增加 与Fbln3 小鼠没有脱垂。总体而言, 这些结果表明,fibulin-3和-5在维持小鼠骨盆器官支持中都很重要。我们建议 增加的阴道蛋白酶活性和阴道壁中异常的弹性纤维 是骨盆器官脱垂的发病机理 的重要组成部分。

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  • 来源
    《American Journal of Pathology》 |2009年第1期|206-215|共10页
  • 作者单位

    From the Department of Obstetrics and Gynecology,University of Texas Southwestern Medical Center, Dallas, Texas;

    From the Department of Obstetrics and Gynecology,University of Texas Southwestern Medical Center, Dallas, Texas;

    From the Department of Obstetrics and Gynecology,University of Texas Southwestern Medical Center, Dallas, Texas;

    From the Department of Obstetrics and Gynecology,University of Texas Southwestern Medical Center, Dallas, Texas;

    the Department of Anatomy and Cell Biology,McGill University, Montreal, Canada;

    and the Departments of Ophthalmology and Vision Science,University of Arizona, Tucson, Arizona|and Physiology,University of Arizona, Tucson, Arizona;

    From the Department of Obstetrics and Gynecology,University of Texas Southwestern Medical Center, Dallas, Texas;

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