Couri Bruna M, Lenis Andrew T, Borazjani Ali, Balog Brian M, Kuang Mei, Butler Robert S, Penn Marc S, Damaser Margot S
From the Departments of *Obstetrics and Gynecology and †Biomedical Engineering, Cleveland Clinic, Cleveland, OH; ‡Department of Urology, University of California Los Angeles, Los Angeles, CA; and §Chemical and Biomedical Engineering, Cleveland State University; and ∥Advanced Platform Technology Center, Louis Stokes VA Medical Center, Cleveland; ¶Department of Biology, University of Akron, Akron; #Department of Quantitative Health Sciences, Cleveland Clinic, Cleveland; **Department of Integrative Medical Sciences, Northeast Ohio University College of Medicine, Rootstown; ††Summa Cardiovascular Institute, Summa Health System, Akron; and ‡‡Glickman Urological & Kidney Institute, Cleveland Clinic, Cleveland, OH.
Female Pelvic Med Reconstr Surg. 2017 Nov/Dec;23(6):449-456. doi: 10.1097/SPV.0000000000000394.
The aim of this study was to determine the effect of pregnancy and delivery mode on cytokine expression in the pelvic organs and serum of lysyl oxidase like-1 knockout (LOXL1 KO) mice, which develop pelvic organ prolapse after delivery.
Bladder, urethra, vagina, rectum, and blood were harvested from female LOXL1 KO mice during pregnancy, after vaginal or cesarean delivery, and from sham cesarean and unmanipulated controls. Pelvic organs and blood were also harvested from pregnant and vaginally delivered wild-type (WT) mice and from unmanipulated female virgin WT controls. Specimens were assessed using quantitative real-time reverse transcription polymerase chain reaction and/or enzyme-linked immunosorbent assay.
Both CXCL12 and CCL7 mRNA were significantly up-regulated in the vagina, urethra, bladder, and rectum of pregnant LOXL1 KO mice compared with pregnant WT mice, suggesting systemic dysregulation of both of these cytokines in LOXL1 KO mice as a response to pregnancy.The differences in cytokine expression between LOXL1 KO and WT mice in pregnancy persisted after vaginal delivery. CCL7 gene expression increases faster and to a greater extent in LOXL1 KO mice, translating to longer lasting increases in CCL7 in serum of LOXL1 KO mice after vaginal delivery, compared with pregnant mice.
Lysyl oxidase like-1 KO mice have an increased cytokine response to pregnancy perhaps because they are less able to reform and re-cross-link stretched elastin to accommodate pups, and this resultant tissue stretches during pregnancy. The up-regulation of CCL7 after delivery could provide an indicator of level of childbirth injury, to which the urethra and vagina seem to be particularly vulnerable.
本研究旨在确定妊娠和分娩方式对赖氨酰氧化酶样1基因敲除(LOXL1 KO)小鼠盆腔器官和血清中细胞因子表达的影响,这类小鼠在分娩后会发生盆腔器官脱垂。
在妊娠期间、经阴道或剖宫产分娩后,从雌性LOXL1 KO小鼠采集膀胱、尿道、阴道、直肠和血液样本,并采集假剖宫产和未处理的对照小鼠样本。还从妊娠和经阴道分娩的野生型(WT)小鼠以及未处理的雌性未孕WT对照小鼠采集盆腔器官和血液样本。使用定量实时逆转录聚合酶链反应和/或酶联免疫吸附测定对样本进行评估。
与妊娠WT小鼠相比,妊娠LOXL1 KO小鼠的阴道、尿道、膀胱和直肠中CXCL12和CCL7 mRNA均显著上调,这表明LOXL1 KO小鼠中这两种细胞因子出现系统性失调,作为对妊娠的一种反应。阴道分娩后,妊娠的LOXL1 KO小鼠和WT小鼠之间细胞因子表达的差异仍然存在。与妊娠小鼠相比,LOXL1 KO小鼠中CCL7基因表达增加得更快且程度更大,这导致阴道分娩后LOXL1 KO小鼠血清中CCL7的增加持续时间更长。
赖氨酰氧化酶样1基因敲除小鼠对妊娠的细胞因子反应增强,可能是因为它们在重塑和重新交联拉伸的弹性蛋白以容纳幼崽方面能力较弱,并且由此产生的组织在妊娠期间会伸展。分娩后CCL7的上调可能提供分娩损伤程度的一个指标,尿道和阴道似乎对此特别敏感。