Choi Bo-Hwa, You Sungyong, Park Chang-Shin, Cho Eun-Ho, Park Taeeun D, Kim Sungsoo, Kim Young-Ju, Lee Tack, Kim Jayoung
a Department of Pharmacology , Hypoxia-Related Disease Research Center, Inha Research Institute for Medical Sciences, Inha University College of Medicine , Incheon , South Korea.
b Departments of Surgery and Biomedical Sciences , Cedars-Sinai Medical Center , Los Angeles , CA , USA.
Cell Cycle. 2017 Apr 18;16(8):749-758. doi: 10.1080/15384101.2017.1295184. Epub 2017 Feb 22.
Interstitial cystitis (IC) is a chronic bladder dysfunction characterized as urinary frequency, urgency, nocturia, and pelvic pain. The changes in urethra may wind up with the bladder changes in structure and functions, however, the functions of the urethra in IC remains elusive. The aim of this study was to understand the perturbed gene expression in urethra, compared with urinary bladder, associated with the defected urodynamics. Using female IC mimic rats, a comprehensive RNA-sequencing combined with a bioinformatics analysis was performed and revealed that IC-specific genes in bladder or urethra. Gene ontology analysis suggested that the cell adhesion or extracellular matrix regulation, intracellular signaling cascade, cardiac muscle tissue development, and second messenger-mediated signaling might be the most enriched cellular processes in IC context. Further study of the effects of these bladder- or urethra-specific genes may suggest underlying mechanism of lower urinary tract function and novel therapeutic strategies against IC.
间质性膀胱炎(IC)是一种慢性膀胱功能障碍,其特征为尿频、尿急、夜尿症和盆腔疼痛。尿道的变化最终可能导致膀胱结构和功能的改变,然而,IC中尿道的功能仍不清楚。本研究的目的是了解与尿动力学缺陷相关的、与膀胱相比尿道中基因表达的扰动情况。使用雌性IC模拟大鼠,进行了全面的RNA测序并结合生物信息学分析,揭示了膀胱或尿道中的IC特异性基因。基因本体分析表明,细胞粘附或细胞外基质调节、细胞内信号级联、心肌组织发育和第二信使介导的信号传导可能是IC背景下最丰富的细胞过程。对这些膀胱或尿道特异性基因作用的进一步研究可能揭示下尿路功能的潜在机制以及针对IC的新治疗策略。