Department of Andrology and Urology, Changzhou TCM Hospital, Changzhou, 213000, Jiangsu Province, China.
Department of Urology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200080, China.
Lasers Med Sci. 2019 Aug;34(6):1217-1227. doi: 10.1007/s10103-018-02713-0. Epub 2019 Feb 22.
This research aims to observe and compare the wound healing process of urethral bladder after transurethral holmium laser resection of bladder tumor (HoLRBT) and transurethral resection of bladder tumor (TURBT) and explore the possible mechanism of wound healing and bladder re-epithelialization after HoLRBT. An animal model of canine achieving HoLRBT and TURBT was established. Cystoscopy was performed at different time points (3 days and 1, 2, 3, and 4 weeks) after operation to observe the wound healing and re-epithelialization of bladder epithelium. Bladder mucosa specimens were obtained and histopathological changes of the bladder epithelium were observed under light microscope after HE staining. Immunochemistry was used to determine the cell expression ofCK5, CK14, EGF, EGFR; microRNA expressions of CK5, CK14, EGF, and EGFR were measured by qRT-PCR. The changes of urinary EGF concentration were detected by ELISA. The bladder epithelial wound was repaired and re-epithelialized at 1 week after HoLRBT. At the 4th week, the bladder wound was basically completed and re-epithelialized; repair of bladder epithelial wounds recapitulates the wounds with the proliferation and migration of residual epithelial cells under the wound and the bladder epithelium that proliferates alongside the wound surface to complete re-epithelialization. The process begins at 1 week after surgery and basically completes at 4 weeks after surgery. CK5 and CK14 positive cells were detected in the basal cells of the bladder epithelium after HoLRBT, and the expression of CK5 and CK14 mRNA in the basal cells of the bladder epithelium under hyperplasia was significantly higher than that of the normal bladder epithelial basal cells. Bladder epithelial wound repair of TURBT group was performed by the proliferative differentiation of the peri-bladder epithelium adjacent to the wound edge and crawled to the wound surface to complete the re-epithelialization process. The wound repair and re-epithelialization were significantly slower than HoLRBT group. The CK5 and CK14 positive cells can also be detected in the basal cells of marginal hyperplasia of basal margin, and the expression of CK5 and CK14 mRNA in the basal cells of the peri-bladder hyperplasia is obviously higher than that of the normal bladder epithelial basal cells. The expression of EGF in bladder regenerating epithelium gradually increased with time after HoLRBT. Bladder basal cells and bladder regenerating epithelium express high levels of EGFR after HoLRBT. The concentration of EGF in urine after HoLRBT and TURBT increased significantly after surgery, and peaked at 3 days after operation. The urinary EGF concentration in HoLRBT group was higher than that in TURBT group at 3 and 4 weeks after operation. The re-epithelialization process can be seen 1 week after the cystectomy with holmium laser cystectomy, and the epithelialization rate is faster than the traditional transection surgery. This is because the residual bladder epithelial stem cells and wound marginal epithelial cells are involved in the process of wound repair and re-epithelialization following HoLRBT. But only the marginal epithelial tissue participates in the re-epithelialization process after TURBT, so the repair rate of TURBT is slower. The repair of bladder epithelium after HoLRBT is related to the stimulation of tissue factor EGF. The regenerated bladder epithelium also participates in the wound repair process by means of autocrine of EGF.
本研究旨在观察和比较经尿道钬激光膀胱肿瘤切除术(HoLRBT)和经尿道膀胱肿瘤切除术(TURBT)后尿道膀胱的愈合过程,并探讨 HoLRBT 后伤口愈合和膀胱再上皮化的可能机制。建立了犬 HoLRBT 和 TURBT 的动物模型。术后不同时间点(3 天和 1、2、3 和 4 周)进行膀胱镜检查,观察膀胱上皮的愈合和再上皮化。HE 染色后,取膀胱黏膜标本,观察膀胱上皮的光镜下组织学变化。采用免疫组织化学法检测 CK5、CK14、EGF、EGFR 的细胞表达;采用 qRT-PCR 法检测 CK5、CK14、EGF、EGFR 的 microRNA 表达;采用 ELISA 法检测尿 EGF 浓度变化。HoLRBT 后 1 周膀胱上皮伤口修复并再上皮化,第 4 周膀胱伤口基本完成并再上皮化;膀胱上皮伤口修复再上皮化过程是在伤口下残余上皮细胞增殖和迁移的基础上进行的,同时沿伤口表面增殖的膀胱上皮完成再上皮化。该过程始于术后 1 周,基本在术后 4 周完成。HoLRBT 后膀胱上皮基底层可见 CK5 和 CK14 阳性细胞,膀胱上皮基底层 CK5 和 CK14 mRNA 的表达明显高于正常膀胱上皮基底层。TURBT 组膀胱上皮伤口修复是通过伤口边缘邻近的膀胱上皮的增殖分化并爬行到伤口表面完成再上皮化过程。其伤口修复和再上皮化明显慢于 HoLRBT 组。边缘增生的基底层也可检测到 CK5 和 CK14 阳性细胞,基底层增生的 CK5 和 CK14 mRNA 表达明显高于正常膀胱上皮基底层。HoLRBT 后膀胱再生上皮中 EGF 的表达随时间逐渐增加。HoLRBT 后膀胱基底层细胞和膀胱再生上皮高表达 EGFR。HoLRBT 和 TURBT 术后尿中 EGF 浓度明显升高,术后 3 天达峰值。HoLRBT 组术后 3 周和 4 周尿 EGF 浓度均高于 TURBT 组。HoLRBT 后 1 周即可观察到膀胱切除术的上皮化过程,上皮化速度快于传统的横断手术。这是因为 HoLRBT 后,残余膀胱上皮干细胞和伤口边缘上皮细胞参与了伤口修复和再上皮化过程。但 TURBT 后仅边缘上皮组织参与再上皮化过程,因此 TURBT 的修复速度较慢。HoLRBT 后膀胱上皮的修复与组织因子 EGF 的刺激有关。再生的膀胱上皮也通过 EGF 的自分泌参与伤口修复过程。