Edsfeldt Sara, Holm Björn, Mahlapuu Margit, Reno Carol, Hart David A, Wiig Monica
a Department of Surgical Sciences, Hand Surgery , Uppsala University , Uppsala , Sweden.
b Department of Hand Surgery , Uppsala University Hospital , Uppsala , Sweden.
Ups J Med Sci. 2017 Mar;122(1):28-34. doi: 10.1080/03009734.2016.1230157. Epub 2016 Sep 23.
To investigate the anti-adhesive mechanisms of PXL01 in sodium hyaluronate (HA) by using the rabbit lactoferrin peptide, rabPXL01 in HA, in a rabbit model of healing tendons and tendon sheaths. The mechanism of action for PXL01 in HA is interesting since a recent clinical study of the human lactoferrin peptide PXL01 in HA administered around repaired tendons in the hand showed improved digit mobility.
On days 1, 3, and 6 after tendon injury and surgical repair, reverse transcriptase-quantitative polymerase chain reaction (RT-qPCR) was used to assess mRNA expression levels for genes encoding the mucinous glycoprotein PRG4 (also called lubricin) and a subset of matrix proteins, cytokines, and growth factors involved in flexor tendon repair. RabPXL01 in HA was administered locally around the repaired tendons, and mRNA expression was compared with untreated repaired tendons and tendon sheaths.
We observed, at all time points, increased expression of PRG4 mRNA in tendons treated with rabPXL01 in HA, but not in tendon sheaths. In addition, treatment with rabPXL01 in HA led to repression of the mRNA levels for the pro-inflammatory mediators interleukin (IL)-1β, IL-6, and IL-8 in tendon sheaths.
RabPXL01 in HA increased lubricin mRNA production while diminishing mRNA levels of inflammatory mediators, which in turn reduced the gliding resistance and inhibited the adhesion formation after flexor tendon repair.
通过在兔肌腱和腱鞘愈合模型中使用透明质酸钠(HA)中的兔乳铁蛋白肽rabPXL01,研究PXL01在HA中的抗粘连机制。PXL01在HA中的作用机制很有趣,因为最近一项关于人乳铁蛋白肽PXL01在手部修复肌腱周围注射HA的临床研究显示手指活动度有所改善。
在肌腱损伤和手术修复后的第1、3和6天,使用逆转录定量聚合酶链反应(RT-qPCR)评估编码黏液糖蛋白PRG4(也称为润滑素)以及参与屈肌腱修复的基质蛋白、细胞因子和生长因子子集的基因的mRNA表达水平。将HA中的rabPXL01局部注射到修复后的肌腱周围,并将mRNA表达与未治疗的修复肌腱和腱鞘进行比较。
我们观察到,在所有时间点,HA中rabPXL01处理的肌腱中PRG4 mRNA表达增加,但腱鞘中未增加。此外,HA中rabPXL01处理导致腱鞘中促炎介质白细胞介素(IL)-1β、IL-6和IL-8的mRNA水平受到抑制。
HA中的rabPXL01增加了润滑素mRNA的产生,同时降低了炎症介质的mRNA水平,这反过来又降低了滑动阻力并抑制了屈肌腱修复后的粘连形成。