Bloom Adam K, Samsom Michael L, Regmi Suresh C, Steele Bridgett L, Schmidt Tannin A
Biomedical Engineering Graduate Program, University of Calgary, Calgary, AB, Canada.
Faculty of Kinesiology, KNB 426, 2500 University Dr. NW, University of Calgary, Calgary, AB, T2N 1N4, Canada.
BMC Musculoskelet Disord. 2019 Feb 26;20(1):93. doi: 10.1186/s12891-019-2469-4.
The objective of this study was to use confocal fluorescence recovery after photobleaching (FRAP) to examine the specific and dose-dependent effect of proteoglycan 4 (PRG4) on hyaluronan (HA) solutions of different molecular weight; and assess the effect of reduction and alkylation (R/A) of PRG4 on its effects on HA solutions.
Confocal FRAP was used to determine the diffusion coefficient of fluorescein isothiocyanate (FITC)-dextran tracer (D) through 1500 kDa and 500 kDa HA solutions (0-3.3 mg/ml) ± PRG4 or a control protein, bovine serum albumin (BSA), at physiological (450 μg/ml) or pathophysiological (45 μg/ml) concentrations. The effect of PRG4 or R/A PRG4 on 1500 kDa HA solutions was also investigated. Empirical constants obtained from fitting data to the universal scaling equation were used to calculate the average distribution of apparent mesh sizes.
PRG4 at both 45 and 450 μg/ml slowed the diffusion of the FITC-dextran tracer for all concentrations of HA and caused a decrease in the apparent mesh size within the HA solution. This effect was specific to PRG4, not observed with BSA, but not dependent on its tertiary/quaternary structure as the effect remained after R/A of PRG4.
These results demonstrate that PRG4 can significantly alter the solution properties of HA; PRG4 essentially reduced the permeability of the HA network. This effect may be due to PRG4 entangling HA molecules through binding and/or HA crowding PRG4 molecules into a self-assembled network. Collectively these findings contribute to the understanding of PRG4 and HA interaction(s) in solution and therefore the function of SF in diarthroidal joints.
本研究的目的是利用共聚焦光漂白后荧光恢复技术(FRAP),研究蛋白聚糖4(PRG4)对不同分子量透明质酸(HA)溶液的特异性和剂量依赖性影响;并评估PRG4的还原和烷基化(R/A)对其在HA溶液中作用的影响。
采用共聚焦FRAP技术,测定异硫氰酸荧光素(FITC)-葡聚糖示踪剂(D)在1500 kDa和500 kDa HA溶液(0 - 3.3 mg/ml)中±PRG4或对照蛋白牛血清白蛋白(BSA)的扩散系数,PRG4或BSA的浓度为生理浓度(450 μg/ml)或病理生理浓度(45 μg/ml)。还研究了PRG4或R/A PRG4对1500 kDa HA溶液的影响。将数据拟合到通用标度方程得到的经验常数用于计算表观网孔尺寸的平均分布。
45 μg/ml和450 μg/ml的PRG4均减缓了所有浓度HA溶液中FITC -葡聚糖示踪剂的扩散,并导致HA溶液中表观网孔尺寸减小。这种效应是PRG4特有的,在BSA中未观察到,但不依赖于其三级/四级结构,因为PRG4经R/A处理后该效应仍然存在。
这些结果表明,PRG4可显著改变HA的溶液性质;PRG4本质上降低了HA网络的通透性。这种效应可能是由于PRG4通过结合使HA分子缠结和/或HA将PRG4分子聚集到自组装网络中。这些发现共同有助于理解溶液中PRG4与HA的相互作用,进而有助于理解滑膜液在滑膜关节中的功能。