Dodd S, Place G A, Hall R L, Harding S E
School of Biological Sciences, University of Nottingham, UK.
Eur Biophys J. 1999;28(1):38-47. doi: 10.1007/s002490050181.
We have used two different approaches to determine hydrodynamic parameters for mucins secreted by guinea-pig tracheal epithelial cells in primary culture. Cells were cultured under conditions that promote mucous cell differentiation. Secreted mucins were isolated as the excluded fraction from a Sepharose CL-4B gel filtration column run under strongly dissociating conditions. Biochemical analysis confirmed the identity of the high molecular weight material as mucins. Analytical ultracentrifugation was used to study the physical properties of the purified mucins. The weight average molecular mass (Mw) for three different preparations ranged from 3.3 x 10(6) to 4.7 x 10(6) g/mol (corresponding to an average structure of 1-2 subunits), and the sedimentation coefficient from 25.5 to 35 S. Diffusion coefficients ranging from 4.5 x 10(-8) to 6.4 x 10(-8) cm2/s were calculated using the Svedberg equation. A polydispersity index (Mz/Mw) of approximately 1.4 was obtained. Diffusivity values were also determined by image analysis of mucin granule exocytosis captured by videomicroscopy. The time course of hydration and dissolution of mucin was measured and a relationship is presented which models both phases, each with first order kinetics, in terms of a maximum radius and rate constants for hydration and dissolution. A median diffusivity value of 8.05 x 10(-8) cm2/s (inter-quartile range = 1.11 x 10(-7) to 6.08 x 10(-8) cm2/sec) was determined for the hydration phase. For the dissolution phase, a median diffusivity value of 6.98 x 10(-9) cm2/s (inter-quartile range = 1.47 x 10(-8) to 3.25 x 10(-9) cm2/sec) was determined. These values were compared with the macromolecular diffusion coefficients (D20,w) obtained by analytical ultracentrifugation. When differences in temperature and viscosity were taken into account, the resulting D37,g was within the range of diffusivity values for dissolution. Our findings show that the physicochemical properties of mucins secreted by cultured guinea-pig tracheal epithelial cells are similar to those of mucins of the single or double subunit type purified from respiratory mucus or sputum. These data also suggest that measurement of the diffusivity of dissolution may be a useful means to estimate the diffusion coefficient of mucins in mucus gel at the time of exocytosis from a secretory cell.
我们采用了两种不同的方法来测定原代培养的豚鼠气管上皮细胞分泌的粘蛋白的流体动力学参数。细胞在促进粘液细胞分化的条件下培养。分泌的粘蛋白在强解离条件下通过琼脂糖CL - 4B凝胶过滤柱作为排阻级分被分离出来。生化分析证实了高分子量物质为粘蛋白。使用分析超速离心法研究纯化粘蛋白的物理性质。三种不同制剂的重均分子量(Mw)范围为3.3×10⁶至4.7×10⁶ g/mol(对应于1 - 2个亚基的平均结构),沉降系数为25.5至35 S。使用斯维德伯格方程计算得到的扩散系数范围为4.5×10⁻⁸至6.4×10⁻⁸ cm²/s。获得了约为1.4的多分散指数(Mz/Mw)。扩散率值也通过视频显微镜捕获的粘蛋白颗粒胞吐作用的图像分析来确定。测量了粘蛋白水合和溶解的时间进程,并给出了一个关系模型,该模型根据水合和溶解的最大半径和速率常数对两个阶段进行建模,每个阶段均为一级动力学。水合阶段的中位扩散率值为8.05×10⁻⁸ cm²/s(四分位间距 = 1.11×10⁻⁷至6.08×10⁻⁸ cm²/sec)。对于溶解阶段,中位扩散率值为6.98×10⁻⁹ cm²/s(四分位间距 = 1.47×10⁻⁸至3.25×10⁻⁹ cm²/sec)。将这些值与通过分析超速离心法获得的大分子扩散系数(D20,w)进行比较。考虑到温度和粘度的差异后,得到的D37,g在溶解扩散率值范围内。我们的研究结果表明,培养的豚鼠气管上皮细胞分泌的粘蛋白的物理化学性质与从呼吸道粘液或痰液中纯化的单亚基或双亚基类型的粘蛋白相似。这些数据还表明,测量溶解扩散率可能是估计分泌细胞胞吐时粘蛋白在粘液凝胶中的扩散系数的一种有用方法。