Dzekunov S M, Spring K R
Laboratory of Kidney and Electrolyte Metabolism, National Heart, Lung and Blood Institute, National Institues of Health, Building 10, Room 6N260, 10 Center Dr., MSC 1603, Bethesda, MD 20892-1603, USA.
J Membr Biol. 1998 Nov 1;166(1):9-14. doi: 10.1007/s002329900443.
The lateral intercellular spaces (LIS) of MDCK cell epithelia grown on permeable supports are about 0.4 pH units acidic to the bathing solutions, presumably because of buffering by the fixed negative charges on the surface of the lateral cell membranes. To test the hypothesis that fixed buffers are responsible for the acidity, a theoretical and experimental approach was developed for the determination of the concentration and pK of the fixed buffer constituted by the glycocalyx. The pH of the solution in the LIS was measured by ratiometric fluorescence microscopy while the buffer concentration or composition of the bathing solutions was altered. In addition, the divalent cation Sr2+ was added to the perfusion solutions to displace protons from the fixed buffer sites for the determination of the fixed buffer properties. We conclude that the LIS contain 3.7 mm of pK 6.2 fixed buffer and that this buffer is responsible for the acidic microenvironment in the LIS.
生长在可渗透支持物上的MDCK细胞上皮的外侧细胞间隙(LIS)比外部浴液的酸性约高0.4个pH单位,这大概是由于外侧细胞膜表面的固定负电荷的缓冲作用。为了验证固定缓冲剂导致酸性的假说,开发了一种理论和实验方法来测定由糖萼构成的固定缓冲剂的浓度和pK值。通过比率荧光显微镜测量LIS中溶液的pH值,同时改变外部浴液的缓冲剂浓度或成分。此外,向灌注溶液中添加二价阳离子Sr2+,以从固定缓冲位点置换质子,从而确定固定缓冲剂的性质。我们得出结论,LIS含有3.7 mM、pK为6.2的固定缓冲剂,并且这种缓冲剂导致了LIS中的酸性微环境。