Zhou Lushan, Zeng Yuhan, Baker Lane A, Hou Jianghui
Department of Chemistry; Indiana University ; Bloomington, IN USA.
Department of Internal Medicine - Renal Division ; St. Louis, MO USA ; Center for Investigation of Membrane Excitability Diseases; Washington University Medical School ; St. Louis, MO USA.
Tissue Barriers. 2015 Nov 10;3(4):e1105907. doi: 10.1080/21688370.2015.1105907. eCollection 2015 Oct-Dec.
Direct recording of tight junction permeability is of pivotal importance to many biologic fields. Previous approaches bear an intrinsic disadvantage due to the difficulty of separating tight junction conductance from nearby membrane conductance. Here, we propose the design of Double whole-cell Voltage Clamp - Ion Conductance Microscopy (DVC-ICM) based on previously demonstrated potentiometric scanning of local conductive pathways. As proposed, DVC-ICM utilizes two coordinated whole-cell patch-clamps to neutralize the apical membrane current during potentiometric scanning, which in models described here will profoundly enhance the specificity of tight junction recording. Several potential pitfalls are considered, evaluated and addressed with alternative countermeasures.
紧密连接通透性的直接记录对许多生物学领域至关重要。由于难以将紧密连接电导与附近膜电导分离,以往的方法存在固有缺陷。在此,我们基于先前证明的局部传导途径的电位扫描,提出了双全细胞电压钳 - 离子电导显微镜(DVC-ICM)的设计。如所提出的,DVC-ICM利用两个协同的全细胞膜片钳在电位扫描期间中和顶膜电流,在此处描述的模型中,这将极大地提高紧密连接记录的特异性。考虑、评估了几个潜在的陷阱,并采取了替代对策加以解决。