Haas H G, Meyer R, Einwächter H M, Stockem W
Pflugers Arch. 1983 Dec;399(4):321-35. doi: 10.1007/BF00652760.
Passive electrical parameters of bullfrog atrial trabeculae were measured in a single gap arrangement. Attention was focussed on the resistance of internal longitudinal pathway. The influence of external Ca2+ depletion was tested using EGTA as chelating agent. Morphometry of trabeculae, fine structure of junctional complexes, and distribution of membrane-bound Ca were investigated by light and electron microscopic methods. The specific internal resistance to longitudinal current flow was 523 omega cm with normal Ringer as perfusing fluid and 1140 omega cm in EGTA-containing solution. These values are considered to represent the sum of myoplasmic and junctional resistivity. Morphometrical studies indicated an interstitial space of 12%, a mean cell length of 358 micron, and a mean cell diameter of 3.2 micron. In freeze-fractured preparations junctional structures were observed in the form of "atypical gap junctions" consisting of 10 nm particles arranged in a circular or linear array. The number of gap junctions was estimated to range between 20 and 50/cell which is equivalent to a junctional area of 0.01 or 0.03% of total surface area. A mean number of 55 particles/gap junction was calculated. After 20 min of exposure to EGTA the majority of junctional complexes were converted to clusters; the number of particles/gap junction was not significantly altered. The fluorescent dye CTC was used as a probe for membrane-bound Ca of isolated living cells. In normal Ringer a strong fluorescence was seen at the cell surface and in different intracellular compartments. With EGTA both superficial and internal fluorescence disappeared completely. From a combination of electrical and morphometrical data the resistance of intercellular junctions was calculated. Under normal conditions the specific resistance of junctional membrane amounted to 0.4 omega cm2 and the resistance of an individual connection was of the order of 10(11) omega. With EGTA, the respective values were increased by about 230%. The mechanism underlying this depression of junctional conductance is not clear. It seems not related to a rise of cytoplasmic free Ca2+. The EGTA-induced increase in internal resistance was reflected by a decrease of the length constant of a bundle. The nature of "atypical gap junctions" and their relation to tight junctions are discussed. It is concluded that the junctions observed in frog atrial muscle are analogous to gap junctions of insect or mammalian cells in spite of the different size and arrangement of the particles. A theoretical model is presented for the electrical behaviour of a bundle in a single gap arrangement.(ABSTRACT TRUNCATED AT 400 WORDS)
采用单间隙排列方式测量牛蛙心房肌小梁的被动电参数。重点关注内部纵向通路的电阻。使用乙二醇双四乙酸(EGTA)作为螯合剂测试细胞外钙耗竭的影响。通过光学显微镜和电子显微镜方法研究小梁的形态计量学、连接复合体的精细结构以及膜结合钙的分布。以正常任氏液作为灌注液时,纵向电流流动的比内阻为523Ω·cm,在含EGTA的溶液中为1140Ω·cm。这些值被认为代表了肌浆和连接部位电阻率的总和。形态计量学研究表明,细胞间隙为12%,平均细胞长度为358μm,平均细胞直径为3.2μm。在冷冻断裂标本中,观察到连接结构呈“非典型缝隙连接”形式,由排列成圆形或线性阵列的10nm颗粒组成。估计每个细胞的缝隙连接数量在20到50个之间,相当于总表面积的0.01%或0.03%。计算得出每个缝隙连接的平均颗粒数为55个。暴露于EGTA 20分钟后,大多数连接复合体转变为簇状;每个缝隙连接的颗粒数量没有显著改变。荧光染料CTC用作分离活细胞中膜结合钙的探针。在正常任氏液中,在细胞表面和不同的细胞内区室可见强烈荧光。使用EGTA后,表面和内部荧光完全消失。综合电学和形态计量学数据计算细胞间连接的电阻。在正常条件下,连接膜的比电阻为0.4Ω·cm²,单个连接的电阻约为10¹¹Ω。使用EGTA时,相应的值增加约230%。连接电导降低的潜在机制尚不清楚。似乎与细胞质游离钙的升高无关。EGTA诱导的内阻增加表现为肌束长度常数的降低。讨论了“非典型缝隙连接”的性质及其与紧密连接的关系。得出的结论是,尽管颗粒的大小和排列不同,但在蛙心房肌中观察到的连接类似于昆虫或哺乳动物细胞的缝隙连接。提出了一个单间隙排列中肌束电行为的理论模型。(摘要截短于400字)