Kirk K L, Bell P D, Barfuss D W, Ribadeneira M
Am J Physiol. 1985 Jun;248(6 Pt 2):F890-4. doi: 10.1152/ajprenal.1985.248.6.F890.
Direct examination of the structure and function of the macula densa is compromised by the relative inaccessibility and small size of this cell plaque. We report the isolation and perfusion of rabbit nephron segments with attached glomeruli and the direct visualization of the macula densa with differential interference-contrast microscopy. We used this technique to examine the structural sensitivity of the macula densa to perturbations in luminal osmolality and NaCl concentration. Reducing luminal osmolality from 290 to 70 mosmol/kg by removing NaCl resulted in a dilation of the lateral intercellular spaces that was both reversible and specific to the region of the macula densa. Associated with the dilation of the intercellular spaces was a small (congruent to 10%), but statistically significant, increase in the height of the macula densa cells. These structural events were related to the reduction in luminal osmolality, since isosmotic replacement of NaCl with mannitol resulted in no detectable structural changes. Thus, the macula densa may represent a small water-permeable plaque of cells within the remaining water-impermeable thick ascending limb of Henle's loop.
致密斑的结构和功能的直接检查受到该细胞斑相对难以接近和尺寸较小的影响。我们报告了对带有附着肾小球的兔肾单位节段进行分离和灌注,并使用微分干涉相差显微镜直接观察致密斑。我们使用该技术来检查致密斑对管腔渗透压和氯化钠浓度扰动的结构敏感性。通过去除氯化钠将管腔渗透压从290降低到70 mosmol/kg,导致细胞间外侧间隙扩张,这种扩张是可逆的且特异于致密斑区域。与细胞间间隙扩张相关的是致密斑细胞高度有小幅(约10%)但具有统计学意义的增加。这些结构变化与管腔渗透压降低有关,因为用甘露醇等渗替代氯化钠未导致可检测到的结构变化。因此,致密斑可能代表亨氏袢其余不透水的厚升支内一小片可透水的细胞斑。