Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Amyloid. 2013 Jun;20(2):99-106. doi: 10.3109/13506129.2013.787985. Epub 2013 May 3.
Hereditary transthyretin (TTR) amyloidosis is a systemic neuropathic disorder caused by TTR gene mutations. Gastrointestinal complications are common and the underlying mechanisms remain unclear. The interstitial cells of Cajal (ICC) function as pacemaker cells in the gastrointestinal tract and are important for gastrointestinal motility. The aim of this study was to investigate the densities of gastric ICC and nerves in patients with TTR amyloidosis compared to non-amyloidosis controls.
Antral wall autopsy specimens from 11 Japanese ATTR V30M patients and 10 controls were analyzed with immunohistochemistry and computerized analysis. Antibodies to c-Kit and TMEM16A were used to assess ICC and an antibody to PGP 9.5 was used to assess nervous tissue. The study was approved by a Japanese ethical committee.
The densities of c-Kit-immunoreactive (IR) ICC were significantly lower in the circular and longitudinal muscle layers of patients compared to controls (p = 0.004 for both). Equivalent results were found for TMEM16A-IR ICC. There were no significant differences in PGP 9.5-IR cells in the circular or longitudinal muscle layers between patients and controls (p = 0.173 and 0.099, respectively).
A loss of gastrointestinal ICC may be an important factor for the digestive disturbances in hereditary TTR amyloidosis.
遗传性转甲状腺素蛋白(TTR)淀粉样变性是一种由 TTR 基因突变引起的系统性神经病变。胃肠道并发症很常见,但潜在机制尚不清楚。Cajal 间质细胞(ICC)作为胃肠道的起搏细胞,对胃肠道动力很重要。本研究旨在比较 TTR 淀粉样变性患者和非淀粉样变性对照组胃 ICC 和神经的密度。
对 11 例日本 ATTR V30M 患者和 10 例对照者的胃窦壁尸检标本进行免疫组织化学和计算机分析。使用 c-Kit 和 TMEM16A 抗体评估 ICC,使用 PGP 9.5 抗体评估神经组织。该研究得到了日本伦理委员会的批准。
与对照组相比,患者的环形和纵行肌层中 c-Kit 免疫反应性(IR)ICC 的密度显著降低(p = 0.004)。TMEM16A-IR ICC 也有类似的结果。患者和对照组的环形或纵行肌层中 PGP 9.5-IR 细胞无显著差异(p = 0.173 和 0.099)。
胃肠道 ICC 的丧失可能是遗传性 TTR 淀粉样变性消化功能紊乱的一个重要因素。