Bódi Nikolett, Mezei Diána, Chakraborty Payal, Szalai Zita, Barta Bence Pál, Balázs János, Rázga Zsolt, Hermesz Edit, Bagyánszki Mária
Department of Physiology, Anatomy and Neuroscience, Faculty of Science and Informatics, University of Szeged, Szeged 6726, Hungary.
Department of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Szeged 6726, Hungary.
World J Diabetes. 2021 May 15;12(5):658-672. doi: 10.4239/wjd.v12.i5.658.
The importance of the neuronal microenvironment has been recently highlighted in gut region-specific diabetic enteric neuropathy. Regionally distinct thickening of endothelial basement membrane (BM) of intestinal capillaries supplying the myenteric ganglia coincide with neuronal damage in different intestinal segments. Accelerated synthesis of matrix molecules and reduced degradation of matrix components may also contribute to the imbalance of extracellular matrix dynamics resulting in BM thickening. Among the matrix degrading proteinases, matrix metalloproteinase 9 (MMP9) and its tissue inhibitor (TIMP1) are essential in regulating extracellular matrix remodelling.
To evaluate the intestinal segment-specific effects of diabetes and insulin replacement on ganglionic BM thickness, MMP9 and TIMP1 expression.
Ten weeks after the onset of hyperglycaemia gut segments were taken from the duodenum and ileum of streptozotocin-induced diabetic, insulin-treated diabetic and sex- and age-matched control rats. The thickness of BM surrounding myenteric ganglia was measured by electron microscopic morphometry. Whole-mount preparations of myenteric plexus were prepared from the different gut regions for MMP9/TIMP1 double-labelling fluorescent immunohistochemistry. Post-embedding immunogold electron microscopy was applied on ultrathin sections to evaluate the MMP9 and TIMP1 expression in myenteric ganglia and their microenvironment from different gut segments and conditions. The MMP9 and TIMP1 messenger ribonucleic acid (mRNA) level was measured by quantitative polymerase chain reaction.
Ten weeks after the onset of hyperglycaemia, the ganglionic BM was significantly thickened in the diabetic ileum, while it remained intact in the duodenum. The immediate insulin treatment prevented the diabetes-related thickening of the BM surrounding the ileal myenteric ganglia. Quantification of particle density showed an increasing tendency for MMP9 and a decreasing tendency for TIMP1 from the proximal to the distal small intestine under control conditions. In the diabetic ileum, the number of MMP9-indicating gold particles decreased in myenteric ganglia, endothelial cells of capillaries and intestinal smooth muscle cells, however, it remained unchanged in all duodenal compartments. The MMP9/TIMP1 ratio was also decreased in ileal ganglia only. However, a marked segment-specific induction was revealed in MMP9 and TIMP1 at the mRNA levels.
These findings support that the regional decrease in MMP9 expression in myenteric ganglia and their microenvironment may contribute to extracellular matrix accumulation, resulting in a region-specific thickening of ganglionic BM.
神经元微环境的重要性最近在肠道区域特异性糖尿病性肠神经病变中得到了强调。供应肌间神经节的肠毛细血管内皮基底膜(BM)区域特异性增厚与不同肠段的神经元损伤相一致。基质分子合成加速和基质成分降解减少也可能导致细胞外基质动态失衡,从而导致BM增厚。在基质降解蛋白酶中,基质金属蛋白酶9(MMP9)及其组织抑制剂(TIMP1)在调节细胞外基质重塑中至关重要。
评估糖尿病和胰岛素替代对神经节BM厚度、MMP9和TIMP1表达的肠段特异性影响。
高血糖发作10周后,从链脲佐菌素诱导的糖尿病大鼠、胰岛素治疗的糖尿病大鼠以及性别和年龄匹配的对照大鼠的十二指肠和回肠中取出肠段。通过电子显微镜形态计量学测量肌间神经节周围BM的厚度。从不同肠道区域制备肌间神经丛整装标本,用于MMP9/TIMP1双标记荧光免疫组织化学。对超薄切片应用包埋后免疫金电子显微镜,以评估不同肠道段和条件下肌间神经节及其微环境中MMP9和TIMP1的表达。通过定量聚合酶链反应测量MMP9和TIMP1信使核糖核酸(mRNA)水平。
高血糖发作10周后,糖尿病回肠中的神经节BM显著增厚,而十二指肠中的BM保持完整。立即进行胰岛素治疗可防止糖尿病相关的回肠肌间神经节周围BM增厚。颗粒密度定量显示,在对照条件下,从近端小肠到远端小肠,MMP9有增加趋势,TIMP1有减少趋势。在糖尿病回肠中,肌间神经节、毛细血管内皮细胞和肠平滑肌细胞中指示MMP9的金颗粒数量减少,但在所有十二指肠区室中保持不变。仅回肠神经节中的MMP9/TIMP1比值也降低。然而,在mRNA水平上,MMP9和TIMP1有明显的段特异性诱导。
这些发现支持肌间神经节及其微环境中MMP9表达的区域减少可能导致细胞外基质积累,从而导致神经节BM区域特异性增厚。