Bush Toby G
Department of Physiology & Cell Biology and Department of Pharmacology, University of Nevada, School of Medicine, Anderson Medical Building, MS 352, Reno NV 89557-0046, USA.
Bioessays. 2002 Feb;24(2):130-40. doi: 10.1002/bies.10039.
As a direct consequence of the sophisticated arrangement of its intrinsic neurons, the gastrointestinal tract is unique among peripheral organs, in its ability to mediate its own reflexes. Neurons of the enteric nervous system are intimately associated with enteric glial cells. These supporting cells do not resemble Schwann cells, the glial cell found in all other parts of the peripheral nervous system, but share many similarities with astrocytes of the central nervous system. Ablation of enteric glial cells in adult transgenic mice has demonstrated that these cells are essential to maintain the integrity of the small intestine. Acute loss of enteric glial cells induces massive pathological changes with similarities to necrotizing enterocolitis (NEC) and early Crohn's disease. These human conditions share some mechanistic similarities. Identification of enteric glial cell dysfunction/loss as sufficient to induce necrotic/inflammatory bowel disease may be important to understand the pathogenesis of both NEC and Crohn's disease.
由于其内在神经元的精细排列,胃肠道在介导自身反射的能力方面,在外周器官中是独一无二的。肠神经系统的神经元与肠胶质细胞密切相关。这些支持细胞与施万细胞不同,施万细胞是外周神经系统所有其他部位发现的胶质细胞,但与中枢神经系统的星形胶质细胞有许多相似之处。成年转基因小鼠中肠胶质细胞的消融表明,这些细胞对于维持小肠的完整性至关重要。肠胶质细胞的急性丧失会引发大量病理变化,与坏死性小肠结肠炎(NEC)和早期克罗恩病相似。这些人类病症在一些机制上有相似之处。确定肠胶质细胞功能障碍/丧失足以诱发坏死性/炎症性肠病,对于理解NEC和克罗恩病的发病机制可能很重要。