Editorial
Copyright ©2007 Baishideng Publishing Group Co.
World J Gastroenterol. Aug 14, 2007; 13(30): 4035-4041
Published online Aug 14, 2007. doi: 10.3748/wjg.v13.i30.4035
Figure 1
Figure 1 A: Human colonic myenteric plexus showing that neurons (white arrows) are less numerous with respect to EGC (black arrows) (NSE immunostaining, x 40); B: Semithin section of human colonic submucosal plexus, showing the preponderance of EGC (black arrows) with respect to the enteric neurons (white arrows) (Toluidine blue, x 40).
Figure 2
Figure 2 A: Full thickness section of the human colon, showing the submucosal (black arrow) and the myenteric plexus (white arrow) (HE, x10); B: Human myenteric ganglion, showing numerous EGC (black arrows) and an enteric neuron (white arrow) (HE, x 100).
Figure 3
Figure 3 EGC (arrows) tightly packed around enteric neurons in a submucosal (A) and a myenteric ganglion (B) (S100 immunostaining, x 40).
Figure 4
Figure 4 Electron microscopic image of glial cells (arrows) in a human colonic myenteric ganglion (x 1900).
Figure 5
Figure 5 Putative mechanisms linked to the decrease of enteric glial cells (EGC), leading to abnormal gut motility. EN: enteric neurons; ICC: interstitial cells of Cajal.