Pathophysiology in microvillus inclusion disease

Zeitschrift fur Gastroenterologie

Volumn 44, Issue 8, 2006, Pages 667-671

  Reinshagen, Konrad ^a   Naim, H ^b   Heusipp, G ^c   Zimmer, K P ^c  

^a UNIVERSITY OF HEIDELBERG   (Germany)

^b UNIVERSITY OF VETERINARY MEDICINE HANNOVER   (Germany)

^c UNIVERSITY HOSPITAL MÜNSTER   (Germany)

Author keywords

Hereditary diarrhea; Microvillus inclusion bodies; Pediatric gastroenterology

Indexed keywords

CYTOPLASM; DIARRHEA; ELECTRON MICROSCOPY; GASTROINTESTINAL DISEASE; HUMAN; INTESTINE BRUSH BORDER; INTESTINE BYPASS; INTESTINE CELL; INTESTINE EPITHELIUM CELL; MICROVILLUS INCLUSION DISEASE; PERIODIC ACID SCHIFF STAIN; REVIEW;

DIARRHEA; HUMANS; INCLUSION BODIES; MALABSORPTION SYNDROMES; MICROVILLI;

EID: 33748670921     PISSN: 00442771     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2006-926903     Document Type: Review

References (31)

1. Murch SH. Toward a molecular understanding of complex childhood enteropathies. J Pediatr Gastroenterol Nutr 2002; 34: 4-10
2. Davidson G, Cutz E, Hamilton J et al. Familial enteropathy: A syndrome of protracted diarrhea from birth, failure to thrive, and hypoplastic villous atrophy. Gastroenterology 1978; 75: 783-790
3. Phillips A, Schmilz J. Familial microvillus atrophy: A clinico-pathological survey of 23 cases. J Pediatr Gastroenterol Nutr 1992; 14: 380-396
4. Rhoads JM, Vogler RC, Lacey SR et al. Microvillus inclusion disease: in vitro jejunal electrolyte transport. Gastroenterology 1991; 100: 811-817
5. Cutz E, Rhoads M, Drumm B et al. Microvillus inclusion disease: An inherited defect of brush-border assembly and differentiation. N Engl J Med 1989; 320: 646-651
6. Pohl JF, Shub MD, Trevelline EE et al. A cluster of microvillous inclusion disease in the Navajo population. J Pediatr 1999; 134: 103-106
7. Nathavitharana KA, Green NJ, Raafat F et al. Siblings with microvillous inclusion disease. Arch Dis Child 1994; 71: 71-73
8. Cutz E, Sherman PM, Davidson GP. Enteropathies associated with protracted diarrhea of infancy: clinicopathological features, cellular and molecular mechanisms. Pediatr Pathol Lab Med 1997; 17: 335-368
9. Phillips A, Jenkins P, Raafat F et al. Congenital microvillus atrophy: Specific diagnostic features. Arch Dis Child 1985; 60: 135-140
10. Groisman GM, Amar M, Livne E. CDlO: a valuable tool for the light microscopic diagnosis of microvillous inclusion disease (familial microvillous atrophy). Am J Surg Pathol 2002; 26: 902-907
11. Groisman GM, Ben-Izhak O, Schwersenz A et al. The value of polyclonal carcinoembryonic antigen immunostaining in the diagnosis of microvillous inclusion disease. Hum Pathol 1993; 24: 1232-1237
12. Groisman GM, Sabo E, Meir A et al. Enterocyte apoptosis and proliferation are increased in microvillous inclusion disease (familial microvillous atrophy). Hum Pathol 2000; 31: 1404-1410
13. Bell SW, Kerner Jr JA, Sibley RK. Microvillous inclusion disease. The importance of electron microscopy for diagnosis. Am J Surg Pathol 1991; 15: 1157-1164
14. Phillips A, Szafransky M, Man LY et al. Periodic Acid-Schiff staining abnormality in microvillus atrophy: Photometric and ultrastructural studies. J Pediatr Gastroenterol Nutr 2000; 30: 34-42
15. Ameen NA, Salas P. Microvillus inclusion disease: A genetic defect affecting apical membrane protein traffic in intestinal epithelium. Traffic 2000; 1: 76-83
16. Phillips A, Fransen J, Hauri HP et al. The constitutive pathway in microvillus atrophy. J Pediatr Gastroenterol Nutr 1993; 17: 239-246
17. Reinshagen K, Nairn HY, Zimmer KP. Autophagocytosis of the apical membrane in microvillus inclusion disease. Gut 2002; 51: 514-521
18. Phillips AD, Brown A, Hicks S et al. Acetylated sialic acid residues and blood group antigens localise within the epithelium in microvillous atrophy indicating internal accumulation of the glycocalyx. Gut 2004; 53: 1764-1771
19. Apodaca G. Endocytic traffic in polarized epithelial cells: role of the actin and microtubule cytoskeleton. Traffic 2001; 2: 149-159
20. Valentijn K, Valentijn JA, Jamieson JD. Role of actin in regulated exocytosis and compensatory membrane retrieval: insights from an old acquaintance. Biochem Biophys Res Commun 1999; 266: 652-661
21. Hamm-Alvarez SF, Sheetz MP. Microtubule-dependent vesicle transport: modulation of channel and transporter activity in liver and kidney Physiol Rev 1998; 78: 1109-1129
22. Drumm B, Cutz E, Tomkins KB et al. Urogastrone/epidermal growth factor in treatment of congenital microvillous atrophy. Lancet 1988; 16: 111-112
23. Couper RT, Berzen A, Berall G et al. Clinical response to the long acting somatostatin analogue SMS 201-995 in a child with congenital microvillus atrophy. Gut 1989; 30: 1020-1024
24. Croft NM, Howatson AG, Ling SC et al. Microvillous inclusion disease: an evolving condition. J Pediatr Gastroenterol Nutr 2000; 31: 185-189
25. Colomb V, Goulet O, Ricour C. Home enteral and parenteral nutrition in children. Baillieres Clin Gastroenterol 1998; 12: 877-894
26. Ruemmele FM, Jan D, Lacaille F et al. New perspectives for children with microvillous inclusion disease: early small bowel transplantation. Transplantation 2004; 77: 1024-1028
27. Nelson WJ. Adaptation of core mechanisms to generate cell polarity. Nature 2003; 17: 766-774
28. Segal G, Lee W, Arora PD et al. Involvement of actin filaments and integrins in the binding step in collagen phagocytosis by human fibroblasts. J Cell Sci 2001; 114: 119-129
29. Holen I, Stromhaug PE, Gordon PB et al. Inhibition of autophagy and multiple steps in asialoglycoprotein endocytosis by inhibitors of tyrosine protein kinases (tyrphostins). J Biol Chem 1995; 270: 12823-12831
30. Barbieri JT, Sun J. Pseudomonas aeruginosa ExoS and ExoT. Rev Physiol Biochem Pharmacol 2004; 152: 79-92
31. Viboud GI, Bliska JB. Yersinia outer proteins: role in modulation of host cell signalling responses and pathogenesis. Annu Rev Microbiol 2005; 59: 69-89