Tissue-Engineered Small Intestine and Stomach Form from Autologous Tissue in a Preclinical Large Animal Model

Journal of Surgical Research

Volumn 156, Issue 2, 2009, Pages 205-212

  Sala, Frédéric G ^a   Kunisaki, Shaun M ^b   Ochoa, Erin R ^b   Vacanti, Joseph ^b   Grikscheit, Tracy C ^a  

^a CHILDREN S HOSPITAL LOS ANGELES   (United States)

^b MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

intestinal stem cell niche; preclinical large animal model; short bowel syndrome; small intestine; tissue engineering

Indexed keywords

DCAMKL 1 PROTEIN; PROTEIN KINASE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; AUTOGRAFT; COLUMNAR EPITHELIUM; CONTROLLED STUDY; HISTOLOGY; IMMUNOHISTOCHEMISTRY; INTESTINE GRAFT; JEJUNUM; MALE; NONHUMAN; PIGLET; PRIORITY JOURNAL; STOMACH; STOMACH ANTRUM; SWINE; TISSUE ENGINEERING;

ANIMALS; IMMUNOHISTOCHEMISTRY; JEJUNUM; MALE; MODELS, ANIMAL; ORGANOIDS; REGENERATION; STEM CELLS; STOMACH; SWINE; TISSUE ENGINEERING; TISSUE SCAFFOLDS; TRANSPLANTATION, AUTOLOGOUS;

EID: 70249144629     PISSN: 00224804     EISSN: 10958673     Source Type: Journal    
DOI: 10.1016/j.jss.2009.03.062     Document Type: Article

References (44)

1. Sankaran K., Puckett B., Lee D.S., et al. Variations in incidence of necrotizing enterocolitis in Canadian neonatal intensive care units. J Pediatr Gastroenterol Nutr 39 (2004) 366
2. Ballance W.A., Dahms B.B., Shenker N., et al. Pathology of neonatal necrotizing enterocolitis: A 10-year experience. J Pediatr 117 (1990) S6
3. Bell M.J., Ternberg J.L., Feigin R.D., et al. Neonatal necrotizing enterocolitis. Therapeutic decisions based upon clinical staging. Ann Surg 187 (1978) 1
4. Callaghan W.M., MacDorman M.F., Rasmussen S.A., et al. The contribution of preterm birth to infant mortality rates in the United States. Pediatrics 118 (2006) 1566
5. Cassady G., Crouse D.T., Kirklin J.W., et al. A randomized, controlled trial of very early prophylactic ligation of the ductus arteriosus in babies who weighed 1000 g or less at birth. N Engl J Med 320 (1989) 1511
6. Cikrit D., Mastandrea J., West K.W., et al. Necrotizing enterocolitis: Factors affecting mortality in 101 surgical cases. Surgery 96 (1984) 648
7. Collins S.R., Griffin M.R., Arbogast P.G., et al. The rising prevalence of gastroschisis and omphalocele in Tennessee. J Pediatr Surg 42 (2007) 1221
8. Kim H.B., Fauza D., Garza J., et al. Serial transverse enteroplasty (STEP): A novel bowel lengthening procedure. J Pediatr Surg 38 (2003) 425
9. Kliegman R.M. Models of the pathogenesis of necrotizing enterocolitis. J Pediatr 117 (1990) S2
10. Kliegman R.M., and Fanaroff A.A. Necrotizing enterocolitis. N Engl J Med 310 (1984) 1093
11. Kosloske A.M. Operative techniques for the treatment of neonatal necrotizing enterocolitis. Surg Gynecol Obstetrics 149 (1979) 740
12. Kosloske A.M. Indications for operation in necrotizing enterocolitis revisited. J Pediatr Surg 29 (1994) 663
13. Kosloske A.M., and Lilly J.R. Paracentesis and lavage for diagnosis of intestinal gangrene in neonatal necrotizing enterocolitis. J Pediatr Surg 13 (1978) 315
14. Limmer J., Gortner L., Kelsch G., et al. Diagnosis and treatment of necrotizing enterocolitis. A retrospective evaluation of abdominal paracentesis and continuous postoperative lavage. Acta Paediatr 396 Suppl (1994) 65
15. Luig M., and Lui K. Epidemiology of necrotizing enterocolitis-Part I: Changing regional trends in extremely preterm infants over 14 years. J Paediatr Child Health 41 (2005) 169
16. Lynch L., O'Donoghue D., Dean J., et al. Detection and characterization of hemopoietic stem cells in the adult human small intestine. J Immunol 176 (2006) 5199
17. Mallick I.H., Yang W., Winslet M.C., et al. Ischemia-reperfusion injury of the intestine and protective strategies against injury. Dig Dis Sci 49 (2004) 1359
18. Martinez-Tallo E., Claure N., and Bancalari E. Necrotizing enterocolitis in full-term or near-term infants: Risk factors. Biol Neonate 71 (1997) 292
19. Moss R.L., Das J.B., and Raffensperger J.G. Necrotizing enterocolitis and total parenteral nutrition-associated cholestasis. Nutrition 12 (1996) 340
20. O'Donovan D.J., Baetiong A., Adams K., et al. Necrotizing enterocolitis and gastrointestinal complications after indomethacin therapy and surgical ligation in premature infants with patent ductus arteriosus. J Perinatol 23 (2003) 286
21. Reyes J., Bueno J., Kocoshis S., et al. Current status of intestinal transplantation in children. J Pediatr Surg 33 (1998) 243
22. Grant D., Abu-Elmagd K., Reyes J., et al. 2003 report of the intestine transplant registry: A new era has dawned. Ann Surg 241 (2005) 607
23. Choi R.S., and Vacanti J.P. Preliminary studies of tissue-engineered intestine using isolated epithelial organoid units on tubular synthetic biodegradable scaffolds. Transplant Proc 29 (1997) 848
24. Grikscheit T., Ochoa E.R., Srinivasan A., et al. Tissue-engineered esophagus: Experimental substitution by onlay patch or interposition. J Thorac Cardiovasc Surg 126 (2003) 537
25. Grikscheit T., Srinivasan A., and Vacanti J.P. Tissue-engineered stomach: A preliminary report of a versatile in vivo model with therapeutic potential. J Pediatr Surg 38 (2003) 1305
26. Grikscheit T.C., Ochoa E.R., Ramsanahie A., et al. Tissue-engineered large intestine resembles native colon with appropriate in vitro physiology and architecture. Ann Surg 238 (2003) 35
27. Grikscheit T.C., Ogilvie J.B., Ochoa E.R., et al. Tissue-engineered colon exhibits function in vivo. Surgery 132 (2002) 200
28. Grikscheit T.C., Siddique A., Ochoa E.R., et al. Tissue-engineered small intestine improves recovery after massive small bowel resection. Ann Surg 240 (2004) 748
29. Grikscheit T.C., and Vacanti J.P. The history and current status of tissue engineering: The future of pediatric surgery. J Pediatr Surg 37 (2002) 277
30. Evans G.S., Flint N., Somers A.S., et al. The development of a method for the preparation of rat intestinal epithelial cell primary cultures. J Cell Sci 101 Pt 1 (1992) 219
31. Andoh A., Bamba S., Brittan M., et al. Role of intestinal subepithelial myofibroblasts in inflammation and regenerative response in the gut. Pharmacol Ther 114 (2007) 94
32. Ramalho-Santos M., Melton D.A., and McMahon A.P. Hedgehog signals regulate multiple aspects of gastrointestinal development. Development 127 (2000) 2763
33. Sancho E., Batlle E., and Clevers H. Signaling pathways in intestinal development and cancer. Annu Rev Cell Dev Biol 20 (2004) 695
34. Gregorieff A., Pinto D., Begthel H., et al. Expression pattern of Wnt signaling components in the adult intestine. Gastroenterology 129 (2005) 626
35. Kaestner K.H., Silberg D.G., Traber P.G., et al. The mesenchymal winged helix transcription factor Fkh6 is required for the control of gastrointestinal proliferation and differentiation. Genes Dev 11 (1997) 1583
36. Korinek V., Barker N., Moerer P., et al. Depletion of epithelial stem-cell compartments in the small intestine of mice lacking Tcf-4. Nat Genet 19 (1998) 379
37. Louvard D., Kedinger M., and Hauri H.P. The differentiating intestinal epithelial cell: Establishment and maintenance of functions through interactions between cellular structures. Annu Rev Cell Biol 8 (1992) 157
38. May R., Riehl T.E., Hunt C., et al. Identification of a novel putative gastrointestinal stem cell and adenoma stem cell marker, double cortin and CaM kinase-like-1, following radiation injury and in adenomatous polyposis coli/multiple intestinal neoplasia mice. Stem Cells 26 (2008) 630
39. Potten C.S., Booth C., and Pritchard D.M. The intestinal epithelial stem cell: The mucosal governor. Int J Exp Pathol 78 (1997) 219
40. Powell D.W., Mifflin R.C., Valentich J.D., et al. Myofibroblasts. II. Intestinal subepithelial myofibroblasts. Am J Physiol 277 (1999) C183
41. Madison B.B., Braunstein K., Kuizon E., et al. Epithelial hedgehog signals pattern the intestinal crypt-villus axis. Development 132 (2005) 279
42. Simon-Assmann P., and Kedinger M. Heterotypic cellular cooperation in gut morphogenesis and differentiation. Semin Cell Biol 4 (1993) 221
43. Li X., Madison B.B., Zacharias W., et al. Deconvoluting the intestine: Molecular evidence for a major role of the mesenchyme in the modulation of signaling cross talk. Physiol Genomics 29 (2007) 290
44. Ormestad M., Astorga J., Landgren H., et al. Foxf1 and Foxf2 control murine gut development by limiting mesenchymal Wnt signaling and promoting extracellular matrix production. Development 133 (2006) 833