TTF-1 and HNF-3β in the developing tracheoesophageal fistula:: Further evidence for the respiratory origin of the 'distal esophagus'

被引:33
作者
Crisera, CA [1 ]
Connelly, PR [1 ]
Marmureanu, AR [1 ]
Lin, M [1 ]
Rose, MI [1 ]
Longaker, MT [1 ]
Gittes, GK [1 ]
机构
[1] NYU, Med Ctr, Dept Surg, Lab Dev Biol & Repair, New York, NY 10016 USA
关键词
tracheoesophageal fistula; organogenesis;
D O I
10.1016/S0022-3468(99)90003-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Purpose: Using an established rat model of esophageal atresia with tracheoesophageal fistula (EA-TEF), the authors have studied the organogenesis of this congenital anomaly. The authors previously have proposed that the "distal esophagus" actually is of respiratory lineage. In this report this hypothesis is tested by examining the expression of two foregut patterning transcription factors, thyroid transcription factor-1 (TTF-1) and hepatocyte nuclear factor-3 beta (HNF-3 beta), within the developing TEF. Methods: Pregnant Sprague-Dawley rats were injected with 2.2 mg/kg of Adriamycin intraperitoneally on days 6 to 9 of gestation. Using microdissection, the trachea, blind-ending esophagus, TEF, and stomach were isolated from embryos of various gestional ages. Immunohistochemistry was performed using polyclonal antibodies to TTF-1 and HNF-3 beta. Results: TTF-1 is a homeodomain protein that previously has been shown to be expressed in the lung and trachea but not in the gastrointestinal tract, and which, when deleted in a developing lung, results in a mouse with no peripheral lung parenchyma. TTF-1 was expressed strongly in the lung, fistula, and distal esophagus, but not in the proximal esophagus. HNF-3 beta is a forkhead transcription factor important in foregut patterning that binds and activates the TTF-1 promotor sequence. HNF-3 beta was expressed globally in the fistula and lung as well as the esophagus. Conclusions: The expression of the lung-specific transcription factor TTF-1 within the TEF strongly implies that the "distal esophagus" is a respiratory-derived structure and thus supports our theory of TEF organogenesis. The conservation of HNF-3 beta expression both in the TEF as well as the normal developing trachea and esophagus suggests that global foregut patterning is intact in the formation of this anomaly, and the defect lies at the lever of the respiratory Versus gastrointestinal commitment. J Pediatr Surg 34:1322-1326. Copyright (C) 1999 by W.B. Saunders Company.
引用
收藏
页码:1322 / 1326
页数:5
相关论文
共 20 条
  • [1] BERRY C, 1996, PAEDIAT PATHOLOGY, P207
  • [2] THE LUNG-SPECIFIC SURFACTANT PROTEIN-B GENE PROMOTER IS A TARGET FOR THYROID TRANSCRIPTION FACTOR-1 AND HEPATOCYTE NUCLEAR FACTOR-3, INDICATING COMMON FACTORS FOR ORGAN-SPECIFIC GENE-EXPRESSION ALONG THE FOREGUT AXIS
    BOHINSKI, RJ
    DILAURO, R
    WHITSETT, JA
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (09) : 5671 - 5681
  • [4] Esophageal atresia with tracheoesophageal fistula: Suggested mechanism in faulty organogenesis
    Crisera, CA
    Connelly, PR
    Marmureanu, AR
    Colen, KL
    Rose, MI
    Li, M
    Longaker, MT
    Gittes, GK
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1999, 34 (01) : 204 - 208
  • [5] Dahns B, 1992, PEDIAT PATHOLOGY, P653
  • [6] Hackett BP, 1996, ANNU REV PHYSIOL, V58, P51, DOI 10.1146/annurev.physiol.58.1.51
  • [7] HOLDER TM, 1993, PEDIAT SURG, P249
  • [8] Ikeda K, 1996, MOL CELL BIOL, V16, P3626
  • [9] LAZZARO D, 1991, DEVELOPMENT, V113, P1093
  • [10] Histopathologic study of esophageal atresia and tracheoesophageal fistula in an animal model
    Merei, J
    Kotsios, C
    Hutson, JM
    Hasthorpe, S
    [J]. JOURNAL OF PEDIATRIC SURGERY, 1997, 32 (01) : 12 - 14