PMID- 20385283 OWN - NLM STAT- MEDLINE DCOM- 20100714 LR - 20191210 IS - 1531-5037 (Electronic) IS - 0022-3468 (Linking) VI - 45 IP - 4 DP - 2010 Apr TI - Hoxd-13 expression in the development of hindgut in ethylenethiourea-exposed fetal rats. PG - 755-61 LID - 10.1016/j.jpedsurg.2009.11.011 [doi] AB - PURPOSE: Hoxd-13, as one of the most posterior genes among Hox genes, was reported to play a critical role in the development of the most posterior alimentary canal in vertebrates. This study investigated the expression pattern of Hoxd-13 in the hindgut development of the normal and ethylenethiourea (ETU)-exposed rat embryos with anorectal malformations (ARMs) to find out the possible role of Hoxd-13 in the hindgut development and anorectal morphogenesis. MATERIAL AND METHOD: The ETU murine model of ARMs was used via ETU 1% (125 mg/kg) on gestational day (gD) 10. Embryos were harvested via cesarean delivery on gD13 to gD21. Temporal and spatial expression of Hoxd-13 was evaluated in the normal fetal rats (n = 215) and ARMs rats (n = 218) using immunohistochemistry staining, reverse transcriptase polymerase chain reaction, and Western blot analysis. RESULTS: Immunohistochemistry staining revealed that Hoxd-13 expression was confined to the epithelium of the hindgut, cloacal membrane, and urogenital sinus as well as the mesenchyme of the urorectal septum at all gestations in the normal group; however, in the ARMs group, the signal specific for Hoxd-13 was weak in the epithelium of the hindgut and cloacal membrane as well as the mesenchyme of the urorectal septum. Western blot analysis and reverse transcriptase polymerase chain reaction revealed that the level of Hoxd-13 expression was significantly decreased in the ARMs embryos compared with that in the normal embryos on gD13 to gD16 (P < .05) rather than on gD18 to gD21. CONCLUSIONS: The aberrations in spatiotemporal expression pattern of Hoxd-13 on gD13 to gD16 suggested that Hoxd-13 may be an essential inductive signal for normal development of the hindgut, and altered expression may contribute to the abnormal development of the hindgut and accordingly lead to ARMs. CI - Copyright 2010 Elsevier Inc. All rights reserved. FAU - Dan, Zhang AU - Dan Z AD - Department of Pediatric Surgery, The Second Affiliated Hospital, China Medical University, Shenyang 110004, PR China. FAU - Bo, Zhang Zhi AU - Bo ZZ FAU - Tao, Zhang AU - Tao Z FAU - Wei, Zhang Shi AU - Wei ZS FAU - Jia, Wang Da AU - Jia WD FAU - Cheng, Zhang Shu AU - Cheng ZS FAU - Wei, Yuan Zheng AU - Wei YZ FAU - Wang, Wei-Lin AU - Wang WL LA - eng PT - Evaluation Study PT - Journal Article PL - United States TA - J Pediatr Surg JT - Journal of pediatric surgery JID - 0052631 RN - 0 (Homeodomain Proteins) RN - 0 (Transcription Factors) RN - 24FOJ4N18S (Ethylenethiourea) SB - IM MH - Anal Canal/*abnormalities/embryology MH - Animals MH - Blotting, Western MH - Digestive System Abnormalities/*embryology/genetics/metabolism MH - Ethylenethiourea MH - Female MH - Homeodomain Proteins/genetics/*metabolism MH - Immunohistochemistry MH - Male MH - Rats MH - Rats, Wistar MH - Rectum/*abnormalities/embryology MH - Reverse Transcriptase Polymerase Chain Reaction MH - Transcription Factors/genetics/*metabolism EDAT- 2010/04/14 06:00 MHDA- 2010/07/16 06:00 CRDT- 2010/04/14 06:00 PHST- 2009/05/07 00:00 [received] PHST- 2009/11/12 00:00 [revised] PHST- 2010/11/12 00:00 [accepted] PHST- 2010/04/14 06:00 [entrez] PHST- 2010/04/14 06:00 [pubmed] PHST- 2010/07/16 06:00 [medline] AID - S0022-3468(09)00942-7 [pii] AID - 10.1016/j.jpedsurg.2009.11.011 [doi] PST - ppublish SO - J Pediatr Surg. 2010 Apr;45(4):755-61. doi: 10.1016/j.jpedsurg.2009.11.011.