Haveri Hanna, Westerholm-Ormio Mia, Lindfors Katri, Mäki Markku, Savilahti Erkki, Andersson Leif C, Heikinheimo Markku
Children's Hospital, University of Helsinki, Helsinki, Finland.
BMC Gastroenterol. 2008 Apr 11;8:9. doi: 10.1186/1471-230X-8-9.
Human gastrointestinal mucosa regenerates vigorously throughout life, but the factors controlling cell fate in mature mucosa are poorly understood. GATA transcription factors direct cell proliferation and differentiation in many organs, and are implicated in tumorigenesis. GATA-4 and GATA-6 are considered crucial for the formation of murine gastrointestinal mucosa, but their role in human gastrointestinal tract remains unexplored. We studied in detail the expression patterns of these two GATA factors and a GATA-6 down-stream target, Indian hedgehog (Ihh), in normal human gastrointestinal mucosa. Since these factors are considered important for proliferation and differentiation, we also explored the possible alterations in their expression in gastrointestinal neoplasias. The expression of the carcinogenesis-related protein Indian hedgehog was also investigated in comparison to GATA factors.
Samples of normal and neoplastic gastrointestinal tract from children and adults were subjected to RNA in situ hybridization with 33P labelled probes and immunohistochemistry, using an avidin-biotin immunoperoxidase system. The pathological tissues examined included samples of chronic and atrophic gastritis as well as adenomas and adenocarcinomas of the colon and rectum.
GATA-4 was abundant in the differentiated epithelial cells of the proximal parts of the gastrointestinal tract but was absent from the distal parts. In contrast, GATA-6 was expressed throughout the gastrointestinal epithelium, and in the distal gut its expression was most intense at the bottom of the crypts, i.e. cells with proliferative capacity. Both factors were also present in Barrett's esophagus and metaplasia of the stomach. GATA-6 expression was reduced in colon carcinoma. Ihh expression overlapped with that of GATA-6 especially in benign gastrointestinal neoplasias.
The results suggest differential but overlapping functions for GATA-4 and GATA-6 in the normal gastrointestinal mucosa. Furthermore, GATA-4, GATA-6 and Ihh expression is altered in premalignant dysplastic lesions and reduced in overt cancer.
人类胃肠道黏膜在一生中都能旺盛地再生,但成熟黏膜中控制细胞命运的因素却知之甚少。GATA转录因子在许多器官中指导细胞增殖和分化,并与肿瘤发生有关。GATA - 4和GATA - 6被认为对小鼠胃肠道黏膜的形成至关重要,但其在人类胃肠道中的作用仍未得到探索。我们详细研究了这两种GATA因子以及一种GATA - 6下游靶点印度刺猬因子(Ihh)在正常人类胃肠道黏膜中的表达模式。由于这些因子被认为对增殖和分化很重要,我们还探讨了它们在胃肠道肿瘤中表达的可能变化。与GATA因子相比,还研究了致癌相关蛋白印度刺猬因子的表达。
使用33P标记的探针和抗生物素蛋白 - 生物素免疫过氧化物酶系统,对儿童和成人的正常及肿瘤性胃肠道样本进行RNA原位杂交和免疫组织化学检测。检查的病理组织包括慢性萎缩性胃炎样本以及结肠和直肠的腺瘤和腺癌。
GATA - 4在胃肠道近端的分化上皮细胞中丰富,但在远端部分不存在。相反,GATA - 6在整个胃肠道上皮中表达,在远端肠道中,其表达在隐窝底部最为强烈,即具有增殖能力的细胞。这两种因子也存在于巴雷特食管和胃化生中。GATA - 6在结肠癌中的表达降低。Ihh的表达与GATA - 6的表达重叠,尤其是在良性胃肠道肿瘤中。
结果表明GATA - 4和GATA - 6在正常胃肠道黏膜中具有不同但重叠的功能。此外,GATA - 4、GATA - 6和Ihh的表达在癌前发育异常病变中发生改变,在明显的癌症中降低。