CDX2
医学
溃疡性结肠炎
同源盒
活检
杯状细胞
内科学
病理
免疫学
胃肠病学
癌症研究
转录因子
上皮
疾病
生物
基因
生物化学
作者
Kiichiro Tsuchiya,Ryohei Hayashi,K Fukushima,Shuji Hibiya,Nobukatsu Horita,Mariko Negi,Eisaku Itoh,Takumi Akashi,Yoshinobu Eishi,Satoshi Motoya,Yoshiaki Takeuchi,Reiko Kunisaki,Ken Fukunaga,Shirô Nakamura,Naoki Yoshimura,Masakazu Takazoe,Bunei Iizuka,Yasuo Suzuki,Masakazu Nagahori,Mamoru Watanabe
摘要
Ulcerative colitis (UC) is a chronic inflammatory disease of the colon with an intractable, recurrent course. Although the goal of UC therapy has recently been to target mucosal healing, the molecular mechanism of mucosal healing remains unknown. In this study, we aimed to elucidate the molecular dynamics related to the proliferation and differentiation of intestinal epithelial cells during cytapheresis therapy in a short duration.Endoscopy was performed in 26 patients with UC in multicentre hospitals, and biopsy specimens were collected from the rectum before and within two weeks after leukocytapheresis (LCAP). The expression of representative proteins in intestinal epithelial cells and pathological findings was compared before and after LCAP.The expression of caudal type homeobox 2 (CDX2) and a hes family bHLH transcription factor 1(HES1) markedly increased after LCAP. Patients with endoscopic improvement after LCAP showed the expression of CDX2 before LCAP. Moreover, the number of goblet cells significantly increased after LCAP. Patients without endoscopic improvement after LCAP did not show the expression of CDX2 before LCAP. However, the expression of CDX2 markedly increased after LCAP.This study suggests that cytapheresis might induce CDX2 expression without affecting the cell proliferation, thus resulting in mucosal healing with goblet cell restoration.
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