Bekku S, Mochizuki H, Takayama E, Shinomiya N, Fukamachi H, Ichinose M, Tadakuma T, Yamamoto T
Department of Surgery I, National Defense Medical College, Saitama, Japan.
Res Exp Med (Berl). 1998 Dec;198(4):175-85. doi: 10.1007/s004330050101.
Carbonic anhydrase (CA) is an enzyme that is expressed in the intestine and catalyzes the reversible hydration of CO2 in the following reaction: CO2 + H2O<==>H2CO3<==>H(+)+HCO3-. To elucidate the association of CA expression with the differentiation of colonic enterocytes, we investigated the expression and localization of CA using a Northern blotting analysis, Western blotting analysis, and immunohistochemical staining. A Northern blotting analysis revealed an abundant expression of CA I and II mRNA in the colonic epithelial cells. However, the expression of CA III mRNA was not detected. According to the results of immunohistochemical staining of the human colonic mucosa using antisera against CA I and II, both CA I and II were localized on the cytoplasm of non-goblet columnar cells in the upper half of the crypts where more differentiated cells are located. According to the results of immunohistochemical staining of the rat colonic mucosa, neither CA I and II were detected at the new-born stage. The expression of CAs in the upper half of the crypts began to rise from 1 week after birth, and thereafter increased according to the growth of the rats. At 3 weeks after birth, the expression of CAs was almost the same as that of the adult rats. The amount of CA proteins evaluated by a Western blotting analysis revealed that the expression of CAs increased gradually until reaching a maximum level at 6 or 8 weeks. These results therefore suggest that CA I and II appear to be good markers for the differentiation of enterocytes in the colonic mucosa.
碳酸酐酶(CA)是一种在肠道中表达的酶,它催化二氧化碳的可逆水合反应:CO2 + H2O<==>H2CO3<==>H(+)+HCO3-。为了阐明CA表达与结肠肠上皮细胞分化的关系,我们使用Northern印迹分析、Western印迹分析和免疫组织化学染色来研究CA的表达和定位。Northern印迹分析显示结肠上皮细胞中CA I和II mRNA大量表达。然而,未检测到CA III mRNA的表达。根据使用抗CA I和II抗血清对人结肠黏膜进行免疫组织化学染色的结果,CA I和II均定位于隐窝上半部分非杯状柱状细胞的细胞质中,这些细胞所在位置的细胞分化程度更高。根据对大鼠结肠黏膜进行免疫组织化学染色的结果,在新生阶段未检测到CA I和II。隐窝上半部分CA的表达从出生后1周开始上升,此后随着大鼠的生长而增加。出生后3周,CA的表达与成年大鼠几乎相同。通过Western印迹分析评估的CA蛋白量显示,CA的表达逐渐增加,直至在6或8周时达到最高水平。因此,这些结果表明CA I和II似乎是结肠黏膜中肠上皮细胞分化的良好标志物。