Ang H L, Deltour L, Zgombić-Knight M, Wagner M A, Duester G
Burnham Institute, La Jolla, California 92037, USA.
Alcohol Clin Exp Res. 1996 Sep;20(6):1050-64. doi: 10.1111/j.1530-0277.1996.tb01946.x.
Vitamin A (retinol) regulates embryonic development and adult epithelial function via metabolism to retinoic acid, a pleiotrophic regulator of gene expression. Retinoic acid is synthesized locally and functions in an autocrine or paracrine fashion, but the enzymes involved remain obscure. Alcohol dehydrogenase (ADH) isozymes capable of metabolizing retinol include class I and class IV ADHs, with class III ADH unable to perform this function. ADHs also metabolize ethanol, and high levels of ethanol inhibit retinol metabolism, suggesting a possible mode of action for some of the medical complications of alcoholism. To explore whether any ADH isozymes are linked to retinoic acid synthesis, herein we have examined the expression patterns of all known classes of ADH in mouse embryonic and adult tissues, and also measured retinoic acid levels. Using in situ hybridization, class I ADH mRNA was localized in the embryo to the epithelia of the genitourinary tract, intestinal tract, adrenal gland, liver, conjunctival sac, epidermis, nasal epithelium, and lung, plus in the adult to epithelia within the testis, epididymis, uterus, kidney, intestine, adrenal cortex, and liver. Class IV ADH mRNA was localized in the embryo to the adrenal gland and nasal epithelium, plus in the adult to the epithelia of the esophagus, stomach, testis, epididymis, epidermis, and adrenal cortex. Class III ADH mRNA, in contrast, was present at low levels and not highly localized in the embryonic and adult tissues examined. We detected significant retinoic acid levels in the fetal kidney, fetal/adult intestine and adrenal gland, as well as the adult liver, lung, testis, epididymis, and uterus--all sites of class I and/or class IV ADH gene expression. These findings indicate that the expression patterns of class I ADH and class IV ADH, but not class III ADH, are consistent with a function in local retinoic acid synthesis needed for the development and maintenance of many specialized epithelial tissues.
维生素A(视黄醇)通过代谢生成视黄酸来调节胚胎发育和成年上皮功能,视黄酸是一种基因表达的多效性调节因子。视黄酸在局部合成并以自分泌或旁分泌方式发挥作用,但其中涉及的酶仍不清楚。能够代谢视黄醇的酒精脱氢酶(ADH)同工酶包括I类和IV类ADH,而III类ADH无此功能。ADH也代谢乙醇,高浓度乙醇会抑制视黄醇代谢,这提示了酒精中毒某些医学并发症的一种可能作用方式。为探究是否有任何ADH同工酶与视黄酸合成有关,我们在此研究了所有已知类别的ADH在小鼠胚胎和成年组织中的表达模式,并测定了视黄酸水平。通过原位杂交,I类ADH mRNA在胚胎中定位于泌尿生殖道、肠道、肾上腺、肝脏、结膜囊、表皮、鼻上皮和肺的上皮细胞,在成体中定位于睾丸、附睾、子宫、肾脏、肠道、肾上腺皮质和肝脏内的上皮细胞。IV类ADH mRNA在胚胎中定位于肾上腺和鼻上皮,在成体中定位于食管、胃、睾丸、附睾、表皮和肾上腺皮质的上皮细胞。相比之下,III类ADH mRNA在检测的胚胎和成年组织中水平较低且定位不明显。我们在胎儿肾脏、胎儿/成年肠道和肾上腺以及成年肝脏、肺、睾丸、附睾和子宫中检测到了显著的视黄酸水平,这些都是I类和/或IV类ADH基因表达的部位。这些发现表明,I类ADH和IV类ADH而非III类ADH的表达模式,与许多特殊上皮组织发育和维持所需的局部视黄酸合成功能一致。