Chiao J H, Roy K, Tolner B, Yang C H, Sirotnak F M
Molecular Pharmacology and Therapeutics Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
J Biol Chem. 1997 Apr 25;272(17):11165-70. doi: 10.1074/jbc.272.17.11165.
Mediated folate compound transport inward in isolated luminal epithelial cells from mouse small intestine was delineated as pH-dependent and non-pH-dependent components on the basis of their differential sensitivity to the stilbene inhibitor, 4, 4'-diisothiocyanatostilbene-2,2'-disulfonic acid. pH dependence was manifested as higher maximum capacity (Vmax) for influx of l, L-5-CH3-H4folate at acidic pH compared with neutral or alkaline pH with no effect on saturability (Km). The pH-dependent component was relatively insensitive to inhibition by 4, 4'-diisothiocyanatostilbene-2,2'-disulfonic acid and highly saturable (Km or Ki = 2 to 4 microM) in the case of folic acid, folate coenzymes, and 4-aminofolate analogues as permeants or inhibitors. The non-pH-dependent component was highly sensitive to 4, 4'-diisothiocyanatostilbene-2,2'-disulfonic acid and poorly and variably saturable (Km or Ki = 20 to >2000 microM) with respect to these folate compounds. Only the pH-dependent transport component was developmentally regulated, showing much higher maximum capacity for l,L-5-CH3-H4folate influx in mature absorptive rather than proliferative crypt cells. The increase in pH-dependent influx during maturation was associated with an increase in RFC-1 gene expression in the form of a 2.5-kilobase RNA transcript and 58-kDa brush-border membrane protein detected by folate-based affinity labeling and with anti-mouse RFC-1 peptide antibodies. The size of this protein was the same as that encoded by RFC-1 mRNA. The treatment of mature absorptive cells with either the affinity label or the anti-RFC-1 peptide antibodies inhibited influx of l, L-[3H]-5-CH3-H4folate in a concentration-dependent manner. These results strongly suggest that pH-dependent folate absorption in this tissue is regulated by RFC-1 gene expression.
基于对二苯乙烯抑制剂4,4'-二异硫氰基二苯乙烯-2,2'-二磺酸的不同敏感性,从小鼠小肠分离的腔上皮细胞中介导的叶酸化合物向内转运被划分为pH依赖性和非pH依赖性成分。pH依赖性表现为与中性或碱性pH相比,在酸性pH下l,L-5-CH3-H4叶酸流入的最大容量(Vmax)更高,而对饱和性(Km)没有影响。pH依赖性成分对4,4'-二异硫氰基二苯乙烯-2,2'-二磺酸的抑制相对不敏感,对于叶酸、叶酸辅酶和4-氨基叶酸类似物作为渗透剂或抑制剂的情况,其具有高度饱和性(Km或Ki = 2至4 microM)。非pH依赖性成分对4,4'-二异硫氰基二苯乙烯-2,2'-二磺酸高度敏感,对于这些叶酸化合物,其饱和性较差且变化较大(Km或Ki = 20至>2000 microM)。只有pH依赖性转运成分受到发育调控,在成熟的吸收性而非增殖性隐窝细胞中,l,L-5-CH3-H4叶酸流入的最大容量要高得多。成熟过程中pH依赖性流入的增加与RFC-1基因表达的增加相关,通过基于叶酸的亲和标记和抗小鼠RFC-1肽抗体检测到的2.5千碱基RNA转录本和58-kDa刷状缘膜蛋白的形式。该蛋白的大小与RFC-1 mRNA编码的大小相同。用亲和标记或抗RFC-1肽抗体处理成熟的吸收性细胞,以浓度依赖性方式抑制l,L-[3H]-5-CH3-H4叶酸的流入。这些结果强烈表明,该组织中pH依赖性叶酸吸收受RFC-1基因表达调控。