Keay Susan K, Szekely Zoltan, Conrads Thomas P, Veenstra Timothy D, Barchi Joseph J, Zhang Chen-Ou, Koch Kristopher R, Michejda Christopher J
Division of Infectious Diseases, Department of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Proc Natl Acad Sci U S A. 2004 Aug 10;101(32):11803-8. doi: 10.1073/pnas.0404509101. Epub 2004 Jul 28.
Approximately 1 million people in the United States suffer from interstitial cystitis, a chronic painful urinary bladder disorder characterized by thinning or ulceration of the bladder epithelial lining; its etiology is unknown. We have identified a glycosylated frizzled-related peptide inhibitor of cell proliferation that is secreted specifically by bladder epithelial cells from patients with this disorder. This antiproliferative factor (APF) profoundly inhibits bladder cell proliferation by means of regulation of cell adhesion protein and growth factor production. The structure of APF was deduced by using ion trap mass spectrometry (MS), enzymatic digestion, lectin affinity chromatography, and total synthesis, and confirmed by coelution of native and synthetic APF derivatives on microcapillary reversed-phase liquid chromatography (microRPLC)/MS. APF was determined to be an acidic, heat-stable sialoglycopeptide whose peptide chain has 100% homology to the putative sixth transmembrane domain of frizzled 8. Both synthetic and native APF had identical biological activity in normal bladder epithelial cells and T24 bladder cancer cells. Northern blot analysis indicated binding of a probe containing the sequence for the frizzled 8 segment with mRNA extracted from cells of patients with interstitial cystitis but not controls. APF is therefore a frizzled-related peptide growth inhibitor shown to contain exclusively a transmembrane segment of a frizzled protein and is a potential biomarker for interstitial cystitis.
美国约有100万人患有间质性膀胱炎,这是一种慢性疼痛性膀胱疾病,其特征是膀胱上皮内层变薄或溃疡;其病因尚不清楚。我们已经鉴定出一种细胞增殖的糖基化卷曲相关肽抑制剂,它由患有这种疾病的患者的膀胱上皮细胞特异性分泌。这种抗增殖因子(APF)通过调节细胞粘附蛋白和生长因子的产生,深刻地抑制膀胱细胞增殖。通过离子阱质谱(MS)、酶消化、凝集素亲和色谱和全合成推导了APF的结构,并通过微毛细管反相液相色谱(microRPLC)/MS上天然和合成APF衍生物的共洗脱进行了确认。APF被确定为一种酸性、热稳定的唾液酸糖肽,其肽链与卷曲蛋白8的假定第六跨膜结构域具有100%的同源性。合成APF和天然APF在正常膀胱上皮细胞和T24膀胱癌细胞中具有相同的生物学活性。Northern印迹分析表明,含有卷曲蛋白8片段序列的探针与从间质性膀胱炎患者而非对照组的细胞中提取的mRNA结合。因此,APF是一种卷曲相关肽生长抑制剂,仅显示含有卷曲蛋白的一个跨膜片段,并且是间质性膀胱炎的潜在生物标志物。