Lehmann S, Paul C, Törmä H
Department of Hematology, Karolinska Institute, Huddinge Hospital, Stockholm, Sweden.
Leuk Lymphoma. 2002 Apr;43(4):851-8. doi: 10.1080/10428190290016999.
Retinoic acid (RA) has important effects on cell differentiation and cell growth and on normal embryonic development. Intracellular retinoid signaling induced by endogenous or exogenous RA is regulated by retinoid binding proteins such as CRBPI, CRABPI and CRABPII and there are data suggesting that the expression of these proteins can influence the sensitivity to the growth inhibitory effects of ATRA. In this study, we investigated the basal and ATRA-induced expression of CRBPI and CRABPI and II in leukemic cell lines and in cells from patients with acute myeloid leukemia (AML). CRBPI as well as CRABPI and II were expressed in all tested cell lines and in leukemic cells from all 18 AML-patients. CRABPII mRNA expression was more abundant than CRBPI and CRABPI in both the cell lines and the patient cells but the levels compared the house keeping gene was lower in the patient cells. In all cell lines and in 69% of the patient samples, ATRA did upregulate CRABPII whereas CRBPI exhibited a varying response and CRABPI was more commonly downregulated. The sensitivity to the growth inhibitory effects of ATRA did not correlate with the basal expression of any of these proteins. However, ATRA-induced upregulation of CRABPII did significantly correlate with the ATRA sensitivity (p < 0.005) as well as with ATRA-induced upregulation of the retinoid receptor RARbeta (p < 0.05). We conclude that the retinoid binding proteins CRBPI and CRABPI and II are expressed in myeloid leukemic cells of non-M3 type but that the level of expression does not affect ATRA sensitivity.
维甲酸(RA)对细胞分化、细胞生长及正常胚胎发育具有重要作用。内源性或外源性RA诱导的细胞内类视黄醇信号传导受类视黄醇结合蛋白如CRBPI、CRABPI和CRABPII的调节,有数据表明这些蛋白的表达可影响对全反式维甲酸(ATRA)生长抑制作用的敏感性。在本研究中,我们调查了CRBPI、CRABPI和CRABPII在白血病细胞系及急性髓性白血病(AML)患者细胞中的基础表达及ATRA诱导的表达情况。CRBPI以及CRABPI和CRABPII在所有测试的细胞系及18例AML患者的白血病细胞中均有表达。在细胞系和患者细胞中,CRABPII mRNA表达均比CRBPI和CRABPI丰富,但与管家基因相比,患者细胞中的水平较低。在所有细胞系及69%的患者样本中,ATRA确实上调了CRABPII,而CRBPI表现出不同的反应,CRABPI更常见下调。对ATRA生长抑制作用的敏感性与这些蛋白的基础表达均无相关性。然而,ATRA诱导的CRABPII上调与ATRA敏感性显著相关(p < 0.005),也与ATRA诱导的类视黄醇受体RARβ上调相关(p < 0.05)。我们得出结论,类视黄醇结合蛋白CRBPI、CRABPI和CRABPII在非M3型髓性白血病细胞中表达,但表达水平不影响ATRA敏感性。