Rittenhouse-Diakun K, Van Leengoed H, Morgan J, Hryhorenko E, Paszkiewicz G, Whitaker J E, Oseroff A R
Department of Dermatology, Roswell Park Cancer Institute, Buffalo, New York 14263, USA.
Photochem Photobiol. 1995 May;61(5):523-8. doi: 10.1111/j.1751-1097.1995.tb02356.x.
Endogenously generated protoporphyrin IX (PpIX) from exogenous ALA can be an effective photosensitizer. PpIX accumulation is inversely dependent on available intracellular iron, which is required for the conversion of PpIX to heme. Iron also is necessary for cell replication. Since iron can be toxic, intracellular iron levels are tightly controlled. Activated and proliferating cells respond to the demand for intracellular iron by upregulating membrane expression of the transferrin receptor (CD71) which is needed for iron uptake. We predicted that activated lymphocytes (CD71+) would preferentially accumulate PpIX because of their lower intracellular iron levels and because of competition for iron between ALA-induced heme production and cellular growth processes. Thus, the CD71+ cells could serve as PDT targets. Stimulation of human peripheral blood lymphocytes (PBL) with the mitogens, phytohemagglutinin A, concanavalin A and pokeweed prior to incubation with ALA results in PpIX accumulation correlating with level of activation. Activated lymphocytes expressing high levels of surface CD71 transferrin receptors generated more PpIX than those with low CD71 expression. Incubating activated cells in transferrin depleted medium (thereby decreasing the iron availability) further increased PpIX levels. Malignant, CD71+ T lymphocytes from a patient with cutaneous T-cell lymphoma (CTCL)/Sezary syndrome also accumulated increased PpIX levels in comparison to normal lymphocytes. PDT of activated lymphocytes and Sezary cells after ALA incubation demonstrated preferential killing compared to normal, unstimulated PBL. These findings suggest a possible mechanism for the selectivity of ALA PDT for activated CD71+ cells. They also indicate a clinical use for ALA-PDT in therapy directed towards the malignant lymphocytes in leukemias and lymphomas, and as animmunomodulatory agent.
外源性5-氨基酮戊酸(ALA)内源性生成的原卟啉IX(PpIX)可以成为一种有效的光敏剂。PpIX的积累与细胞内可利用的铁呈负相关,铁是PpIX转化为血红素所必需的。铁对于细胞复制也是必需的。由于铁可能具有毒性,细胞内铁水平受到严格控制。活化和增殖的细胞通过上调转铁蛋白受体(CD71)的膜表达来响应细胞内铁的需求,转铁蛋白受体是铁摄取所必需的。我们预测,活化的淋巴细胞(CD71+)会优先积累PpIX,这是因为它们细胞内铁水平较低,还因为ALA诱导的血红素生成与细胞生长过程之间存在铁的竞争。因此,CD71+细胞可作为光动力疗法(PDT)的靶点。在用ALA孵育之前,用丝裂原植物血凝素A、刀豆球蛋白A和商陆刺激人外周血淋巴细胞(PBL),会导致PpIX积累与活化水平相关。表达高水平表面CD71转铁蛋白受体的活化淋巴细胞比CD71表达低的淋巴细胞产生更多的PpIX。在转铁蛋白缺乏的培养基中孵育活化细胞(从而降低铁的可利用性)会进一步提高PpIX水平。与正常淋巴细胞相比,来自皮肤T细胞淋巴瘤(CTCL)/Sezary综合征患者的恶性CD71+ T淋巴细胞也积累了更高水平的PpIX。ALA孵育后对活化淋巴细胞和Sezary细胞进行PDT显示,与正常的、未受刺激的PBL相比,具有优先杀伤作用。这些发现提示了ALA-PDT对活化的CD71+细胞具有选择性的一种可能机制。它们还表明ALA-PDT在针对白血病和淋巴瘤中的恶性淋巴细胞的治疗中以及作为一种免疫调节剂具有临床应用价值。