Alexandrescu Sanda, Tatevian Nina, Czerniak Bogdan A, Covinsky Michael H, Burns Nadja K, Brown Robert E
Department of Pathology, University of Texas at Houston-Health Science Center, Houston, TX 77030, USA.
Int J Clin Exp Pathol. 2012;5(6):503-11. Epub 2012 Jul 29.
Langerhans cell histiocytosis (LCH) has a challenging and still unclear pathogenesis. A body of literature points to impaired maturation of the lesional dendritic cells, and to immune dysregulation in the form of increased FoxP3 cells. Various cytokine abnormalities such as expression of transforming growth factor (TGF)-β have been reported, as well as abnormalities in lipid content in LCH cells. Morphoproteomic techniques were applied to identify the signal transduction pathways that could influence histogenesis and immune regulation in osteolytic LCH. Five pediatric cases of osteolytic LCH were examined, using antibodies against CD1a, S100, CD68, CD8, FoxP3, phosphorylated (p)-STAT3 (Tyr705), protein kinase C (PKC)-α, phospholipase (PL)D1, fatty acid synthase (FASN), and zinc finger protein, Gli2. Positive and negative controls were performed. A FoxP3(+)/CD8(+) cell ratio was calculated by counting the FoxP3+ and CD8+ cells in 10 high power fields for each case. There is induction of sonic hedgehog (SHH) mediators consistent with TGF-β signaling pathway through Smad3-dependent activation of Gli2, findings supported by the plasmalemmal and cytoplasmic expression of PKC-α and PLD1, and nuclear expression of Gli2, in lesional cells. The FoxP3+/CD8+ cell ratio is increased, ranging from 1.7-7.94. There is moderate cytoplasmic expression of FASN in most of the Langerhans cells, a finding that supports previously published phospholipid abnormalities in LCH and is consistent with PKC-α/PLD1/TGF-β signaling. With our study, we strongly suggest that the TGF-β cell signaling pathway is a major player in the pathogenesis of LCH, leading to non-canonical induction of nuclear Gli2 expression, thereby contributing to osteoclastogenesis in LCH histiocytes. It could also cause a state of immune frustration in LCH, by inducing the transformation of CD4(+)CD25(-) cells into CD4(+)/FoxP3(+) cells. This coincides with the clinical evidence of a response to thalidomide in patients with osteolytic LCH, given its reported ability to reduce TGF-beta 1 and FoxP3 cells. Such TGF-β signaling in osteoclastogenesis and immune dysregulation, and the presence of FASN in the majority of cells, have additional therapeutic implications for osteolytic LCH.
朗格汉斯细胞组织细胞增多症(LCH)的发病机制具有挑战性且仍不清楚。大量文献指出病变树突状细胞成熟受损,以及以FoxP3细胞增加形式出现的免疫失调。已报道了各种细胞因子异常,如转化生长因子(TGF)-β的表达,以及LCH细胞中脂质含量的异常。应用形态蛋白质组学技术来识别可能影响溶骨性LCH组织发生和免疫调节的信号转导途径。对5例儿童溶骨性LCH病例进行了检查,使用了针对CD1a、S100、CD68、CD8、FoxP3、磷酸化(p)-STAT3(Tyr705)、蛋白激酶C(PKC)-α、磷脂酶(PL)D1、脂肪酸合酶(FASN)和锌指蛋白Gli2的抗体。进行了阳性和阴性对照。通过计算每个病例10个高倍视野中的FoxP3+和CD8+细胞来计算FoxP3(+)/CD8(+)细胞比率。在病变细胞中,通过Smad3依赖性激活Gli2诱导了与TGF-β信号通路一致的音猬因子(SHH)介质,PKC-α和PLD1的质膜和细胞质表达以及Gli2的核表达支持了这一发现。FoxP3+/CD8+细胞比率增加,范围为1.7 - 7.94。大多数朗格汉斯细胞中FASN呈中度细胞质表达,这一发现支持了先前发表的LCH中磷脂异常,并与PKC-α/PLD1/TGF-β信号传导一致。通过我们的研究,我们强烈认为TGF-β细胞信号通路是LCH发病机制中的主要参与者,导致核Gli2表达的非经典诱导,从而促进LCH组织细胞中的破骨细胞生成。它还可能通过诱导CD4(+)CD25(-)细胞转化为CD4(+)/FoxP3(+)细胞而导致LCH中的免疫失调状态。这与溶骨性LCH患者对沙利度胺有反应的临床证据一致,因为据报道沙利度胺能够减少TGF-β1和FoxP3细胞。这种破骨细胞生成和免疫失调中的TGF-β信号传导,以及大多数细胞中FASN的存在,对溶骨性LCH具有额外的治疗意义。