Vella Antonio, D'Aversa Elisabetta, Api Martina, Breveglieri Giulia, Allegri Marisole, Giacomazzi Alice, Marinelli Busilacchi Elena, Fabrizzi Benedetta, Cestari Tiziana, Sorio Claudio, Bedini Gloria, D'Amico Giovanna, Bronte Vincenzo, Poloni Antonella, Benedetti Antonio, Bovo Chiara, Corey Seth J, Borgatti Monica, Cipolli Marco, Bezzerri Valentino
Unit of Immunology, Azienda Ospedaliera Universitaria Integrata, 37134 Verona, Italy.
Department of Life Sciences and Biotechnology, University of Ferrara, 44100 Ferrara, Italy.
Cancers (Basel). 2020 Mar 5;12(3):597. doi: 10.3390/cancers12030597.
Shwachman-Diamond syndrome (SDS) is a rare inherited bone marrow failure syndrome, resulting in neutropenia and a risk of myeloid neoplasia. A mutation in a ribosome maturation factor accounts for almost all of the cases. Lymphoid involvement in SDS has not been well characterized. We recently reported that lymphocyte subpopulations are reduced in SDS patients. We have also shown that the mTOR-STAT3 pathway is hyper-activated in SDS myeloid cell populations. Here we show that mTOR-STAT3 signaling is markedly upregulated in the lymphoid compartment of SDS patients. Furthermore, our data reveal elevated IL-6 levels in cellular supernatants obtained from lymphoblasts, bone marrow mononuclear and mesenchymal stromal cells, and plasma samples obtained from a cohort of 10 patients. Of note, everolimus-mediated inhibition of mTOR signaling is associated with basal state of phosphorylated STAT3. Finally, inhibition of mTOR-STAT3 pathway activation leads to normalization of IL-6 expression in SDS cells. Altogether, our data strengthen the hypothesis that SDS affects both lymphoid and myeloid blood compartment and suggest everolimus as a potential therapeutic agent to reduce excessive mTOR-STAT3 activation in SDS.
施瓦赫曼-戴蒙德综合征(SDS)是一种罕见的遗传性骨髓衰竭综合征,可导致中性粒细胞减少和发生髓系肿瘤的风险。核糖体成熟因子的突变几乎导致了所有病例。SDS中淋巴细胞受累情况尚未得到充分描述。我们最近报道SDS患者的淋巴细胞亚群减少。我们还表明,mTOR-STAT3通路在SDS髓系细胞群体中过度激活。在此我们表明,mTOR-STAT3信号在SDS患者的淋巴区室中显著上调。此外,我们的数据显示,从10名患者队列中获取的淋巴母细胞、骨髓单个核细胞和间充质基质细胞的细胞上清液以及血浆样本中的IL-6水平升高。值得注意的是,依维莫司介导的mTOR信号抑制与磷酸化STAT3的基础状态相关。最后,抑制mTOR-STAT3通路激活可使SDS细胞中IL-6表达正常化。总之,我们的数据强化了SDS影响淋巴和髓系血液区室的假说,并提示依维莫司作为一种潜在治疗药物可减少SDS中过度的mTOR-STAT3激活。