Department of Pathology, Division of Neuropathology, University of Rochester Medical Center, Rochester, NY, USA.
Int J Radiat Biol. 2012 Jul;88(7):547-55. doi: 10.3109/09553002.2012.690929. Epub 2012 May 25.
The pathogenesis of meningiomas remains largely unknown, but there is evidence that exposure radiation increases the risk of meningiomas. We therefore evaluated whether radiation stimulates human leptomeningeal cell proliferation and activates growth regulatory pathways.
Cultures from six human primary leptomeningeal cells were established and irradiated with 0.5, 1 or 2 Gy. Cells were subsequently maintained for approximately 3-6 months and then treated with the mitogen, platlet-derived growth factor-BB (PDGF-BB), or human cerebrospinal fluid (CSF) obtained from patients with no neurological disease. Cell proliferation was evaluated by CyQUANT, and changes in the regulatory activation levels of signal transducer and activator of transcription (STAT3), mitogen-activated protein kinase kinase 1/2 (MEK1/2), mitogen activated protein kinase (MAPK 44/42), Akt, and mammalian target of rapamycin (mTOR) were assessed by Western blot.
At both 3 and 6 months post-irradiation, CSF stimulated cell proliferation in all six leptomeningeal cultures. At 3 months, radiation was associated with an increase in STAT3, MEK 1/2, p44/42 MAPK and variable Akt activation, and at 6 months, STAT3, p44/42 MAPK, variable Akt and mTOR activation was observed in response to PDGF-BB and CSF.
Irradiation of fetal leptomeningeal cells was associated with loss of heterozygosity of 1p36 and persistent sensitization leading to upregulation in growth pathways in response to PDGF and CSF. These findings suggest a mechanistic basis for radiation's role in meningioma initiation.
脑膜瘤的发病机制仍不清楚,但有证据表明,暴露于辐射会增加脑膜瘤的风险。因此,我们评估了辐射是否会刺激人软脑膜细胞增殖并激活生长调节途径。
从六个人类原发性软脑膜细胞中培养并以 0.5、1 或 2 Gy 照射。细胞随后被维持大约 3-6 个月,然后用有丝分裂原血小板衍生生长因子-BB (PDGF-BB) 或从无神经疾病患者获得的人脑脊液 (CSF) 处理。通过 CyQUANT 评估细胞增殖,并通过 Western blot 评估信号转导和转录激活因子 (STAT3)、丝裂原激活蛋白激酶激酶 1/2 (MEK1/2)、丝裂原激活蛋白激酶 (MAPK 44/42)、Akt 和哺乳动物雷帕霉素靶蛋白 (mTOR) 的调节激活水平的变化。
在照射后 3 个月和 6 个月,CSF 刺激了所有六种软脑膜培养物中的细胞增殖。在 3 个月时,辐射与 STAT3、MEK1/2、p44/42 MAPK 和可变 Akt 激活增加有关,而在 6 个月时,PDGF-BB 和 CSF 刺激观察到 STAT3、p44/42 MAPK、可变 Akt 和 mTOR 激活。
胎儿软脑膜细胞的照射与 1p36 的杂合性缺失和持续敏化有关,导致对 PDGF 和 CSF 的生长途径的上调。这些发现为辐射在脑膜瘤起始中的作用提供了机制基础。