Ruth L. and David S. Gottesman Institute for Stem Cell and Regenerative Medicine Research, Albert Einstein College of Medicine, New York, New York, USA.
Nat Med. 2013 Jun;19(6):695-703. doi: 10.1038/nm.3155. Epub 2013 May 5.
Anticancer chemotherapy drugs challenge hematopoietic tissues to regenerate but commonly produce long-term sequelae. Chemotherapy-induced deficits in hematopoietic stem or stromal cell function have been described, but the mechanisms mediating hematopoietic dysfunction remain unclear. Administration of multiple cycles of cisplatin chemotherapy causes substantial sensory neuropathy. Here we demonstrate that chemotherapy-induced nerve injury in the bone marrow of mice is a crucial lesion impairing hematopoietic regeneration. Using pharmacological and genetic models, we show that the selective loss of adrenergic innervation in the bone marrow alters its regeneration after genotoxic insult. Sympathetic nerves in the marrow promote the survival of constituents of the stem cell niche that initiate recovery. Neuroprotection by deletion of Trp53 in sympathetic neurons or neuroregeneration by administration of 4-methylcatechol or glial-derived neurotrophic factor (GDNF) promotes hematopoietic recovery. These results demonstrate the potential benefit of adrenergic nerve protection for shielding hematopoietic niches from injury.
抗癌化疗药物促使造血组织再生,但通常会产生长期的后遗症。已经描述了化疗引起的造血干/基质细胞功能缺陷,但介导造血功能障碍的机制仍不清楚。多次顺铂化疗会导致明显的感觉性周围神经病。在这里,我们证明了化疗引起的小鼠骨髓神经损伤是一种严重的病变,会损害造血再生。通过药理学和遗传学模型,我们表明骨髓中肾上腺素能神经支配的选择性丧失会改变其在基因毒性损伤后的再生。骨髓中的交感神经促进启动恢复的干细胞龛成分的存活。交感神经元中 Trp53 的缺失或 4-甲基儿茶酚或胶质衍生神经营养因子 (GDNF) 的神经再生可促进造血恢复。这些结果表明,保护肾上腺素能神经有助于保护造血龛免受损伤,具有潜在的益处。