Cellular Senescence Is Induced by the Environmental Neurotoxin Paraquat and Contributes to Neuropathology Linked to Parkinson's Disease

被引:460
作者
Chinta, Shankar J. [1 ,4 ]
Woods, Georgia [1 ]
Demaria, Marco [1 ,5 ]
Rane, Anand [1 ]
Zou, Ying [1 ]
McQuade, Amanda [1 ]
Rajagopalan, Subramanian [1 ]
Limbad, Chandani [1 ,2 ]
Madden, David T. [1 ,4 ]
Campisi, Judith [1 ,3 ]
Andersen, Julie K. [1 ]
机构
[1] Buck Inst Res Aging, 8001 Redwood Blvd, Novato, CA 94945 USA
[2] Univ Calif Berkeley, Comparat Biochem Grad Program, Berkeley, CA 94720 USA
[3] Lawrence Berkeley Natl Lab, 1 Cyclotron Rd, Berkeley, CA 94720 USA
[4] Touro Univ Calif, Coll Pharm, 1310 Club Dr, Vallejo, CA 94592 USA
[5] Univ Groningen, Univ Med Ctr Groningen, European Inst Biol Aging ERIBA, NL-9700 AD Groningen, Netherlands
关键词
CELLS; STRESS; NEUROGENESIS; RESISTANT; BARRIER; DAMAGE; MODEL; RISK; P53;
D O I
10.1016/j.celrep.2017.12.092
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Exposure to the herbicide paraquat (PQ) is associated with an increased risk of idiopathic Parkinson's disease (PD). Therapies based on PQ's presumed mechanisms of action have not, however, yielded effective disease therapies. Cellular senescence is an anticancer mechanism that arrests proliferation of replication-competent cells and results in a pro-inflammatory senescence-associated secretory phenotype (SASP) capable of damaging neighboring tissues. Here, we demonstrate that senescent cell markers are preferentially present within astrocytes in PD brain tissues. Additionally, PQ was found to induce astrocytic senescence and an SASP in vitro and in vivo, and senescent cell depletion in the latter protects against PQ-induced neuropathology. Our data suggest that exposure to certain environmental toxins promotes accumulation of senescent cells in the aging brain, which can contribute to dopaminergic neurodegeneration. Therapies that target senescent cells may constitute a strategy for treatment of sporadic PD, for which environmental exposure is a major risk factor.
引用
收藏
页码:930 / 940
页数:11
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