共 56 条
PPP1CC is associated with astrocyte and microglia proliferation after traumatic spinal cord injury in rats
被引:15
作者:
Liu, Xiaojuan
[1
,7
]
Huang, Shen
[2
,7
]
Liu, Chun
[4
,7
]
Liu, Xia
[5
,7
]
Shen, Yuntian
[6
]
Cui, Zhiming
[3
,7
]
机构:
[1] Nantong Univ, Med Coll, Dept Pathogen Biol, Nantong 226001, Jiangsu, Peoples R China
[2] First People Hosp Changsha, Dept Osteol, Changsha 226001, Jiangsu, Peoples R China
[3] People Hosp Nantong, Dept Osteol, Nantong 226001, Jiangsu, Peoples R China
[4] Nantong Univ, Lab Anim Ctr, Nantong 226001, Jiangsu, Peoples R China
[5] Nantong Univ, Med Coll, Dept Pathophysiol, Narttong 226001, Jiangsu, Peoples R China
[6] Nantong Univ, Dept Coinnovat Ctr Neuroregenerat, Nantong 226000, Jiangsu, Peoples R China
[7] Nantong Univ, Med Coll, Jiangsu Prov Key Lab Inflammat & Mol Drug Target, Nantong 226001, Jiangsu, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Spinal cord injury;
Protein phosphatase 1;
Catalytic subunit;
Gamma isozyme (PPP1CC);
Astrocyte;
Microglia;
Proliferation;
Rats;
MAMMALIAN PEROXIREDOXIN;
PHOSPHATASE;
ACTIVATION;
NEURON;
IDENTIFICATION;
KINASE;
PHOSPHORYLATION;
REGENERATION;
INVOLVEMENT;
TYPE-1;
D O I:
10.1016/j.prp.2017.09.020
中图分类号:
R36 [病理学];
学科分类号:
100103 [病原生物学];
摘要:
Reactive astrogliosis and microgliosis after spinal cord injury (SCI) contribute to glial scar formation that impedes axonal regeneration. The mechanisms underlying reactive astrocyte and microglia proliferation upon injury remain partially understood. Protein phosphatase 1, catalytic subunit, gamma isozyme (PPP1CC) participates in cell proliferation, differentiation and apoptosis. However, the expression and functions of PPP1CC following SCI are still unknown. In this study, an acute spinal cord contusion injury model in adult rats was established to investigate the potential role of PPP1CC during the pathological process of SCI. The palpable expression increase of PPP1CC after SCI was found by western blot and immunohistochemistry staining. Double immunofluorescence staining showed that PPP1CC expression mainly increased in astrocytes and microglia, as well as PPP1CC and proliferating cell nuclear antigen (PCNA) co-localized in astrocytes and microglia. Furthermore, PCNA expression also elevated after SCI in a similar manner as PPP1CC. In vitro, PPP1CC and PCNA expression in primary rat spinal cord astrocytes and microglia changed in a similar concentration-and time-dependent manner according to LPS treatment. In addition, PPP1CC knockdown in astrocytes and microglia resulted in the decrease of PCNA expression and the number of Brdu positive cells after LPS stimulation, showing that PPP1CC promoted astrocyte and microglia proliferation after inflammation. In a word, PPP1CC might be associated with astrocyte and microglia proliferation after SCI, implying that PPP1CC is a potential molecular target for the therapy of SCI.
引用
收藏
页码:1355 / 1364
页数:10
相关论文

