Temporal and Spatial Expression of LGR5 After Acute Spinal Cord Injury in Adult Rats

被引:4
作者
Chen, Xiaoqing [1 ]
Hao, Jie [1 ,2 ]
Fu, Ting [3 ]
Liu, Jie [1 ,2 ]
Yu, Mingchen [1 ,2 ]
He, Shuang [4 ]
Qian, Rong [1 ,2 ]
Zhang, Feng [1 ]
机构
[1] Nantong Univ, Dept Orthoped, Affiliated Hosp, Nantong 226001, Jiangsu, Peoples R China
[2] Nantong Univ, Coll Med, Nantong 226001, Jiangsu, Peoples R China
[3] Nantong Univ, Sch Nursing, Nantong, Peoples R China
[4] Nantong Univ, Affiliated Hosp 2, Nantong 226001, Peoples R China
关键词
Spinal cord injury; LGR5; Astrocyte; Proliferation; ASTROGLIAL CELL-PROLIFERATION; STEM-CELLS; FUNCTIONAL RECOVERY; NEURONAL APOPTOSIS; REACTIVE GLIOSIS; DIFFERENTIATION; REGENERATION; PROTEIN; CONTRIBUTES; PRECURSORS;
D O I
10.1007/s11064-016-1977-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Leucine-rich repeat-containing G-protein coupled receptor 5 (LGR5), a well-characterized marker of stem cell and cancer stem cells (CSCs), is best known as a transmembrance receptor for increases canonical Wnt signaling amplitude. In addition, in some types of human cancers, LGR5 has been found to be overexpressed. However, the distribution and function of LGR5 in spinal cord injury (SCI) are still unknown. In this study, we examined LGR5 expression and cellular localization in rats following acute SCI. Western blot analysis and immunohistochemistry exhibited an important upregulation of LGR5 in injury spinal cord. Double immunofluorescence staining showed that LGR5 was co-expressed with glial fibrillary acidic protein (GFAP). Moreover, we detected that PCNA had colocalization with LGR5 and GFAP after SCI. In the vitro model, we could find the enhanced expression of LGR5 in the primary astrocyte which was induced by the lipopolysaccharide (LPS). In particular, we found the significantly decreased ability for proliferation when this LGR5-specific siRNA transfected primary astrocytes. In a word, this is the first description of LGR5 expression in spinal cord injury. These data indicated that LGR5 might be of great significance in CNS pathophysiology after SCI.
引用
收藏
页码:2645 / 2654
页数:10
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