Circ_0004354 might compete with circ_0040039 to induce NPCs death and inflammatory response by targeting miR-345-3p-FAF1/TP73 axis in intervertebral disc degeneration

Author:

Li Yongjin12ORCID,Wu Xiaojing3,Li Jianhua4,Du Lilong12,Wang Xuke5,Cao Jiasong6,Li Hao12,Huo Zhenxin12,Li Guowang12,Pan Dayu2,Xu Haiwei12,Xu Baoshan12ORCID

Affiliation:

1. Department of Minimally Invasive Spine Surgery, Tianjin Hospital, 406. No, Jiefangnan Road, Hexi district, Tianjin, 300211, China

2. Graduate School, Tianjin Medical University, 22 Qixiangtai Road, Tianjin 300070, China

3. Department of Surgery Critical Care Medicine, Beijing Shijitan Hospital, Capital Medical University, No. 10 Tieyi Road, Haidian District, Beijing 100038, China

4. Department of Orthopaedics, Tianjin Haihe Hospital, Tianjin 300350, China

5. Department of Minimally Invasive Spine Surgery, Luoyang Orthopedic-Traumatological Hospital, QiMing Road, LuoYang city, 471002, China

6. Tianjin key lab of human development and reproductive regulation, Tianjin Central Hospital of Obstetrics and Gynecology, Nankai University, Tianjin 300199, China

Abstract

The abnormal function of nucleus pulposus cells (NPCs) plays a crucial role in the pathogenesis of intervertebral disc degeneration (IVDD). Recent studies have demonstrated that circular RNAs (circRNAs) are involved in the pathological process of IVDD by regulating NPCs’ function. Nevertheless, the investigation on circRNA-circRNA interaction has not yet been reported. Here, we identified the top upregulated circ_0040039 and circ_0004354 in IVDD, derived from the syntrophin beta 2 gene but had different degrees of biological functions. Accumulating studies have reported PANoptosis is composed of apoptosis, pyroptosis, and necroptosis. Based on this, we think there should be a new pro-inflammatory cell death PAoptosis in the form of apoptosis and pyroptosis. Circ_0004354 might compete with circ_0040039 to induce the development of IVDD by modulating miR-345-3p-FAF1/TP73 axis-mediated PAoptosis, inflammatory response, growth inhibition, and ECM degradation of NPCs. Thus, these findings offer a novel insight into the circRNAs-mediated posttranscriptional regulatory network in IVDD, contributing to further clarification of the pathological mechanism of IVDD to develop a promising therapeutic target for IVDD diseases.

Funder

National Natural Science Foundation of China

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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