DOI: 10.1097/phm.0000000000002488 ISSN: 1537-7385

Tnfaip8 and Tipe2 Gene Deletion Ameliorates Immediate Proteoglycan Loss and Inflammatory Responses in the Injured Mouse Intervertebral Disc

Jiawei Lu, Zuozhen Tian, Frances S. Shofer, Ling Qin, Honghong Sun, Yejia Zhang
  • Rehabilitation
  • Physical Therapy, Sports Therapy and Rehabilitation
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Abstract

OBJECTIVE

TNFAIP8 and TIPE2 belong to TNFa-induced protein 8 (TNFAIP8/TIPE) family. They control apoptosis and direct leukocyte migration. Nucleus pulposus (NP) cell loss is a hallmark of intervertebral disc (IVD) degeneration in response to injury, and inflammation may cause pain. Here, we examined the effects of TNFAIP8/TIPE2 deficiency on the IVDs in mice with these genes deleted.

Design

Tail IVDs in Tnfaip8 or Tipe2 single and double knockout mice (Tnfaip8-/- , Tipe2-/- , and Tnfaip8/Tipe2 dko), and wild type (WT) controls were injured. The spine motion segments were stained with Safranin O to reveal proteoglycans. Macrophages were identified by immunostaining, and selected inflammatory marker and collagen gene expression was examined by Real Time PCR.

RESULTS

The injured tail IVDs of Tnfaip-/- , Tipe2-/- , and Tnfaip8/Tipe2 dko mice all displayed higher levels of proteoglycans than WT controls. Fewer macrophages were found in the injured IVDs of Tipe2-/- and Tnfaip8/Tipe2 dko mice than WT. Il6, Adam8 and Col1 gene expression was downregulated in the injured IVDs of Tnfip8/Tipe2 dko mice.

CONCLUSIONS

TNFAIP8 and TIPE2 loss of function ameliorated proteoglycan loss and inflammation in the injured IVDs. They may serve as molecular targets to preserve disc structure and reduce inflammation.

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