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Tendon stem/progenitor cells regulate inflammation in tendon healing via JNK and STAT3 signaling.
Tarafder, Solaiman; Chen, Esther; Jun, Yena; Kao, Kristy; Sim, Kun Hee; Back, Jungho; Lee, Francis Y; Lee, Chang H.
Afiliação
  • Tarafder S; Regenerative Engineering Laboratory, Columbia University Irving Medical Center, New York, New York, USA.
  • Chen E; Regenerative Engineering Laboratory, Columbia University Irving Medical Center, New York, New York, USA.
  • Jun Y; Regenerative Engineering Laboratory, Columbia University Irving Medical Center, New York, New York, USA.
  • Kao K; Regenerative Engineering Laboratory, Columbia University Irving Medical Center, New York, New York, USA.
  • Sim KH; Regenerative Engineering Laboratory, Columbia University Irving Medical Center, New York, New York, USA.
  • Back J; Department of Orthopaedics and Rehabilitation, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Lee FY; Department of Orthopaedics and Rehabilitation, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Lee CH; Regenerative Engineering Laboratory, Columbia University Irving Medical Center, New York, New York, USA; chl2109@cumc.columbia.edu.
FASEB J ; 31(9): 3991-3998, 2017 09.
Article em En | MEDLINE | ID: mdl-28533328
Tendon stem/progenitor cells (TSCs) have been found in different anatomic locations and showed a promising regenerative potential. We identified a role of TSCs in the regulation of inflammation during healing of acute tendon injuries. Delivery of connective tissue growth factor (CTGF) into full-transected rat patellar tendons significantly increased the number of CD146+ TSCs, leading to enhanced healing. In parallel, CTGF delivery significantly reduced the number of iNOS+ M1 macrophages and increased the expression of anti-inflammatory IL-10 at 2 d after surgery, with over 85% CD146+ TSCs expressing IL-10. By 1 wk, the elevated IL-10 expression remained, and IL-6 expression was significantly attenuated in CTGF-delivered tendon healing. Matrix metalloproteinase (MMP)-3 expression in CTGF-delivered tendon was organized along with the reorienting collagen fibers by 1 wk after surgery, in comparison with the control group showing the abundant MMP-3 expression localized at healing junction. Tissue inhibitor of metalloprotease (TIMP)-3 was expressed in CD146+ TSCs at 1 wk with CTGF, in contrast to control with no TIMP-3 expression. In vitro, IL-10 expression was detected only when tendon cells were stimulated with IL-1ß, and CTGF and significantly higher in CD146+ TSCs than CD146- tendon cells. Similarly, TIMP-3 expression was detected only when treated with CTGF or CTGF and IL-1ß that is significantly higher in CD146+ TSCs compared to CD146- tendon cells. Signaling study with specific inhibitors and Western blot analysis demonstrated that CTGF-induced expression of IL-10 and TIMP-3 in CD146+ TSCs are regulated by JNK/signal transducer and activator of transcription 3 signaling. Taken together, these findings suggest anti-inflammatory roles of CTGF-stimulated TSCs that are likely associated with improved tendon healing.-Tarafder, S., Chen, E., Jun, Y., Kao, K., Sim, K. H., Back, J., Lee, F. Y., Lee, C. H. Tendon stem/progenitor cells regulate inflammation in tendon healing via JNK and STAT3 signaling.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tendões / MAP Quinase Quinase 4 / Fator de Transcrição STAT3 / Inflamação Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tendões / MAP Quinase Quinase 4 / Fator de Transcrição STAT3 / Inflamação Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2017 Tipo de documento: Article