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  • 2015-2019  (2)
  • Medicine  (2)
  • XA 30325  (2)
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  • 2015-2019  (2)
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  • Medicine  (2)
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  • 1
    In: Arthritis & Rheumatology, Wiley, Vol. 71, No. 2 ( 2019-02), p. 302-314
    Abstract: Several studies have demonstrated that the secreted glycoprotein and integrin ligand milk fat globule–associated protein with epidermal growth factor– and factor VIII–like domains (MFG‐E8) negatively regulates fibrosis in the liver, lungs, and respiratory tract. However, the mechanisms and roles of MFG‐E8 in skin fibrosis in systemic sclerosis (SSc) have not been characterized. We undertook this study to elucidate the role of MFG‐E8 in skin fibrosis in SSc. Methods We assessed expression of MFG‐E8 in the skin and serum in SSc patients. We examined the effect of recombinant MFG‐E8 (rMFG‐E8) on latent transforming growth factor β (TGFβ)–induced gene/protein expression in SSc fibroblasts. We examined the effects of deficiency or administration of MFG‐E8 on fibrosis mouse models. Results We demonstrated that MFG‐E8 expression around dermal blood vessels and the serum MFG‐E8 level in SSc patients (n = 7 and n = 44, respectively) were lower than those in healthy individuals (n = 6 and n = 28, respectively). Treatment with rMFG‐E8 significantly inhibited latent TGFβ–induced expression of type I collagen, α‐smooth muscle actin, and CCN2 in SSc fibroblasts (n = 3–8), which suggested that MFG‐E8 inhibited activation of latent TGFβ as well as TGFβ signaling via binding to αv integrin. In a mouse model of bleomycin‐induced fibrosis (n = 5–8) and in a TSK mouse model (a genetic model of SSc) (n = 5–10), deficient expression of MFG‐E8 significantly enhanced both pulmonary and skin fibrosis, and administration of rMFG‐E8 significantly inhibited bleomycin‐induced dermal fibrosis. Conclusion These results suggest that vasculopathy‐induced dysfunction of pericytes and endothelial cells, the main cells secreting MFG‐E8, may be associated with the decreased expression of MFG‐E8 in SSc and that the deficient inhibitory regulation of latent TGFβ–induced skin fibrosis by MFG‐E8 may be involved in the pathogenesis of SSc and may be a therapeutic target for fibrosis in SSc patients.
    Type of Medium: Online Resource
    ISSN: 2326-5191 , 2326-5205
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2754614-7
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  • 2
    In: Arthritis & Rheumatology, Wiley, Vol. 70, No. 10 ( 2018-10), p. 1661-1672
    Abstract: Apelin/ APJ signaling has been determined to regulate cardiac and arterial fibrosis and to be involved in the pathogenesis of pulmonary arterial hypertension. Our objective was to elucidate the role of apelin in skin fibrosis in systemic sclerosis ( SS c). Methods Expression of apelin/ APJ in normal and SS c fibroblasts was compared. Effects of small interfering RNA depletion and the addition of apelin in fibroblasts were analyzed. The effect of apelin injections on bleomycin‐induced dermal fibrosis in mice was investigated. We analyzed the effects of the biased agonist of APJ , MM 07, on skin fibrosis in vitro and in vivo. Results The expression of apelin in SS c fibroblasts was significantly lower than that in normal fibroblasts. Serum apelin levels were negatively correlated with the modified Rodnan skin thickness score in SS c patients. Stimulation with transforming growth factor β1 ( TGF β1) inhibited apelin expression in fibroblasts, suggesting that activation of TGF β1 signaling in SS c might be responsible for reduced apelin expression in SS c fibroblasts. Small interfering RNA depletion of apelin from fibroblasts significantly enhanced fibrosis‐related gene expression, and treatment with apelin protein significantly inhibited TGF β1 signaling in fibroblasts. Administration of apelin significantly inhibited bleomycin‐induced dermal fibrosis in mice. We demonstrated that MM 07 had greater potential than apelin to inhibit fibrosis in vivo and in vitro. Conclusion Collectively, TGF β1 signaling and apelin signaling may counteract each other in the fibrotic process of SS c. Inhibitory regulation of TGF β1‐induced skin fibrosis by apelin/ APJ signaling may be involved in the pathogenesis of SS c and could be a therapeutic target for fibrosis in SS c patients.
    Type of Medium: Online Resource
    ISSN: 2326-5191 , 2326-5205
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2018
    detail.hit.zdb_id: 2754614-7
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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