2022
DOI: 10.1016/j.biopha.2022.113143
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Insight into the role of DPP-4 in fibrotic wound healing

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Cited by 19 publications
(16 citation statements)
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“…In the subcapsular zone we characterize important roles of specialized fibroblast cells, where DPP4 + capsular fibroblasts respond to systemic hormone levels and capsular fibroblasts contribute to DP development indirectly through maintenance of cortical epithelial cells, as well as directly through immunoregulatory growth factors. DPP4 + capsular fibroblasts have been described in mouse in the thymic capsule 83 and elsewhere as cells with progenitor and anti-fibrotic potential [84][85][86][87] . Here, we observe that DPP4 marks a subset of capsule fibroblasts which can respond to changes in systemic hormone levels.…”
Section: Discussionmentioning
confidence: 99%
“…In the subcapsular zone we characterize important roles of specialized fibroblast cells, where DPP4 + capsular fibroblasts respond to systemic hormone levels and capsular fibroblasts contribute to DP development indirectly through maintenance of cortical epithelial cells, as well as directly through immunoregulatory growth factors. DPP4 + capsular fibroblasts have been described in mouse in the thymic capsule 83 and elsewhere as cells with progenitor and anti-fibrotic potential [84][85][86][87] . Here, we observe that DPP4 marks a subset of capsule fibroblasts which can respond to changes in systemic hormone levels.…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, increased DPP-IV levels are observed in obese patients and correlate with a higher risk for the development of metabolic complications [ 63 ]. Moreover, increased DPP-IV could also provide a link with the fibrotic states detected in aged NRK1 KO mice, as DPP-IV can trigger multiple processes leading to fibrotic extracellular matrix depositions [ 64 , 65 ]. Oppositely, the inhibition of DPP-IV has been shown to attenuate fibrosis in liver [ 65 , 66 ] and kidney [ [67] , [68] , [69] ].…”
Section: Discussionmentioning
confidence: 99%
“…82,86 Although in Taiwan, DPP-4 inhibitors (DPP-4i) effect on the bone health in T2DM patients seemed to be supported by largescale population-based study as shown by Dr. Chang's group, 56 and additionally, DPP-4 has been extensively reviewed to provide the possible benefits on bone and subcutaneous tissue (extracelluar matrix), which are key factors of bone health. 89,90 Similar to many large-scale population-based studies, 31,56,63,[83][84][85][86][91][92][93][94][95][96][97][98] many biases, which cannot be totally excluded, may decrease the reliability and reproducibility of the data analysis. Additionally, DPP-4i may increase the risk of cholecystitis in randomized controlled trials, especially with longer treatment duration, 99 although the population-based cohort study did not support the current use of DPP-4i was associated with an increased risk of bile duct and gallbladder disease compared with current use of at least 2 oral ADA (adjusted HR, 0.99; 95% CI, 0.75-1.32).…”
Section: Antidiabetic Agents and Bonementioning
confidence: 99%