Kim, Ji Eun Lee, Jung Hwa Kim, Soo Hyun Jung, Youngmee 2024-01-19T23:34:16Z 2024-01-19T23:34:16Z 2021-09-03 2018-01 1937-3341 https://pubs.kist.re.kr/handle/201004/121868 The wound healing process requires enough blood to supply nutrients and various growth factors to the wound area. However, chronic wounds such as diabetic skin ulcers have limited regeneration due to a lack of cellular and molecular signals because of a deficient blood flow. Mesenchymal stem cells (MSCs) are known to provide various factors, including growth factors, cytokines, and angiogenic mediators. Although MSCs have great therapeutic potential, their transplantation has many obstacles, including the time required to culture the cells, the invasiveness of the procedure, and limited stem cell sources. In this study, we induced a diabetic 1 model in rats aged 7 weeks by injecting streptozotocin and citrate buffer solution. After confirming that diabetes was induced in the rats, we created critical sized wounds on the dorsal area of the rats and then injected hydrogels. We performed the experiments with four groups (defect model for the control, self-assembled peptides (SAPs), SAP with soluble substance P, and SAP conjugated with substance P) to treat the wound defect. Tissues were harvested at 1, 2, and 3 weeks after injection and examined for the wound closure, histological analysis, quantitative real-time polymerase chain reaction analysis, and quantification of collagen deposits to investigate stem cell recruitment and full recovery of wounds at an accelerated time period. As our results show, the wounds treated with SAP and substance P exhibited significantly accelerated wound closure, enhanced collagen deposition, and increased angiogenesis. Furthermore, we confirmed the ability of SAP with substance P to promote the recruitment and homing of cells by immunofluorescence staining of a MSC marker. In addition, it was observed that substance P remained in the wound area up to 3 weeks after the injection of SAP with substance P. It is believed that the endogenous MSCs mobilized by substance P had therapeutic effects through their proper differentiation and release of paracrine factors into the wound sites. In conclusion, this study shows that SAP with substance P can promote wound healing to enhance skin regeneration without cell transplantation in a diabetic model. English MARY ANN LIEBERT, INC MESENCHYMAL STEM-CELLS GROWTH-FACTORS STROMAL CELLS IN-VITRO DIFFERENTIATION NANOFIBERS OSTEOARTHRITIS PROGRESSION SCAFFOLDS RELEASE Skin Regeneration with Self-Assembled Peptide Hydrogels Conjugated with Substance P in a Diabetic Rat Model Article 10.1089/ten.tea.2016.0517 1 TISSUE ENGINEERING PART A, v.24, no.1-2, pp.21 - 33 TISSUE ENGINEERING PART A 24 1-2 21 33 scie scopus 000419819600003 2-s2.0-85040614169 Cell & Tissue Engineering Cell Biology Engineering, Biomedical Materials Science, Biomaterials Cell Biology Engineering Materials Science Article MESENCHYMAL STEM-CELLS GROWTH-FACTORS STROMAL CELLS IN-VITRO DIFFERENTIATION NANOFIBERS OSTEOARTHRITIS PROGRESSION SCAFFOLDS RELEASE self-assembled peptides substance P wound healing skin regeneration diabetes