» Articles » PMID: 26323987

Bone Marrow Mesenchymal Stem Cell Implantation for the Treatment of Radioactivity‑induced Acute Skin Damage in Rats

Overview
Journal Mol Med Rep
Specialty Molecular Biology
Date 2015 Sep 2
PMID 26323987
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

The present study aimed to observe the role of mesenchymal stem cells (MSCs) in the repair of acute skin damage caused by radiation. Rat bone marrow MSCs (BMSCs) were isolated and cultured in vitro. A rat model of radiation‑induced acute skin damage was established by irradiation of the hind legs of Sprague-Dawley rats using a linear accelerator (45 Gy). After irradiation, rats were randomly divided into two groups: BMSC group and control group. Rats in the BMSC group were treated with a tail vein injection of 2x106 BMSCs (1 ml) immediately after irradiation and a local multipoint injection of 2x106 BMSCs at the injured area two weeks later. Then the wound healing of each rat was observed. The expression of transforming growth factor (TGF)‑β1, stromal cell‑derived factor-1 (SDF‑1) and prostaglandin E2 (PGE2) in the wounded tissues was determined by immunohistochemistry. The results demonstrated that skin damage was milder in the BMSC group than in the control group. Moreover, the speed of healing in the BMSC group was better than that in the control group. In addition, the wound score, it was significantly lower in the BMSC group than in the control group (P<0.05). The expression of PGE2 and TGF‑β1 in the BMSC group was also significantly lower than that in the control group (P<0.05), whereas the SDF‑1 expression was significantly higher in the BMSC group than that in the control group (P<0.05). BMSCs can effectively reduce inflammation and fibrosis in the wounded skin and promote the repair of acute radioactive skin injury. Thus, may be developed as a novel treatment for wound healing.

Citing Articles

Evaluation of the Effects of Radiation Therapy on Muscle Contractibility and Skin Healing: An Experimental Study of the Cancer Treatment Implications.

Avelino S, Neves R, Sobral-Silva L, Tango R, Federico C, Vegian M Life (Basel). 2023; 13(9).

PMID: 37763242 PMC: 10532574. DOI: 10.3390/life13091838.


Revolutionizing Radiotoxicity Management with Mesenchymal Stem Cells and Their Derivatives: A Focus on Radiation-Induced Cystitis.

Helissey C, Cavallero S, Guitard N, Thery H, Chargari C, Francois S Int J Mol Sci. 2023; 24(10).

PMID: 37240415 PMC: 10219063. DOI: 10.3390/ijms24109068.


Human Mesenchymal Stromal Cells Do Not Cause Radioprotection of Head-and-Neck Squamous Cell Carcinoma.

Ruhle A, Lies M, Strack M, Lopez Perez R, Bieber B, Thomsen A Int J Mol Sci. 2022; 23(14).

PMID: 35887032 PMC: 9323822. DOI: 10.3390/ijms23147689.


Mesenchymal Stem Cells and their Derived Exosomes Promote Malignant Phenotype of Polyploid Non-Small-Cell Lung Cancer Cells through AMPK Signaling Pathway.

Wang L, Ouyang M, Xing S, Zhao S, Liu S, Sun L Anal Cell Pathol (Amst). 2022; 2022:8708202.

PMID: 35419253 PMC: 9001126. DOI: 10.1155/2022/8708202.


Will mesenchymal stem cells be future directions for treating radiation-induced skin injury?.

Fang Z, Chen P, Tang S, Chen A, Zhang C, Peng G Stem Cell Res Ther. 2021; 12(1):179.

PMID: 33712078 PMC: 7952822. DOI: 10.1186/s13287-021-02261-5.