Microcurrent Reverses Cigarette Smoke-Induced Angiogenesis Impairment in Human Keratinocytes In Vitro.
Chao LuCosima PrahmYangmengfan ChenSabrina EhnertHelen RinderknechtColin D McCaigAndreas K NusslerJonas KolbenschlagPublished in: Bioengineering (Basel, Switzerland) (2022)
Cigarette smoking (CS) leads to several adverse health effects, including diseases, disabilities, and even death. Post-operative and trauma patients who smoke have an increased risk for complications, such as delayed bone or wound healing. In clinical trials, microcurrent (MC) has been shown to be a safe, non-invasive, and effective way to accelerate wound healing. Our study aimed to investigate if MC with the strength of 100 μA may be beneficial in treating CS-related healing impairment, especially in regard to angiogenesis. In this study, we investigated the effect of human keratinocyte cells (HaCaT) on angiogenesis after 72 h of cigarette smoke extract (CSE) exposure in the presence or absence of 100 μA MC. Cell viability and proliferation were evaluated by resazurin conversion, Sulforhodamine B, and Calcein-AM/Hoechst 33342 staining; the pro-angiogenic potential of HaCaT cells was evaluated by tube formation assay and angiogenesis array assay; signaling pathway alterations were investigated using Western blot. Constant exposure for 72 h to a 100 μA MC enhanced the angiogenic ability of HaCaT cells, which was mediated through the PI3K-Akt signaling pathway. In conclusion, the current data indicate that 100 μA MC may support wound healing in smoking patients by enhancing angiogenesis.
Keyphrases
- wound healing
- endothelial cells
- induced apoptosis
- signaling pathway
- high glucose
- cell cycle arrest
- vascular endothelial growth factor
- clinical trial
- endoplasmic reticulum stress
- oxidative stress
- end stage renal disease
- high throughput
- epithelial mesenchymal transition
- chronic kidney disease
- cell death
- newly diagnosed
- mass spectrometry
- peritoneal dialysis
- emergency department
- machine learning
- prognostic factors
- bone mineral density
- cell proliferation
- pluripotent stem cells
- soft tissue