Changes in biological characteristics of adipose-derived stem cells from obese patients post successful weight loss

Wei Zhiru; Dong Yan; Qiao Gaihong; Liu Linbo; Li Guangshuai

doi:10.3760/cma.j.cn501225-20231205-00225

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Article Navigation > CHINESE JOURNAL OF BURNS AND WOUNDS > > Accepted Manuscript

Wei Zhiru, Dong Yan, Qiao Gaihong, et al. Changes in biological characteristics of adipose-derived stem cells from obese patients post successful weight loss[J]. Chin J Burns Wounds. Doi: 10.3760/cma.j.cn501225-20231205-00225

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Changes in biological characteristics of adipose-derived stem cells from obese patients post successful weight loss

doi: 10.3760/cma.j.cn501225-20231205-00225

1.
Department of Plastic Surgery, the First Affiliated Hospital of Zhengzhou University, Zhengzhou450052, China
2.
Department of General, Visceral, and Transplantation Surgery, Heidelberg University Medical School, Heidelberg69120, Germany

Funds:

Science and Technology Development Plan Program of Henan Province of China in 2022 222102310188

More Information

Corresponding author: Li Guangshuai, Email: liguangshuai@zzu.edu.cn
Received Date: 2023-12-05
Available Online: 2024-10-28

Abstract

Abstract

Objective To explore the changes in biological characteristics of adipose-derived stem cells (ASCs) from obese patients post successful weight loss, so as to provide a reference for the clinical application of these ASCs in the repair of refractory wounds. Methods This study was an experimental study. Twelve obese patients (8 females and 4 males, aged (50±9) years) who successfully lost weight, underwent abdominal skin tightening surgery, and were hospitalized at the First Affiliated Hospital of Zhengzhou University from April 2021 to April 2023 were included in weight loss group. During the same period, 12 healthy volunteers (10 females and 2 males, aged (50±9) years) who underwent abdominal liposuction followed by facial fat grafting in the same institution were recruited into healthy group. Adipose tissue was collected from patients in weight loss group and volunteers in healthy group, and ASCs were extracted. Experiments were conducted using ASCs at passages 4 and 5 in their logarithmic growth phase. Cell proliferation levels were assessed using the methyl thiazolyl tetrazolium assay at 0 (immediately), 24, 48, and 72 hours of culture. The cell scratch test was performed and the cell migration rates at 12 and 24 hours after scratching were calculated. The cell Transwell assay was performed and the number of migration cells at 24 hours after culture was counted. Adipogenic and osteogenic induction assays were carried out, and the adipogenic and osteogenic differentiation levels of cells were detected at 18 and 21 days of culture, respectively. Real-time fluorecence quantitative reverse transcription polymerase chain reaction was employed to measure the mRNA expressions of lipoprotein lipase (LPL), peroxisome proliferator-activated receptor gamma (PPARγ), Runt-related transcription factor 2 (Runx2), osteopontin, alkaline phosphatase (ALP), matrix metalloproteinase 9 (MMP-9), and transforming growth factor beta (TGF-β). The sample number of each experiment was 12. Results At 0 hour of culture, the cell proliferation levels of patients in weight loss group and volunteers in healthy group were 1.022±0.056 and 1.000±0.144, respectively, with no statistically significant difference between the groups (P>0.05). At 24, 48, and 72 hours of culture, the cell proliferation levels of patients in weight loss group were 1.366±0.030, 1.353±0.012, and 1.390±0.016, respectively, which were significantly lower than 1.755±0.077, 1.737±0.014, and 1.700±0.023 of volunteers in healthy group (with t values of 16.27, 71.35, and 38.56, respectively, P values all <0.05). At 12 and 24 hours after scratching, the cell migration rates of patients in weight loss group were lower than those of volunteers in healthy group, but the differences were not statistically significant (P>0.05). In the cell Transwell assay, after 24 hours of culture, there was no statistically significant difference in the number of migrated cells between patients in weight loss group and volunteers in healthy group (P>0.05). After 18 days of adipogenic induction, the cell adipogenic differentiation level of patients in weight loss group was significantly lower than that of volunteers in healthy group (t=27.81, P<0.05). After 21 days of osteogenic induction, the cell osteogenic differentiation level of patients in weight loss group was significantly lower than that of volunteers in healthy group (t=14.85, P<0.05). Compared with those of volunteers in healthy group, the mRNA expressions of LPL, PPARγ, TGF-β, and Runx2 of patients in weight loss group were significantly reduced (with t values of 59.48, 146.10, 46.10, and 3.13, respectively, P<0.05), while there were no statistically significant changes in the mRNA expressions of osteopontin, ALP, or MMP-9 (P>0.05). Conclusions Compared with healthy volunteers, ASCs from patients who successfully lose weight exhibit significantly diminished proliferative capacity, relatively weakened differentiation potential, and downregulation of some genes corresponding to adipogenic and osteogenic differentiation, which affects the therapeutic efficacy of these ASCs in treating refractory wounds caused by burns, diabetes, or radiation injuries. Therefore, in clinical application, the donor variability of ASCs needs to be considered.
- Obesity,
- Weight loss,
- Cell proliferation,
- Adipose-derived stem cell,
- Osteogenic differentiation,
- Adipogenic differentiation

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