Comparison of Antiobesity Effects of Adipose-Derived Stromal/Stem Cells from Different Sources in a Natural Aging Model.

PURPOSE: Our previous study found that white adipose stem cells (W-ASCs) derived from abdominal and femoral sulcus white adipose stem cells (ASCs) have antiaging and age-related obesity effects. Whether interscapular brown adipose stem cells (B-ASCs) have the same effect has not been reported. The study objective was to compare the effects of ASCs from different tissues on aging and aging-related obesity. PATIENTS AND METHODS: C57BL/6J mice at 22 months of age were transplanted with either B-ASCs or W-ASCs from young mice at 2 months of age. Changes in body weight, biochemistry, cytokines, hormone secretion, cell senescence, lipid metabolism, and ASC function were assessed after transplanted 1 month.
RESULTS: W-ASCs were superior to B-ASCs as aging and age-related obesity indicators, based on change in body weight, organ weight, antioxidant and anti-inflammatory activity, lipid metabolism, and liver and kidney function.
CONCLUSION: Difference in the tissue source was reflected by the heterogeneity of antiaging and age-related obesity effects of transplanted ASCs. Based on the study results, we recommend W-ASCs over B-ASCs in aging and age-related obesity applications.

Introduction

Obesity is a problem from birth throughout aging. Increased visceral fat is one of the changes that accompanies aging, and changes in the abundance and distribution of adipose tissue, and in endocrine signals with aging can have negative outcomes, such as chronic inflammation and chronic diseases including type 2 diabetes.1,2 Regardless of such developments, research on how aging and obesity interact is incomplete.

The two forms of mammalian fat are white adipose tissue (WAT) and brown adipose tissue (BAT).3 WAT stores excess energy as triglycerides (TGs) to maintain energy metabolism.4 BAT consumes energy and releases it as heat. BAT cells are small and contain many mitochondria; and, in experimental animal studies, BAT has been found to inhibit the development of obesity.3–5 Adipose stem cells (ASCs) are easily obtained from adult adipose tissue, have high proliferative activity, and ability to differentiate is second only to embryonic stem cells.6 The primary role of ASCs is to maintain adipocyte homeostasis by self-renewal and differentiation. In addition, it is also related to immunity and metabolism.7,8

The correlation between aging and obesity is obvious, and ASCs are closely related to obesity. To investigate the role of ASCs in aging and obesity, we followed the changes in adipose stem cells isolated from WAT and BAT that occurred in a mouse model of aging The results indicated that the content of WAT was increased in old mice and the content of BAT was increased in young mice. The numbers of senescent cells and the rate of apoptosis of ASCs were significantly higher in old compared with young mice, and osteogenic and adipogenic differentiation capacity were decreased.9

Previous studies have reported the osteogenic differentiation of ASCs in young mice9,10 and that the intravenous injection of fat-derived stem cells with autologous ASCs effectively regulated the blood and biochemical parameters, renal function, and antioxidant enzyme activity of elderly rats.10 In this study, intraperitoneal injection of white adipose stem cells (W-ASCs) in young mice reduced the gain in body weight observed in old mice, increased the levels of antioxidant enzymes such as superoxide dismutase (SOD) and catalase (CAT), and decreased the levels of inflammatory factors such as tumor necrosis factor (TNF-α) and interleukin-6 (IL-6).11 The study objectives were to determine whether, as an energy-consuming and heat-producing tissue, brown fat stem cells (B-ASCs) could antagonize age-related obesity and improve age-related obesity, and what the differences exist between them and W-ASCs.

Materials and Methods

Animal Preparation and Transplantation

C57BL/6J mice were obtained from the Department of Experimental Animal Stem Cells of Guangxi Normal University (Guilin, China). The study procedures approved by, and followed the Guidelines of, the Animal Care and Use Committee of Guangxi Normal University. The animals were raised under specific pathogen-free conditions and all were maintained with a 12-hour light/dark cycle at 23 ± 2°C, and free access to water and a standardized 10% lipid diet. The young and old mouse models were established as previously described.11 The young mice were 2 months of age; the old mice were 22 months of age. W-ASCs and B-ASCs were obtained from young mice. Thirty old mice were randomly assigned to three groups of ten each, with intraperitoneal injection of 106 W-ASCs or B-ASCs in the experimental groups and phosphate buffer solution (Sangon Biotech, E607008) in the control group, and the time of transplantation was 1 month.

Isolation and Culture of W-ASCs and B-ASCs

The isolation and culture of W-ASCs and B-ASCs have been previously described.9 The mice were anesthetized, and WAT was removed from the groin and BAT from the scapula with sterile surgical scissors and forceps after washing with phosphate buffered saline. After digestion, DMEM/F12 (Fisher Scientific, 8,115,296) medium containing 10% fetal bovine serum (Fisher Scientific, 1,715,752) was added, after the tissue was passed through a 70 μm screen (BD Bioscience), the cells were centrifuged at 300 g for 5 min and the supernatant was discarded. The cells were washed twice with DMEM/F12 and centrifuged again at 300 g for 5 min. The supernatant was discarded, and the resulting matrix and vascular components were resuspended in DMEM/F12 medium containing 10% fetal bovine serum in cell-culture plates. The culture medium was changed after 36–48 hours, and the ASCs that had adhered to the plastic surface were cultured to 80% confluence. We examined the immunophenotyping (CD29+/CD44+/CD105+/CD45–) of ASCs by flow cytometry, and Antibodies were from Thermo Fisher (). The third generation of cells was used in the experimental procedures.

Proliferation and Differentiation of ASCs

The methods used to assay ASC proliferation and differentiation have been previously described.11 ASC proliferation was assayed with a methylthiazol tetrazolium (MTT) method and colony formation. ASC osteogenic and adipogenic differentiation were induced by culture in adipogenic and osteogenic media. Oil red (Solarbio, G1262) and alizarin (Solarbio, G8550 red were used to detect the formation of lipid droplets and calcium.

Assay of Cellular Senescence

ASCs from the transplantation and control groups were cultured for three generations and transferred at 10,000 cells/well to 96-well plates. After 24 hours of culture, the cells that had adhered to the culture wells were fixed with paraformaldehyde and then stained following the manufacturer’s (Sigma, CS0030MSDS) instructions. The senescent cells were counted cells and reported as a percentage of the total cell population.

Serum Biochemical and Mitochondrial Assays

Serum biochemistry and mitochondrial membrane potential were assayed as previously described.11 Whole blood was collected from the eyelid and centrifuged at 12,000 rpm at 4°C for 15 min. The serum was collected and stored at −80°C. Serum TG, total cholesterol, high-density lipid (HDL) cholesterol, low-density lipid (LDL) cholesterol, glucose (GLU), blood urea nitrogen (BUN), glutamic acid transaminase (ALT), glutamic acid transaminase (AST) and creatinine (CREA) were determined with an autoanalyzer (HITACHI-720). Serum SOD, catalase (CAT), sex hormone-binding globulin (SHBG), and thyroid stimulating hormone (TSH) were determined with enzyme-linked immunosorbent assay kits (R & D Systems). Mitochondrial membrane potential was measured with a mitochondrial dark red fluorescent probe following the manufacturer’s instructions (Yeasen, 40743ES50).

Tissue Weight and Histology

After collecting blood, abdominal adipose tissue, liver, kidney, and spleen were removed and weighed. Liver tissue was fixed in neutral buffered formalin, processed, embedded in paraffin, sectioned, and stained with hematoxylin and eosin (Solarbio, G1120) or Oil Red O (Solarbio, G1262). Light microscopy and ImageJ version 5.0 software were used to measure the size of adipocytes and stored lipid droplets.11

Cytokine Analysis

A Luminex system (Millipore, Burlington, MA, USA) and mouse cytokine kits were used to assay tumor necrosis factor (TNF)-α, interleukin (IL)-1β, IL-6, chemokine ligand 2 (CCL2), C-X-C motif chemokine ligand 12 (CXCL12), epidermal growth factor (EGF), vascular endothelial growth factor (VEGF), fibroblast growth factor (FGF), and leptin (LEP). The samples were assayed in duplicate.7

Labeled ASCs

ASCs were labeled with 4ʹ, 6-diamidine-2-phenyl indole (DAPI) and observed by blue fluorescence microscopy. Labeled cells were then transplanted into aging mice by intraperitoneal injection. Seven days later, abdominal fat was removed, embedded in optimal cutting temperature compound, and frozen sections were observed by light microscopy.

Statistical Analysis

Results were reported as means and standard deviation and P-values < 0.05 was considered statistically significant. Data were analyzed using GraphPad Prism 9.0 for t- tests or two-way analysis of variance.

Results

Changes in Body Weight, Visceral Fat Weight, Abdominal Fat Weight, and ASC Homing

Body fat, especially visceral fat, increases during aging.12,13 B-ASCs and W-ASCs from young mice were transplanted into naturally aging mice. The same volume of phosphate buffered saline was transplanted into the control group. The weight changes of that occurred in the aging mice within 4 weeks after injection are shown in (Figure 1A). The weight of mice transplanted with ASCs decreased in the first 2 weeks; the weight of mice in the control group increased. The weight of mice in the transplant groups increased in the last 2 weeks, but the rate of weight gain was lower than that of the control group. After 4 weeks, the mean weight in the W-ASC transplantation group (25.2 ± 0.6 g) was 18.7% less than that of the control group (31.0 ± 1.0 g). The mean weight in the B-ASC transplantation group (27.4 ± 0.4 g) was 11.5% lower that of the control group. There were no differences in food intake between the control group and the transplantation groups (Figure 1B).

Figure 1

Weight-related changes and transplantation of labeled B-ASCs and W-ASCs. (A) Body weight. (B) Daily food intake. (C) Labeled ASCs (100×). (D) Visceral fat weight. (E) Abdominal fat weight. Data are from four independent experiments (n = 10) and reported as means ± standard deviation. Statistical analysis was conducted with GraphPad Prism 9 software.**P < 0.01; ****P < 0.0001.

To explain the changes that occurred, we observed the DAPI-labeled ASCs 7 days after transplantation of into aging mice in frozen sections of abdominal fat (Figure 1C). We also weighed the internal organs and abdominal fat in each group (Figure 1D and E). Compared with the control group (0.26 ± 0.24 g), the weight of the spleen in the aging mice had decreased by 50.00% after B-ASC transplantation (0.13 ± 0.3 g) and by 69.2% after W-ASC transplantation. Transplantation of B-ASCs had no significant effects on the weight of the kidneys or livers of naturally aging mice. The kidney weight decreased by 43.86% and the liver weight decreased by 33.91% (P < 0.001) after W-ASC transplantation compared with the control group. Compared with the control group, the weight of the abdominal fat weight was reduced by 28.95% after transplantation of B-ASCs and by 52.63% after transplantation of W-ASCs (P < 0.01).

Effects of B-ASCs and W-ASCs on Lipid Metabolism

To investigate the effects of ASC transplantation on lipid metabolism during aging, we measured the size of the lipid droplets in abdominal fat, mitochondrial activity, and serum lipid levels. Hematoxylin and eosin staining of paraffin-embedded sections of abdominal fat showed that the diameter of fat droplets in adipose cells was significantly smaller in aging mice after B-ASC and W-ASC transplantation than in the control group (Figure 2A). The fat droplet area was measured by Image J (Figure 2B); the differences significant (P < 0.05 for B-ASCs and P < 0.001 for W-ASCs). Both B-ASC and W-ASC transplantation significantly increased the TG level of aging mice (P < 0.05), and decreased GLU and HDL cholesterol (both P < 0.0001). There was no significant effect on total cholesterol and LDL cholesterol (Figure 2C). There was thus no overall difference in the effects of B-ASC and W-ASC transplantation on the blood lipid levels of naturally aging mice. ASC transplantation enhanced mitochondrial activity, and the effect of B-ASC transplantation was stronger than that of W-ASCs (Figure 2D).

Figure 2

Effect of B-ASC and W-ASC transplantation on lipid metabolism. (A) Hematoxylin and eosin staining of paraffin-embedded abdominal adipose tissue. (B) The size of fat droplets in abdominal adipose tissue. (C) Blood lipid levels. (D) Mitochondrial activity in abdominal adipocytes. Data are from four independent experiments (n = 5) and reported as means ± standard deviation. Statistical analysis was conducted with GraphPad Prism 9 software. *P < 0.05; ***P < 0.001.

Effects of B-ASC and W-ASC Transplantation on Aging Markers

The effects of ASC transplantation were evaluated by age-related oxidative stress, enzyme activity, and cellular senescence. Compared with the control group, SOD and CAT levels were increased by B-ASC and W-ASC transplantation. The differences in SOD level were significant for both types of ASCs (P < 0.001), but the difference in CAT levels was significant for only W-ASCs (P < 0.01). Sex hormone-binding globulin (SHBG) and TSH were both increased by ASC transplantation, but the difference was significant only for W-ASCs (P < 0.01 and P < 0.05, respectively, Figure 3A). The β-galactosidase cell counts in the B-ASC (P < 0.01) and the W-ASC (P < 0.001) transplantation groups were significantly lower than the count in the control group (Figure 3B). In general, ASC transplantation reversed some of the aging criteria, and the W-ASCs had a greater effect than the B-ASCs.

Figure 3

Antiaging effects of B-ASC and W-ASC transplantation. (A) Serum levels of superoxide dismutase (SOD), catalase (CAT), sex hormone-binding globulin (SHBG), and thyroid stimulating hormone (TSH). (B) Senescence-associated beta-galactosidase staining of ASCs from all study groups. Data are from four independent experiments (n = 7) and reported as means ± standard deviation. Statistical analysis was conducted with GraphPad Prism 9 software. *P < 0.05; **P < 0.01; ***P < 0.001.

Effects of B-ASC and W-ASC Transplantation on Serum Cytokines

Aging is usually accompanied by chronic systemic inflammation.14 The influence of ASCs on the extent of inflammation in naturally aging mice was evaluated by the levels of some serum cytokines (Figure 4). Compared with the control group, TNF-α was 48.41% lower in B-ASC transplantation group and 52.64% in the W-ASC group (P < 0.05). The corresponding differences in IL-6 level were 62.83% and 84.86%, respectively, but neither were significant. LEP was significantly increased in the W-ASC group (P < 0.001) and VEGF was significantly decreased (P < 0.05) compared with the control group. The differences in LEP and VEGF levels between the B-ASC group and the control group were not significant. Differences between IL-1β, CCL12, CXCL12, EGF, and FGF in the control and ASC transplantation groups were not significant.

Figure 4

Serum cytokine concentrations. Data are mean ± standard deviation (n = 8). Statistical analysis was conducted with GraphPad Prism 9. *P < 0.05; ***P < 0.001.

Effects of B-ASCs and W-ASCs on the Plasticity of Abdominal ASCs in Naturally Aging Mice

The relationships between abdominal fat loss and changes in abdominal-ASC function were investigated in ASCs isolated from abdominal fat. ASC proliferation was evaluated by an MTT assay and colony formation. The results (Figure 5A and B) showed that there were no differences between the control and the transplantation groups. The effects on osteogenic and adipogenic differentiation are shown in Figure 5C and D. W-ASCs significantly enhanced osteogenic differentiation of abdominal ASCs (P < 0.05); the effect of B-ASCs was not significant. Compared with the control group, both B-ASCs and W-ASCs significantly reduced adipogenic differentiation by abdominal ASCs in naturally aging mice (P < 0.01 and P < 0.001, respectively).

Figure 5

Effects of B-ASC and W-ASC transplantation on the plasticity of abdominal ASCs. (A) MTT assay of cell proliferation. (B) Colony count. (C) Osteogenic differentiation. (D) Adipogenic differentiation. Data are means ± standard deviation (n = 5). Statistical analysis was conducted with GraphPad Prism 9. *P < 0.05; **P < 0.01; and ***P < 0.001.

Effects of B-ASCs and W-ASCs on Liver and Kidney Function of Naturally Aging Mice

The effects of ASC transplantation on liver function were evaluated by ALT and AST levels (Figure 6A). Compared with the control group, ALT decreased in both transplantation groups, but the differences were not significant The reduction in AST was significant in both the B-ASC (P < 0.001) and W-ASC groups (P < 0.01). The effects of ASC transplantation on renal function were measured by CREA and BUN levels (Figure 6B). Compared with the control group, CREA was significantly reduced in both the B-ASC (P < 0.05) and the W-ASC (P < 0.001) groups; the differences in BUN levels were not significant. Liver lipid accumulation was evaluated by histological staining (Figure 6C and D). Accumulation of lipid and lipid droplets was significantly reduced in both transplantation groups. The results indicate that ASC transplantation did not damage liver and kidney function, and improved liver and kidney function of aging mice to a certain extent.

Figure 6

Effects of B-ASC and W-ASC transplantation on liver and kidney function. (A) ALT and AST levels. (B) CREA and BUN levels. (C) Liver tissue, hematoxylin and eosin staining of paraffin sections. (D) Frozen sections of liver tissue, Oil Red O staining. Data are means ± standard deviation (n = 5). Statistical analysis was conducted with GraphPad Prism 9. *P < 0.05; **P < 0.01; and ***P < 0.001.

Discussion

Our previous studies found that ASCs derived from inguinal white fat had the effect of resisting age-related obesity and improved age-related characteristics.11 The evidence supported the potential effectiveness of ASC transplantation for the treatment of aging and aging-related obesity. However, cells isolated from different sources and in different physiological states are likely to produce different therapeutic effects.15,16 Previous studies have shown that CRISPR-engineered human brown fat cells were able to prevent diet-induced obesity and improve metabolic syndrome in mice,17 but the effect of B-ASCs on aging and age-related obesity is not clear. Therefore, we compared the effects of inguinal W-ASCs from scapular B- ASCs from the scapula in the treatment of aging and age-related obesity. Both B-ASCs and W-ASCs had an effect on the reversal of age-related obesity and improvement of age-related characteristics, but the overall effects of B-ASCs were not as good as those of W-ASCs.

Both B-ASCs and W-ASCs reversed the increase in body weight of aging mice, which may be explained by decreases in abdominal fat content and abdominal organ weight. B-ASCs and W-ASCs reduced the abdominal fat weight of aging mice, and W-ASC but not B-ASC transplantation significantly reduced the spleen and liver weights. The difference might have been related to differences in the reduction of inflammation mediated by B-ASCs and W-ASCs. The weight of both the spleen and liver increase with age,18–20 and B-ASCs had less of an effect on age-related inflammation than that W-ASCs did. The serum cytokine results were consistent with the effects on inflammation, but the reasons need further investigation. We confirmed that the observed changes were not caused by differences in the amount of food intake; there were no differences in food intake among the groups. In addition, labeled B-ASCs and W-ASCs were found in abdominal fat tissue, which shows that the homing of transplanted ASCs to abdominal fat tissue played a role; reduction of abdominal fat weight and differentiation of abdominal ASCs also reflects this point.

Increased oxidative stress is an aging characteristic of aging, and oxidative damage accelerates the occurrence of some age-related diseases. High levels of oxidative stress can also accelerate the aging of mesenchymal stem cells and reduce their ability to differentiate into osteoblastic cells.21,22 B-ASC and W-ASC transplantation reduced oxidative stress in aging mice, which also explained the increase in the number of abdominal ASCs with aging and osteogenic differentiation capacity in the transplantation groups, but the improvement in oxidative stress in aging mice was less with B-ASCs than with W-ASCs. Decreases of SHBG and TSH also occur during aging, and decreases may aggravate age-related diseases.23,24 B-ASC and W-ASC transplantation were both followed by increases levels of TSH and SHBG, but the increase associated with B-ASCs was smaller than that following W-ASC transplantation. Both B-ASCs and W-ASCs significantly reduced blood glucose levels in aging mice, which may have been related to enhanced mitochondrial activity in adipose tissue and reduced insulin resistance.25 LEP levels were significantly increased by W-ASC but not by B-ASCs, suggesting changes in TSH because leptin and TSH are correlated.26

Our study found that B-ASCs and W-ASCs have antiaging and antiobesity effects, and that transplantation of B-ASCs and W-ASCs did not cause liver or kidney damage in the aging mice. Liver and kidney function were improved to a certain extent, which is consistent with other studies.27 Briefly, ASC isolated from different tissues had heterogeneous antiaging and antiobesity effects, but the causes of such differences are not clear. Theoretically, because of brown fat thermogenesis, ASCs derived from brown fat would have better antiobesity effects, but we did not observe that. The superior antiaging and obesity-resistance effects of W-ASCs may have resulted from their anti-inflammatory and antioxidant effects, and their effects on hormone secretion, but data to support that view are lacking.

Conclusion

This study compared the effects of ASCs derived from white and brown adipose tissue on aging and age-related obesity in a mouse model. The effect of inguinal W-ASCs on body weight, age-related changes in enzymes, hormones, and inflammatory factors was better than that of scapular B-ASCs. Differences in the tissue of origin were reflected by the heterogeneity of the responses to ASCs in aging and age-related obesity. The study provides a theoretical basis for the future clinical use of ASCs in aging and aging-related obesity.