Beneficial Effects of Subcutaneous Fat Transplantation on Metabolism

Presentation on theme: "Beneficial Effects of Subcutaneous Fat Transplantation on Metabolism"— Presentation transcript:

1 Beneficial Effects of Subcutaneous Fat Transplantation on Metabolism
Thien T. Tran, Yuji Yamamoto, Stephane Gesta, C. Ronald Kahn  Cell Metabolism  Volume 7, Issue 5, Pages (May 2008) DOI: /j.cmet Copyright © 2008 Elsevier Inc. Terms and Conditions

2 Figure 1 Schematic of Fat Transplantation Groups
Visceral (VIS; epididymal) or subcutaneous (SC; flank) fat from donor mice expressing whole-body green fluorescent protein (GFP) was transplanted into the VIS or SC area of wild-type C57BL/6 host mice. The sham group had surgery in the VIS or SC area, but no fat was transplanted. Cell Metabolism 2008 7, DOI: ( /j.cmet ) Copyright © 2008 Elsevier Inc. Terms and Conditions

3 Figure 2 Body Weight, Body Composition, Energy Expenditure, and Respiratory Quotient after Fat Transplantation (A and B) In cohorts 1 and 2, body weight gain was similar or higher after VIS fat transplantation, lower after SC-SC fat transplantation, and lowest in the SC-VIS group in comparison to the sham group. (C) Fat mass was similar between the sham and VIS transplantation groups, reduced in the SC-SC group, and most reduced in the SC-VIS group. (D) Percent body fat was significantly lower only in the SC-VIS group as compared to the sham group. (E and F) Lean mass (E) and percent lean mass (F) were significantly higher in the SC-VIS group in comparison to the sham group. (G) Total energy expenditure (TEE; data not shown) and TEE divided by lean mass were not significantly different among all sham and transplantation groups during the light and dark cycles. (H and I) Respiratory quotient (RQ) was significantly higher in the SC-VIS group than in the sham group during the light and dark cycles (H) and at almost all 30 min intervals during the 24 hr measurement period (I), indicating a higher proportion of carbohydrate to fat oxidation in the SC-VIS group. All data are presented as mean ± SEM. ∗ denotes statistical significance at p < 0.05. Cell Metabolism 2008 7, DOI: ( /j.cmet ) Copyright © 2008 Elsevier Inc. Terms and Conditions

4 Figure 3 Basal Plasma Levels of Hormones and Substrates, Glucose Tolerance Test, and Insulin Tolerance Test after Fat Transplantations in Cohort 1 (A) Basal plasma glucose and insulin levels were not significantly different among the VIS transplantation and sham groups, were lower in the SC-SC group, and were lowest in the SC-VIS group. Plasma leptin and total adiponectin levels also had a decreasing pattern, with levels being highest in the sham group and significantly lowest in the SC-VIS group. (B) Plasma samples were electrophoresed through nonreducing SDS gels, transferred to membranes, and probed with rabbit anti-mouse adiponectin antibody. Percent of high molecular weight (HMW) adiponectin to total adiponectin (i.e., HMW + medium molecular weight [MMW] + low molecular weight [LMW]) was not significantly different among the groups. (C) Left: after a 2 hr fast for the glucose tolerance test, glucose was administered intraperitoneally. Glucose levels at 120 min were significantly lower only in the SC-VIS group as compared to the sham group. Right: after an overnight fast for the insulin tolerance test, insulin was injected intraperitoneally. No significant difference in blood glucose levels was observed among the groups. All data are presented as mean ± SEM. ∗ denotes statistical significance at p < 0.05. Cell Metabolism 2008 7, DOI: ( /j.cmet ) Copyright © 2008 Elsevier Inc. Terms and Conditions

5 Figure 4 Direct Measures of Insulin Sensitivity by Hyperinsulinemic-Euglycemic Clamp after Fat Transplantation in Cohort 2 (A) Whole-body insulin sensitivity as quantified by glucose infusion rate (GIR) was not significantly different among the sham, VIS-VIS, and SC-SC groups but was significantly higher in the SC-VIS group. (B) Insulin-stimulated [14C]deoxyglucose (14C-DG) uptake was similar between endogenous VIS fat and endogenous SC fat in the sham group. 14C-DG uptake in the fat grafts was not significantly different in the three transplantation groups and had at least the same level of 14C-DG uptake as endogenous fat. (C) 14C-DG uptake into endogenous SC fat of host mice was greater in the SC-SC and SC-VIS groups in comparison to the sham and VIS-VIS groups. (D) 14C-DG uptake into endogenous VIS fat of the sham and transplantation groups was not significantly different. (E) Hepatic glucose production (HGP) in the basal state was not significantly different among the groups, with a trend for the lowest levels in the SC-VIS group in comparison to the sham group. As expected, during the clamp, insulin decreased HGP in the sham and VIS-VIS groups in comparison to their corresponding basal HGP levels and, more importantly, further decreased HGP in the SC-SC and SC-VIS groups. (F) The greatest percent suppression of HGP during the hyperinsulinemic clamp with respect to the basal level was seen in the SC-SC and SC-VIS groups. (G) Glucose uptake in muscle was not significantly different among the groups. All data are presented as mean ± SEM. ∗ denotes statistical significance at p < 0.05. Cell Metabolism 2008 7, DOI: ( /j.cmet ) Copyright © 2008 Elsevier Inc. Terms and Conditions

6 Figure 5 Histology and Inflammatory Markers in Transplanted and Endogenous Fat in Cohort 2 (A) Hematoxylin and eosin (H&E) staining of VIS and SC fat pads was performed in all groups of cohort 2. Transplanted VIS and SC fat pads had normal histology in comparison to endogenous VIS and SC fat pads in the sham group as shown at 400× magnification. (B) Area of adipocytes was measured on the H&E slides with ImageJ software. Transplanting SC fat into the visceral cavity (SC-VIS) significantly decreased the mean area of the adipocytes in comparison to that of the endogenous SC fat in the sham group. (C) Whole mount of a transplanted fat graft expressing GFP viewed under ultraviolet light. Arrows indicate sites of vascularization in the fat graft. (D) Presence of macrophages and inflammatory markers was assessed by quantifying mRNA levels of the macrophage cell surface marker F4/80 (Emr1) and the inflammatory cytokines Il6 and Tnf by real-time qRT-PCR. mRNA levels in VIS-VIS fat grafts were significantly higher than those in endogenous VIS fat in the sham group. There were no significant differences in macrophages, Il6, or Tnf among the SC-SC and SC-VIS fat grafts and the endogenous fat pads. All data are presented as mean ± SEM. ∗ denotes statistical significance at p < 0.05. Cell Metabolism 2008 7, DOI: ( /j.cmet ) Copyright © 2008 Elsevier Inc. Terms and Conditions

7 Figure 6 Gene Expression in Endogenous and Transplanted Fat
Gene expression was measured by real-time qRT-PCR and expressed in terms of mRNA levels relative to Fabp4 (aP2). Analyses of the fat-related molecules Pparg, Fas, leptin, adiponectin, resistin, and Rbp4 show that (1) transplanted VIS-VIS, SC-SC, and SC-VIS fat grafts express Pparg and Fas mRNA levels that are not significantly different from those of endogenous VIS or endogenous SC fats in the sham group; (2) adding more fat of the same depot (VIS-VIS or SC-SC) does not change gene expression levels of the fat genes analyzed, except for resistin and Rbp4 in the VIS-VIS group; and (3) adding SC fat to the VIS cavity (SC-VIS) lowers mRNA levels of leptin, adiponectin, resistin, and Rbp4 in comparison to levels in the endogenous VIS and SC fat depots in the sham group. All data are presented as mean ± SEM. ∗ denotes statistical significance at p < 0.05. Cell Metabolism 2008 7, DOI: ( /j.cmet ) Copyright © 2008 Elsevier Inc. Terms and Conditions