Skip to main content
. Author manuscript; available in PMC: 2014 Oct 5.
Published in final edited form as: Cell Metab. 2013 Sep 3;18(3):355–367. doi: 10.1016/j.cmet.2013.08.003

Figure 7. PDGFRα+ Cells Interact with Macrophages in Adult WAT and Contribute to Adipogenesis during Tissue Repair, Tissue Neogenesis, and Nutritional Hyperplasia.

Figure 7

(A) 3D projection images of CLS in iWAT whole mounts from Pdgfra-CreERT2/tdTomato mice fed HFD for 8 weeks.

(B) tdTomato+ adipocyte clusters that were found in iWAT of HFD-fed mice were not associated with CLS.

(C and D) Needle injury induced the appearance of tdTomato+ adipocyte clusters in iWAT. Shown are cryosections of Pdgfra-CreERT2/tdTomato mice 10 days after needle injury. (D) A magnified view of the boxed region from (C). Injured sites were marked with DiO (green, left). tdTomato+ multilocular adipocytes (arrows) contained PLIN1+ lipid droplets.

(E and F) Representative confocal images of Matrigel plugs 7 days or 4 weeks after injection. (E) tdTomato+ progenitors and F4/80+ macrophages were the major cells infiltrating Matrigel plugs 7 days after injection. (F) Numerous tdTomato+ adipocytes formed 4 weeks after Matrigel injection.

(G) Heatmap showing the unique gene expression profiles of macrophage-associated genes under different adipogenic conditions. Gene expression values are relative to each control condition. (n = 4–6; bold, p < 0.05).

(H) PCA score plot illustrates distinct gene expression profiles across adipogenic conditions (CLd3, gWAT of mice treated with CL for 3 days; injury, iWAT of mice 3 days after needle injury; HFD, gWAT of mice fed HFD for 8 weeks; neogenesis, Matrigel plug 7 days after injection). Scale bars, 20 µm in (A), (B), and (D). Scale bars, 100 µm in (C), (E), and (F). See also Figure S7.