Human Macrophages Preferentially Infiltrate the Superficial Adipose Tissue

Int J Mol Sci. 2018 May 8;19(5):1404. doi: 10.3390/ijms19051404.

Abstract

Human abdominal subcutaneous adipose tissue consists of two individual layers—the superficial adipose tissue (SAT) and deep adipose tissue (DAT)—separated by the Scarpa’s fascia. The present study focuses on the analysis of morphological and immunological differences of primary adipocytes, adipose-derived stem cells (ASC), and tissue-infiltrating immune cells found in SAT and DAT. Adipocytes and stromal vascular fraction (SVF) cells were isolated from human SAT and DAT specimens and phenotypically characterized by in vitro assays. Ex vivo analysis of infiltrating immune cells was performed by flow cytometry. Primary adipocytes from SAT are larger in size but did not significantly differ in cytokine levels of LEPTIN, ADIPOQ, RBP4, CHEMERIN, DEFB1, VISFATIN, MCP1, or MSCF. ASC isolated from SAT proliferated faster and exhibited a higher differentiation potential than those isolated from DAT. Flow cytometry analysis indicated no specific differences in the relative numbers of ASC, epithelial progenitor cells (EPC), or CD3⁺ T-cells, but showed higher numbers of tissue-infiltrating macrophages in SAT compared to DAT. Our findings suggest that ASC isolated from SAT have a higher regenerative potential than DAT-ASC. Moreover, spatial proximity to skin microbiota might promote macrophage infiltration in SAT.

Keywords: adipose-derived stem cells; deep adipose tissue; immune cell infiltration; macrophages; superficial adipose tissue.

MeSH terms

  • Adipocytes / metabolism
  • Adipocytes / pathology
  • Adiponectin / genetics
  • Adiponectin / metabolism
  • Cell Differentiation / genetics
  • Cell Proliferation / genetics
  • Cells, Cultured
  • Chemokines / genetics
  • Chemokines / metabolism
  • Cytokines / genetics
  • Cytokines / metabolism
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Leptin / genetics
  • Leptin / metabolism
  • Macrophages / metabolism
  • Macrophages / pathology
  • Nicotinamide Phosphoribosyltransferase / genetics
  • Nicotinamide Phosphoribosyltransferase / metabolism
  • Obesity / genetics*
  • Obesity / metabolism
  • Obesity / pathology
  • Retinol-Binding Proteins, Plasma / genetics
  • Retinol-Binding Proteins, Plasma / metabolism
  • Stem Cells / metabolism*
  • Stem Cells / pathology
  • Subcutaneous Fat / metabolism*
  • Subcutaneous Fat, Abdominal / metabolism*
  • Subcutaneous Fat, Abdominal / pathology
  • beta-Defensins / genetics
  • beta-Defensins / metabolism

Substances

  • ADIPOQ protein, human
  • Adiponectin
  • Chemokines
  • Cytokines
  • DEFB1 protein, human
  • Intercellular Signaling Peptides and Proteins
  • Leptin
  • RARRES2 protein, human
  • RBP4 protein, human
  • Retinol-Binding Proteins, Plasma
  • beta-Defensins
  • Nicotinamide Phosphoribosyltransferase
  • nicotinamide phosphoribosyltransferase, human