Perilipin2 is an Earlier Marker Than Perilipin1 for Identifying Adipocyte Regeneration in Fat Grafts

Aesthet Surg J. 2021 May 18;41(6):NP646-NP652. doi: 10.1093/asj/sjaa360.

Abstract

Background: Both perilipin1 (Plin1) and perilipin2 (Plin2) play a crucial role in regulating lipid droplet (LD) formation in fat cells. Plin2 is expressed early in the adipocyte differentiation process but is replaced by Plin1 after cell maturation. In free fat grafts, only a small number of adipocytes remain alive or are replaced by newly regenerated fat cells. It is known that Plin1-positive adipocytes participate in regeneration, but the characteristics of Plin2 expression during this process are still poorly understood.

Objectives: The aim of this study was to investigate whether Plin2 is a more precise early marker for detecting adipocyte regeneration in fat grafts than Plin1.

Methods: Autologous fat tissue (120 mg) harvested from inguinal fat pads was injected under the scalps of C57 mice. Samples were explanted at days 3, 7, 15, and 30 after transplantation. Changes in sample size and weight were evaluated. Hematoxylin-eosin staining, real-time polymerase chain reaction, and immunostaining of Plin1 and Plin2 expression were performed.

Results: Plin1, but not Plin2, expression was detected in the freshly harvested fat, but the latter was activated after grafting. Newly regenerated Plin2-positive adipocytes increased from day 3 to day 7 and then declined, whereas the number of Plin1-positive fat cells decreased first and began to increase after day 15. The expression levels of Plin1 and Plin2 mRNA demonstrated similar changes over time. At day 30, adipocytes lost Plin2 expression and were positive for Plin1 again.

Conclusions: Our experiments showed convincing evidence that Plin2 expression could be used to detect early adipocyte regeneration in grafted fat tissue.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes*
  • Adipose Tissue / transplantation*
  • Animals
  • Cell Differentiation
  • Mice
  • Perilipin-1 / genetics
  • Perilipin-2 / genetics*
  • RNA, Messenger
  • Regeneration*

Substances

  • Perilipin-1
  • Perilipin-2
  • Plin1 protein, mouse
  • Plin2 protein, mouse
  • RNA, Messenger