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Analysis of Fat Graft Survival and Platelet-Rich Plasma Effects: The Transcriptomic Differences.
Yegin, Ecem E; Yegin, Mehmet E; Kosova, Buket; Gür, Ersin; Nuriyev, Urfat.
Afiliação
  • Yegin EE; Bioinformatics, Ege University, Izmir, TUR.
  • Yegin ME; Plastic, Reconstructive and Aesthetic Surgery, Ege University Faculty of Medicine, Izmir, TUR.
  • Kosova B; Medical Biology, Ege University, Izmir, TUR.
  • Gür E; Plastic, Reconstructive and Aesthetic Surgery, Ege University, Izmir, TUR.
  • Nuriyev U; Computer Sciences, Ege University Faculty of Science, Izmir, TUR.
Cureus ; 15(1): e34380, 2023 Jan.
Article em En | MEDLINE | ID: mdl-36874761
ABSTRACT

INTRODUCTION:

Fat graft survival has been studied numerously but has not gone beyond hypothetical solutions. The molecular changes in survival of standard fat grafts and enhanced survival by platelet-rich plasma (PRP) are compared in this study to reveal the etiology that causes the loss of fat grafts after transplantation. MATERIALS AND

METHODS:

A New Zealand rabbit's inguinal fat pads were excised and divided into three groups Sham, Control (C), and PRP. Each weighing 1 g, C and PRP fat were placed into the bilateral parascapular area of the rabbit. After 30 days, the remaining fat grafts were harvested and weighed (C = 0.7 g, PRP = 0.9 g). All three specimens were put into transcriptome analysis. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes Analysis were done to compare the genetic pathways between the specimens.

RESULTS:

Transcriptome analysis showed similar differential expressions in Sham vs. PRP and Sham vs. C comparisons, indicating the dominance of the cellular immune response in both C and PRP specimens. C and PRP comparison resulted in inhibited migration and inflammation pathways in PRP.

CONCLUSION:

Fat graft survival is more related to immune responses than any other physiological process. PRP enhances survival by attenuating cellular immune reactions.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cureus Ano de publicação: 2023 Tipo de documento: Article