# Histological and Immunohistochemical Characteristics of Mechanically Processed Adipose Tissue: A Systematic Review and Meta-Analysis

**Authors:** Tom Schimanski, Rafael Loucas, Marios Loucas, Vanessa Brébant, Alexandra Anker, Silvan Klein, Sophia Theresa Diesch, Andrea Pagani, Lukas Prantl

PMC · DOI: 10.3390/cells14211664 · Cells · 2025-10-23

## TL;DR

This study reviews how mechanical processing affects fat tissue structure and cell markers, finding benefits like better cell preservation and fewer harmful features.

## Contribution

The study systematically reviews and summarizes the histological and immunohistochemical effects of mechanical processing on adipose tissue.

## Key findings

- Mechanically processed adipose tissue shows increased stromal vascular fraction cell density in most studies.
- Processing improves extracellular matrix preservation and reduces mature adipocytes and inflammatory features.
- Elevated vascular marker and perilipin expression is observed in processed fat.

## Abstract

Background: Mechanical processing techniques are commonly employed to prepare adipose tissue for clinical applications in reconstructive and aesthetic procedures. However, their histological and immunohistochemical impact on adipose tissue remains incompletely characterized. Purpose: This systematic review aims to investigate the impact of mechanical processing on the histological and immunohistochemical properties of adipose tissue. Methods: A systematic search was conducted using PubMed, Ovid, and Cochrane Library databases, with publications up to December 2024, employing Boolean operators (“mechanically processed” OR “lipoaspirate” OR “fat graft” OR “gauze rolling” OR “decantation” OR “coleman fat” OR “celt” OR “nanofat” OR “lipofilling” OR “human fat”) AND (“histol*”). Included were English-language studies or studies with a recognized English translation which had been subject to peer review and reported quantitative or qualitative markers of mechanically processed human adipose tissue with histology or immunohistochemistry. Risk of Bias was assessed with the OHAT score. Results: A total of 15 studies (n = 15) were included. In 13 of 15 studies (87%), mechanically processed adipose tissue demonstrated an increased stromal vascular fraction (SVF) cell density compared to unprocessed fat. Twelve studies (80%) reported improved preservation of the extracellular matrix (ECM), while 11 studies (73%) observed a reduction in mature adipocytes. Immunohistochemical analyses in 10 studies (67%) revealed elevated expression of vascular markers (CD31, CD34) and perilipin. Adverse histological features such as oil cysts, fibrosis, and inflammatory infiltrates were reduced in 9 studies (60%). Considerable heterogeneity in processing techniques and staining protocols precluded meta-analysis. Conclusions: Mechanical processing of adipose tissue is associated with favorable histological and immunohistochemical profiles, including increased SVF cell density, improved ECM preservation, and reduced inflammatory and fibrotic features. These findings support the potential of mechanical processing to enhance graft quality; however, standardization of techniques and evaluation protocols is needed to strengthen clinical translation.

## Linked entities

- **Proteins:** PECAM1 (platelet and endothelial cell adhesion molecule 1), CD34 (CD34 molecule), plin1 (perilipin 1)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CD34 (CD34 molecule) [NCBI Gene 947], PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, PLIN1 (perilipin 1) [NCBI Gene 5346] {aka FPLD4, PERI, PLIN}
- **Diseases:** oil cysts (MESH:D003560), inflammatory (MESH:D007249), fibrosis (MESH:D005355)
- **Chemicals:** lipoaspirate (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12608007/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12608007/full.md

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Source: https://tomesphere.com/paper/PMC12608007