Lab Study Compares Fat Tissue Preparations for Knee Cartilage Health
Lauren Kokai, Joseph Chen, Dong Wang, Sheri Wang, Francesco M. Egro, Benjamin Schilling, Hengyun Sun, Asim Ejaz, J. Peter Rubin, Jeffrey A. Gusenoff, Nam Vo, Kentaro Onishi, Gwendolyn Sowa · Stem Cells and Development · 2021
Researchers Test Three Methods for Processing Your Own Fat Tissue
Scientists at the University of Pittsburgh wanted to understand which fat tissue preparation works best for knee osteoarthritis. They tested three different methods in a laboratory setting. Each method processes fat tissue differently before it could potentially be injected into a damaged joint. Understanding these differences helps doctors choose the most effective treatment approach.
Cartilage Cells Respond Differently to Each Preparation
The research team used cartilage cells from two patients who had knee replacement surgery. They exposed these cells to three types of processed fat tissue:
SVF (Stromal Vascular Fraction): Fat tissue broken down using enzymes
Nanofat: Fat tissue squeezed through syringes to create tiny particles
Lipogems®: Fat tissue processed through a specialized bead-mill device
Each preparation contains regenerative cells, but the processing method affects how those cells interact with damaged cartilage.
Enzyme-Processed Fat Increased Inflammation in Cartilage
The study revealed a surprising finding about SVF, the enzyme-digested preparation. Cartilage cells exposed to SVF showed higher levels of inflammatory markers. These cells also produced more enzymes that break down cartilage tissue. This happened at both the 36-hour and 72-hour testing points. Higher inflammation and breakdown activity could potentially worsen joint damage rather than help healing.
Mechanically Processed Fat Promoted Cartilage Rebuilding
Both nanofat and Lipogems® showed more favorable results. Cartilage cells exposed to these preparations:
Showed minimal inflammatory response
Increased production of healthy cartilage building blocks
Demonstrated better balance between tissue breakdown and repair
This suggests that mechanical processing—using physical force rather than enzymes—preserves beneficial properties in the fat tissue.
Lipogems® Showed Most Consistent Regenerative Effects
While both mechanically processed preparations performed well, Lipogems® stood out for consistency. Nanofat produced temporary improvements in cartilage-building activity. However, Lipogems® maintained increased matrix synthesis at both study timepoints. Matrix synthesis means the cartilage cells were actively producing the structural proteins that make healthy cartilage strong and flexible. This sustained response suggests more reliable regenerative potential.
What This Laboratory Research Means for Patients
This study was conducted entirely in a laboratory, not in actual patients. Scientists grew cartilage cells in special gel beads to mimic natural conditions. They then observed how different fat preparations affected these cells over 36 to 72 hours. While laboratory studies cannot predict exactly what happens inside your body, they help researchers understand basic biological responses.
The findings suggest that how fat tissue gets processed matters significantly. Mechanical processing methods like Lipogems® may offer advantages over enzyme-based methods. The researchers noted that Lipogems® technology fragments fat tissue while preserving its natural structure. This keeps helpful cells like pericytes (cells that support blood vessel healing) and stem cells in their normal environment.
For patients considering regenerative treatments for knee osteoarthritis, this research provides encouraging laboratory evidence. It supports the use of mechanically processed fat tissue preparations. However, laboratory results need confirmation through clinical trials in actual patients. Talk with your doctor about whether Lipogems® treatment might be appropriate for your specific situation.
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Source: Kokai et al., Stem Cells and Development, 2021.
Original Publication
Comparison of Clinically Relevant Adipose Preparations on Articular Chondrocyte Phenotype in a Novel In Vitro Co-Culture Model
Lauren Kokai, Joseph Chen, Dong Wang, Sheri Wang, Francesco M. Egro, Benjamin Schilling, Hengyun Sun, Asim Ejaz, J. Peter Rubin, Jeffrey A. Gusenoff, Nam Vo, Kentaro Onishi, Gwendolyn Sowa · Stem Cells and Development · 2021
Adipose therapeutics, including isolated cell fractions and tissue emulsifications, have been explored for osteoarthritis (OA) treatment; however, the optimal preparation method and bioactive tissue component for healing has yet to be determined. This in vitro study compared the effects of adipose preparations on cultured knee chondrocytes. De-identified human articular chondrocytes were co-cultured with adipose preparations for 36 or 72 h. Human adipose tissues were obtained from abdominal panniculectomy procedures and processed using three different techniques: enzymatic digestion to release stromal vascular fraction (SVF), emulsification with luer-to-luer transfer (nanofat), and processing in a bead-mill (Lipogems, Lipogems International SpA, Milan, Italy). Gene expression in both chondrocytes and adipose preparations was measured to assess cellular inflammation, catabolism, and anabolism. Results demonstrated that chondrocytes cultured with SVF consistently showed increased inflammatory and catabolic gene expression compared with control chondrocytes at both 36- and 72-h timepoints. Alternatively, chondrocytes co-cultured with either nanofat or bead-mill processed adipose derivatives yielded minimal pro-inflammatory effects and instead increased anabolism and regeneration of cartilage extracellular matrix. Interestingly, nanofat preparations induced transient matrix anabolism while Lipogems adipose consistently demonstrated increased matrix synthesis at both study timepoints after co-culture. This evaluation of the regenerative potential of adipose-derived preparations as a clinical tool for knee OA treatment suggests that mechanically processed preparations may be more efficacious than an isolated SVF cell preparation.