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Updated: Dec 31, 2025

Isolation, Expansion, and Differentiation of Mesenchymal Stem Cells from the Infrapatellar Fat Pad of the Goat Stifle Joint
Published on: August 2, 2022
Infrapatellar Fat Pad Stem Cells Responsiveness to Microenvironment in Osteoarthritis: From Morphology to Function
Elena Stocco1,2,3, Silvia Barbon1,2,3, Monica Piccione4
1Department of Neurosciences, Institute of Human Anatomy, University of Padova, Padua, Italy.
Stem cells from osteoarthritic infrapatellar fat pads (OA-IFP) show potential for cartilage regeneration but may be reprogrammed by inflammation. These cells exhibit some protective responses but have limited ability to counteract OA-related inflammation.
Area of Science:
- Biomedical Engineering
- Regenerative Medicine
- Cell Biology
Background:
- Infrapatellar fat pad (IFP) stem cells are explored for cartilage regeneration in osteoarthritis (OA).
- OA's inflammatory environment may alter stem cell properties and function.
Purpose of the Study:
- To characterize the structural and functional properties of stem cells from osteoarthritic IFP (OA-IFP).
- To investigate the impact of the OA pathological environment on these stem cells.
Main Methods:
- Isolation and characterization of OA-IFP stem cells from nine OA patients undergoing knee arthroplasty.
- Analysis included morphology, stemness markers, metabolic profile, and multi-differentiation potential via electron microscopy, flow cytometry, gene expression, and cytochemistry.
Main Results:
- OA-IFP stem cells displayed spindle morphology, self-renewal, and responsiveness to stimuli.
- High stemness markers (STAT3, NOTCH1, c-Myc, OCT-4, KLF4, NANOG) and specific immunophenotype (CD73+, CD39+, CD90+, CD105+, CD44-/+, CD45-).
- Inflammation-induced reprogramming suggested by HLA-DR, CD34, Fas, FasL expression; potential mechanical stress response (COL1A1); limited ability to counteract inflammation (low CD38/NADase).
Conclusions:
- OA-IFP stem cells are primed by the pathological OA environment.
- These cells may offer incomplete protection against OA inflammation and mechanical stress.
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