Frozen Fat Tissue Yields Healthy Stem Cells for Future Use
Jasmin Bagge, Per Hölmich, Freja Aabæk Hammer, Jan O. Nehlin, Kilian Vomstein, Lars Blønd, Lisbet Rosenkrantz Hölmich, Kristoffer Weisskirchner Barfod · Journal of Experimental Orthopaedics · 2023
Researchers test if regenerative cells survive deep freezing
For patients with knee osteoarthritis considering Lipogems® treatment, an important question is whether fat tissue can be safely stored for future use. This Danish study explored whether stem cells remain healthy and functional after freezing micro-fragmented adipose tissue (specially processed fat) for extended periods.
The research team collected abdominal fat tissue from seven patients with knee osteoarthritis. The fat was processed using the Lipogems® system, then frozen at minus 80 degrees Celsius. Samples remained frozen between 46 and 150 days. After thawing, scientists tested two methods for extracting stem cells from the tissue.
All seven patients' samples produced viable stem cells
The most encouraging finding was that every single patient's frozen tissue sample yielded healthy, living stem cells. This 100% success rate suggests that cryopreservation (medical freezing) does not destroy the regenerative potential of micro-fragmented fat tissue.
The extracted cells showed low levels of senescence markers. Senescence means cellular aging or breakdown. Low levels indicate the cells remained "young" and functional despite the freezing process.
Cells multiplied normally and maintained healing abilities
Scientists tracked how well the recovered stem cells could grow and divide. Population doubling time—how long cells take to multiply—remained normal through multiple growth cycles. This matters because treatment often requires expanding cell numbers in the laboratory.
The cells also passed critical function tests:
They successfully transformed into bone-forming cells
They successfully transformed into fat cells
These abilities confirm the cells retained their regenerative "stemness"
Multiple healing cell types survived the freezing process
The research identified four distinct stem cell populations in the thawed tissue:
Adventitial stem cells (cells surrounding blood vessels)
Pericytes (helper cells supporting blood vessel healing)
Transitional pericytes (cells shifting between types)
CD271+ stem cells (cells with strong bone-building potential)
Finding pericytes is particularly relevant. These cells play key roles in tissue repair and are considered clinically important for treating joint conditions.
One extraction method preserved more pericytes
The study compared two techniques for removing stem cells from thawed tissue. Tissue explant culture (letting cells migrate out naturally) preserved significantly more pericytes than enzymatic digestion (using chemicals to break down tissue). At passage four, tissue explant culture yielded 25% pericytes compared to only 3% with enzymatic digestion.
This eightfold difference could influence future treatment preparation. Higher pericyte numbers may translate to better healing outcomes, though this requires further clinical study.
What this means for your treatment decision
This laboratory study offers promising news for knee osteoarthritis patients. Freezing micro-fragmented fat tissue does not appear to destroy its regenerative cells. All key stem cell types that support joint healing survived the process.
For practical purposes, this research suggests future possibilities:
Fat tissue harvested during one procedure could potentially supply multiple treatments
Younger, healthier tissue might be stored for use later in life when osteoarthritis worsens
Repeated treatments—which some studies link to better long-term results—might not require additional liposuction procedures
However, this was a laboratory study with seven patients. It did not test whether frozen-then-thawed cells work as effectively as fresh cells when injected into arthritic knees. The researchers also note that no randomized controlled trials have yet proven the clinical effectiveness of micro-fragmented fat treatment for knee osteoarthritis.
Patients considering Lipogems® should discuss current evidence with their physician. This study adds valuable knowledge about tissue preservation but does not change existing treatment recommendations.
Source: Bagge et al., Journal of Experimental Orthopaedics, 2023.
Original Publication
Successful isolation of viable stem cells from cryopreserved microfragmented human adipose tissue from patients with knee osteoarthritis - a comparative study of isolation by tissue explant culture and enzymatic digestion
Jasmin Bagge, Per Hölmich, Freja Aabæk Hammer, Jan O. Nehlin, Kilian Vomstein, Lars Blønd, Lisbet Rosenkrantz Hölmich, Kristoffer Weisskirchner Barfod · Journal of Experimental Orthopaedics · 2023
This study investigated whether viable stem cells could be isolated and expanded from cryopreserved microfragmented adipose tissue (AT) harvested from knee osteoarthritis patients. Microfragmented abdominal AT from 7 patients was cryopreserved at -80°C for 46-150 days (mean 115.9 days). Stem cells were isolated using two methods: tissue explant culture (TEC) and enzymatic digestion (ED). Viability, population doublings, doubling time, cell type, senescence-associated β-galactosidase activity, and osteogenic and adipogenic differentiation capacity were assessed through trypan blue staining, flow cytometry, and histological staining. Viable stem cells were successfully recovered and expanded from all patients using both isolation methods, with no significant difference in viable population doublings or doubling time from passage 1 to 3. Low senescence levels were detected for both methods. Stemness was confirmed by stem cell surface markers and differentiation performance. Multiple stem cell populations were identified, including adventitial stem cells, pericytes, transitional pericytes, and CD271⁺ stem cells. TEC yielded significantly more pericytes (25%) compared to ED (3%) at passage 4. The study demonstrates that viable stem cells can be successfully isolated and expanded from cryopreserved microfragmented AT using both methods, with TEC providing more clinically relevant pericytes than ED.