Adipose tissue-derived microvascular fragments promote lymphangiogenesis in a murine lymphedema model.
Florian Samuel FruehLaura GassertClaudia ScheuerAndreas MüllerPeter FriesAnne S BoeweEmmanuel AmpofoClaudia E RübeMichael D MengerMatthias W LaschkePublished in: Journal of tissue engineering (2022)
Chronic lymphedema after cancer treatment is common and there is still no cure for this disease. We herein investigated the lymphangiogenic capacity of adipose tissue-derived microvascular fragments (MVF), which contain stem cells and lymphatic vessel fragments. Secondary lymphedema was induced in the hindlimbs of C57BL/6J mice. Green fluorescence protein (GFP) + MVF were isolated from transgenic C57BL/6Tg (CAG-EGFP)1Osb/J mice, suspended in collagen hydrogel, and injected in the lymphadenectomy defect of wild-type animals. This crossover model allowed the detection of MVF-derived blood and lymphatic vessels after transplantation. The MVF group was compared with animals receiving collagen hydrogel only or a sham intervention. Lymphangiogenic effects were analyzed using volumetry, magnetic resonance (MR) lymphography, histology, and immunohistochemistry. MVF injection resulted in reduced hindlimb volumes when compared to non-treated controls. MR lymphography revealed lymphatic regeneration with reduced dermal backflow after MVF treatment. Finally, MVF transplantation promoted popliteal angiogenesis and lymphangiogenesis associated with a significantly increased microvessel and lymphatic vessel density. These findings indicate that MVF transplantation represents a promising approach to induce therapeutic lymphangiogenesis.
Keyphrases
- adipose tissue
- lymph node
- stem cells
- wound healing
- magnetic resonance
- wild type
- cell therapy
- randomized controlled trial
- insulin resistance
- endothelial cells
- high fat diet induced
- clinical trial
- high fat diet
- squamous cell carcinoma
- high glucose
- metabolic syndrome
- single molecule
- hyaluronic acid
- lymph node metastasis
- single cell
- mass spectrometry
- open label
- study protocol
- protein protein
- newly diagnosed
- skeletal muscle
- binding protein
- label free