Exosomes are now considered an important subcategory of extracellular vesicles (ECVs) that contain a core of micro-RNA (miRNA), messenger-RNA (mRNA), transcription factors, membrane-trafficking proteins, antigen-presenting proteins, and other peptides protected within a bilayer lipid membrane. To date, exosomes have displayed a plethora of prospective clinical applications, including stem cell maintenance and plasticity, biomarkers, adjuncts in chemotherapy and drug delivery, and wound healing supplements that promote angiogenesis.
Figure 1 Diagrammatic representation of the skin structure and the molecular composition of exosomes1.
CD Bioparticles can provide you with high purity exosomes with unique advantages, especially high stability, intrinsic bioactivity and easy absorption.
Exposure to the external environment may lead to instability and dysfunction of the skin, resulting in refractory wound, skin aging, pigmented dermatosis, hair loss, some immune-mediated dermatoses, and connective tissue diseases. Nowadays, many skin treatments have not achieved a commendable balance between medical recovery and cosmetic needs. Exosomes are cell-derived nanoscale vesicles carrying various biomolecules, including proteins, nucleic acids, and lipids, with the capability to communicate with adjacent or distant cells. Recent studies have demonstrated that endogenic multiple kinds of exosomes are crucial orchestrators in shaping physiological and pathological development of the skin. Besides, exogenous exosomes, such as stem cell exosomes, can serve as novel treatment options to repair, regenerate, and rejuvenate skin tissue1.
EVs and miRNA-based cross-talk between keratinocytes and melanocytes are implicated in inhibiting pigmentation. UV radiation can also regulate the light-dependent function of keratinocyte-derived EVs2.
EVs released by various cell types, including macrophages and fibroblasts, play a role in scar formation. EVs derived from adipose-derived stem cells (ADSC-exos) and mesenchymal stem cells (MSC-Ex) accelerate scar healing. EVs derived from hucMSCs promote skin cell proliferation and migration through Wnt43.
Autologous HDF extracellular vesicle therapy improves facial contour and slows down skin aging by regulating TIMP-1, miRNAs, TNF-α, and TGF-β expression. Embryonic stem cell-derived mmu-miR-291a-3p inhibits cellular senescence in human skin fibroblasts through the TGF-β receptor 2 pathway4.
DPC-derived extracellular vesicles (DPC-Exos) accelerate hair follicle growth and development by regulating the growth and cycling of hair follicle stem cells (HFSCs) and dermal papilla cells (DPCs)5.
For example, in the case of dermal fillers or botulinum toxin injections, exosomes may play a role in improving the effectiveness or duration of the effects.
We offer a range of testing services to support the evaluation of exosome activity, both in vitro and in vivo. Our services include:
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