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Table 4 Different sources of sEVs and their application in cartilage regeneration

From: The role of the immune microenvironment in bone, cartilage, and soft tissue regeneration: from mechanism to therapeutic opportunity

Source

Cell experiment

Animal experiment

Utilization

Roles of sEVs in tissue regeneration

Potential mechanisms

Embryonic stem cell-derived MSCs

Chondrocytes;

5 µg/ml

Rat; dose:

2 mg/ml

Osteoarthritis treatment [232]

Promote temporomandibular joint repair and regeneration [232]

Ameliorate inflammation and suppress apoptosis and matrix degradation to achieve overall joint homeostasis [232]

MSCs

Primary chondrocytes; 10 µg/ml

–

Osteoarthritis treatment [233]

Promote chondrocytes proliferation [233]

Activation of miR-206/GIT1 axis [233]

Primary MSCs

Primary chondrocytes; 50 µg/ml

–

Osteoarthritis treatment [234]

Promote chondrogenesis and enhance chondrocytes proliferation [234]

Inhibit HDAC2/8 expression and promote cartilage matrix expression [234]

Embryonic stem cell-derived MSCs

-

Rat model; dose:

1 mg/ml

Cartilage regeneration [235]

Promote cartilage and subchondral bone repair [235]

–

Embryonic stem cell-derived MSCs

Primary chondrocytes; 0.1, 0.5 and 1.0 µg/ml

Rat model; dose:

1 mg/ml

Cartilage regeneration [236]

Promote chondrocytes proliferation and ameliorate inflammation [236]

Coordinated mobilization of multiple cell types and activation of several cellular processes [236]

MSCs

HUVECs;

100 µg/ml

–

Regeneration [237]

Promote angiogenesis [237]

Mediate stem cell-endothelial cell crosstalk [237]

Serum

MSCs, chondrocytes

–

Cartilage regeneration [238]

Promote MSCs towards chondrogenic differentiation [238]

Deliver sEVs-derived miR-140 to MSCs [238]

  1. – No data. SEVs small extracellular vesicles, MSCs mesenchymal stem cells, HDAC2 recombinant histone deacetylase 2, HUVECs human umbilical vein endothelial cells