Published online Dec 15, 2024. doi: 10.4239/wjd.v15.i12.2399
Revised: September 27, 2024
Accepted: October 30, 2024
Published online: December 15, 2024
Processing time: 98 Days and 13 Hours
Diabetic osteoporosis (DOP) is a serious complication of diabetes mellitus. It is urgent to explore efficient clinical treatment strategies for DOP. It has been found that mesenchymal stem cell-derived extracellular vesicles (MSC-EVs), as an emerging cell-free therapy, show great potential in DOP treatment. MSC-EVs can effectively promote bone formation, inhibit bone resorption, and modulate the inflammatory microenvironment by delivering cargoes of microRNAs, long non-coding RNAs, and proteins to target cells, thereby ameliorating bone loss in DOP. However, there are limited reports on the treatment of DOP with MSC-EVs. To evoke more attention to this potential strategy, this article summarised the extant literature on MSC-EVs for DOP to provide new directions for further research and to promote the application of MSC-EVs in the clinical management of DOP.
Core Tip: A sustained high-glucose microenvironment may impair bone homeostasis leading to the initiation and progression of diabetic osteoporosis (DOP) in patients with diabetes mellitus (DM). Correcting the uncoupled bone remodelling and inflammatory microenvironment is the key to treating DOP. Mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) have received widespread attention due to their ability to promote bone regeneration and inhibit bone loss in the treatment of osteoporosis by targeting the delivery of modifiable cargoes. This suggests that MSC-EVs also have great potential for the treatment of DOP, although the condition of DOP patients is more complex due to the fact that DOP patients are usually also accompanied by multiple cardiovascular and cerebrovascular complications and long-term use of multiple medications. Rapid advances in genetic engineering and bioengineering have also enabled modifiable MSC-EVs to show significant advantages in personalised and tailored treatment cases. More studies are needed to further demonstrate and develop the clinical therapeutic potential of MSC-EVs in DOP.