BACKGROUND:Exosomes derived from mesenchymal stem cells are prospective cell-free alternatives for treating osteoarthritis.Their therapeutic activity and clinical transformation potential can be further improved by adjusting cell culture condition. OBJECTIVE:To review the effect of cell culture conditions on exosome activity and to analyze its clinical transformation potential. METHODS:Articles concerning osteoarthritis/cartilage repair and mesenchymal stem cell-derived exosomes were retrieved on CNKI and PubMed using"exosomes,mesenchymal stem cells,osteoarthritis or cartilage repair"as Chinese search terms and"exosomes or extracellular vesicles,mesenchymal stem cells,osteoarthritis or cartilage repair"as English search terms.The search time was from 2010 to 2023.Finally,100 articles were included for summary and analysis. RESULTS AND CONCLUSION:(1)During cell culture,providing a physical environment favorable for chondrocyte growth or adding chondroprotective small molecules,chondrogenic factors,or inflammatory factors,can further improve the regulatory activity of exosomes secreted by mesenchymal stem cells in maintaining chondrocyte phenotype,promoting cartilage regeneration,and immunosuppression.Therefore,other physical or chemical factors with similar characteristics may also improve the effects of exosomes secreted by mesenchymal stem cells for treating osteoarthritis.(2)Some treatments during cell culture,such as hypoxia induction,pulsed electromagnetic field stimulation,bioreactor,and chondroprotective molecule(e.g.,human parathyroid hormone 1-34)stimulation are safe and scalable,which allows for the production of clinical-grade exosomes secreted by mesenchymal stem cells for osteoarthritis treatment.(3)Mesenchymal stem cell exosomes are expected to achieve modified treatment of osteoarthritis,and the feasibility of clinical transformation can be further improved by adjusting the cell culture regimen to enhance the therapeutic activity.

Diabetic neuropathic pain (DNP) is the most common disabling complication of diabetes. Emerging evidence has linked the pathogenesis of DNP to the aberrant sprouting of sensory axons into the epidermal area; however, the underlying molecular events remain poorly understood. Here we found that an axon guidance molecule, Netrin-3 (Ntn-3), was expressed in the sensory neurons of mouse dorsal root ganglia (DRGs), and downregulation of Ntn-3 expression was highly correlated with the severity of DNP in a diabetic mouse model. Genetic ablation of Ntn-3 increased the intra-epidermal sprouting of sensory axons and worsened the DNP in diabetic mice. In contrast, the elevation of Ntn-3 levels in DRGs significantly inhibited the intra-epidermal axon sprouting and alleviated DNP in diabetic mice. In conclusion, our studies identified Ntn-3 as an important regulator of DNP pathogenesis by gating the aberrant sprouting of sensory axons, indicating that Ntn-3 is a potential druggable target for DNP treatment.
Mice ; Animals ; Diabetes Mellitus, Experimental/metabolism* ; Axons/physiology* ; Diabetic Neuropathies ; Sensory Receptor Cells/metabolism* ; Neuralgia/metabolism*

ObjectiveTo observe the clinicalefficacies of ginger-partitioned moxibustion in three different periods, i.e. the canicular days, the Spring Equinox, and the Autumnal Equinox, in treating allergic Rhinitis.MethodEighty-nine patients with allergic rhinitis were elected and divided into3 groups by using the random number table (canicular group, Spring Equinox group, and Autumnal Equinox group), to receive the same treatment with same point selection. The change of serum IgE and improvement of symptoms were observed after the intervention in the three groups.ResultThe three groups all showed significant decrease of serum IgE and improvement in the symptoms of allergic rhinitis (P<0.05), and the therapeutic efficacy of the canicular group was markedly higher than that of the Spring Equinox group (P<0.05) and the Autumnal Equinox group (P<0.05).ConclusionThe canicular days are the optimal timeperiodfor the treatment of allergicrhinitis.

Objective To observe the expression of 7 cytokeratins in skin epithelial tumors and to assess their diagnostic value. Methods The expression of 7 cytokeratins, including cytokeratin 7(K72.2), cytokeratin 8(C-51), cytokeratin 10(DE-K10), cytokeratin 14(LL002), cytokeratin 17(E3), cytokeratin 18(DC10)and cytokeratin 19(KS19.1), was assessed by immunohistochemical staining (S-P method) in 54 cases of different skin epithelial tumors and 20 normal skin specimens. Results Of 54 cases studied, 10 were squmous cell carcinoma (SCC), 10 basal cell carcinoma (BCC), 19 hair follicle tumor, 2 sebaceous carcinoma, and 13 sweat gland tumor. The expression patterns and distribution of the 7 cytokeratins were different in different skin epithelial tumors. Most of the tumor cells stained diffusely for cytokeratins in SCC, BCC and hair follicle tumor; different cytokeratins expressed in different parts of each of the subtypes of sweat gland tumors. Conclusions Analysis of a selected group of cytokeratins may be helpful in the diagnosis and differential diagnosis of SCC, basal cell carcinoma and skin adenexal tumor.