Peipei He

Fe-based coatings have been prepared by utilizing laser cladding with the scanning speed ranging from 1.57 to 20.4 m/min. The microstructure and corrosion properties have been further investigated to evaluate the effects of scanning speed. The results show that, both coating's thickness and dilution rate gradually decrease with the increase of scanning speed. However, the deposition efficiency on the surface can be greatly improved by around 4 times. Under high scanning speed, the Fe-based coatings show the similar microstructure feature, comprising with dendrites and inter-dendritic structures. But the coating's microstructure can be significantly refined with the secondary dendritic arm spacing less than 1 μm. Furthermore, the gap of Cr concentration between the two structures can be effectively reduced, which shrinks the difference in corrosion resistance. On the other hand, the Fe-based coating's hardness gradually decreases resulting from the retained austenite and ferrite under high scanning speed. Compared to Q235 steel, the cladded Fe-based coatings show superior corrosion resistance with much higher corrosion potential and lower corrosion current density. Pitting dominates the corrosion forms of high-speed laser Fe-based coatings, which initially takes place on the boundaries of different structures. With the increase of scanning speed, the coating's corrosion resistance increases firstly and then decreases, and the coating cladded with the speed of 15.7 m/min shows the best corrosion resistance. Higher average Cr content and more uniform Cr distribution account for the better corrosion resistance. However, excessive microstructure refinement plays a negative role in the coating's corrosion resistance owing to more grain boundaries.

Background: In the bone marrow microenvironment of postmenopausal osteoporosis (PMOP), bone marrow mesenchymal stem cell (BMSC)-derived exosomal miRNAs play an important role in bone formation and bone resorption, although the pathogenesis has yet to be clarified. Methods: BMSC-derived exosomes from ovariectomized rats (OVX-Exo) and sham-operated rats (Sham-Exo) were co-cultured with bone marrow-derived macrophages to study their effects on osteoclast differentiation. Next-generation sequencing was utilized to identify the differentially expressed miRNAs (DE-miRNAs) between OVX-Exo and Sham-Exo, while target genes were analyzed using bioinformatics. The regulatory effects of miR-27a-3p and miR-196b-5p on osteogenic differentiation of BMSCs and osteoclast differentiation were verified by gain-of-function and loss-of-function analyses. Results: Osteoclast differentiation was significantly enhanced in the OVX-Exo treatment group compared to the Sham-Exo group. Twenty DE-miRNAs were identified between OVX-Exo and Sham-Exo, among which miR-27a-3p and miR-196b-5p promoted the expressions of osteogenic differentiation markers in BMSCs. In contrast, knockdown of miR-27a-3p and miR-196b-5p increased the expressions of osteoclastic markers in osteoclast. These 20 DE-miRNAs were found to target 11435 mRNAs. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses revealed that these target genes were involved in several biological processes and osteoporosis-related signaling pathways. Conclusion: BMSC-derived exosomal miR-27a-3p and miR-196b-5p may play a positive regulatory role in bone remodeling.