J. Mater. Sci. Technol. ›› 2021, Vol. 78: 110-120.DOI: 10.1016/j.jmst.2020.10.054
• Review Article • Previous Articles Next Articles
Ya Zhaoa, Yonghua Suna, Weiwei Lanb, Zhong Wanga, Yi Zhanga, Di Huangb,*(
), Xiaohong Yaoa, Ruiqiang Hanga,*()
Received:2020-08-27
Revised:2020-10-27
Accepted:2020-10-30
Published:2021-07-10
Online:2020-11-21
Contact:
Di Huang,Ruiqiang Hang
About author:hangruiqiang@tyut.edu.cn(R. Hang).Ya Zhao, Yonghua Sun, Weiwei Lan, Zhong Wang, Yi Zhang, Di Huang, Xiaohong Yao, Ruiqiang Hang. Self-assembled nanosheets on NiTi alloy facilitate endothelial cell function and manipulate macrophage immune response[J]. J. Mater. Sci. Technol., 2021, 78: 110-120.
Fig. 1. (a) SEM images. (b) XPS survey spectra. (c) High-resolution XPS spectra of Ti 2p. (d) High-resolution XPS spectra of Ni 2p. (e) High-resolution XPS spectra of K 2p.
| Sample | Atomic concentrations (at.%) | ||||||
|---|---|---|---|---|---|---|---|
| C | N | K | Ni | O | Ti | Ni/Ti | |
| NiTi-MP | 42.16 | 2.02 | - | 2.73 | 46.40 | 6.69 | 0.41 |
| AC-2.5 M | 54.61 | 2.20 | 2.21 | 7.03 | 32.50 | 1.45 | 4.85 |
| AC-5 M | 52.98 | 2.57 | 3.44 | 6.51 | 32.98 | 1.52 | 4.28 |
| AC-15 M | 37.92 | - | 3.11 | 9.64 | 45.04 | 4.29 | 2.25 |
Table 1 Elemental concentrations (at.%) on the surface of all the samples.
| Sample | Atomic concentrations (at.%) | ||||||
|---|---|---|---|---|---|---|---|
| C | N | K | Ni | O | Ti | Ni/Ti | |
| NiTi-MP | 42.16 | 2.02 | - | 2.73 | 46.40 | 6.69 | 0.41 |
| AC-2.5 M | 54.61 | 2.20 | 2.21 | 7.03 | 32.50 | 1.45 | 4.85 |
| AC-5 M | 52.98 | 2.57 | 3.44 | 6.51 | 32.98 | 1.52 | 4.28 |
| AC-15 M | 37.92 | - | 3.11 | 9.64 | 45.04 | 4.29 | 2.25 |
Fig. 2. TEM and HR-TEM images and SAED patterns of the samples.
Fig. 3. (a) Water contact angles of the samples. (b) Histogram of Ni2+ release concentrations from all the samples for 24 h. *p < 0.05 when compared with NiTi-MP, **p < 0.01 when compared with NiTi-MP, $$p < 0.01 when compared with AC-2.5 M, @@p < 0.01 when compared with AC-5 M.
Fig. 4. (a) Fluorescence images of nuclei after incubation for 4 h. (b) Quantitative results of cell adhesion. (c) Fluorescence images of cytoskeleton (green) and nuclei (blue) of ECs cultured on the sample surfaces for 24 h. (d) FE-SEM images of ECs after culturing on the sample surfaces for 24 h. (e) Fluorescence images of live/dead staining of ECs cultured on the sample surfaces. (f) CCK-8 results of ECs after culturing on the sample surfaces for 1, 3, and 5 days. *p < 0.05 when compared with NiTi-MP, **p < 0.01 when compared with NiTi-MP, $p < 0.05 when compared with AC-2.5 M, $$p < 0.01 when compared with AC-2.5 M, @p < 0.01 when compared with AC-5 M, @@p < 0.01 when compared with AC-5 M.
Fig. 5. (a) Representative fluorescence images of NO in ECs stained by DAF-FM DA after culturing on the sample surfaces for 1 day. (b) Mean fluorescence intensity of NO in ECs. (c) VEGF concentrations secreted by ECs after culturing on the sample surfaces for 1 day. (d) Fluorescence images showing the migration of ECs cultured on different sample surfaces. (e) Quantitative results of migration distance of ECs. *p < 0.05 when compared with NiTi-MP, **p < 0.01 when compared with NiTi-MP, $p < 0.05 when compared with AC-2.5 M, $$p < 0.01 when compared with AC-2.5 M, @@p < 0.01 when compared with AC-5 M.
Fig. 6. (a) Optical images of ECs after incubation on the matrix gel for 4, 8, 12, and 18 h. (b)-(e) histograms of the numbers of nodes, circles, and tubes formed by ECs after incubated in the gel for 4, 8, 12, and 18 h on the gel. *p < 0.05 when compared with NiTi-MP; **p < 0.01 when compared with NiTi-MP; $p < 0.05 when compared with AC-2.5 M; $$p < 0.01 when compared with AC-2.5 M; @p < 0.05 when compared with AC-5 M; @@p < 0.01 when compared with AC-5 M.
Fig. 7. (a) SEM images showing the morphology of macrophages after culturing on the sample surfaces for 1 day. (b) The expression of inflammatory genes (IL-1β, TNF-α, IL-18, and IL-6), M1 markers (CD11, CCR-7, iNOS, and CD86), M2 markers (IL-10, CD163, CD206, and ARG1), and growth factors (TGF-β, BMP2, and VEGF) in macrophages after culturing on the sample surfaces for 1 day.
Fig. 8. The influence of the macrophage-conditioned medium on ECs. (a) Fluorescence images of live/dead staining of ECs after culturing for 1 and 3 days. (b) CCK-8 results of ECs after culturing for 1 and 3 days. (c) Fluorescence images of NO in ECs stained by DAF-FM DA after culturing for 1 day. (d) Mean fluorescence intensity of NO in ECs. (e) Quantitative results of VEGF secretion of ECs after culturing for 1 day. (f) Optical images of EC migration. (g) Migration distance of ECs. (h) Angiogenic-related gene expression of ECs after culturing for 1 day. *p < 0.05 when compared with NiTi-MP, **p < 0.01 when compared with NiTi-MP, $p < 0.05 when compared with AC-2.5 M, $$p < 0.01 when compared with AC-2.5 M, @p < 0.05 when compared with AC-5 M, @@p < 0.01 when compared with AC-5 M.
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