2 research outputs found
Accelerated Bone Regeneration by Two-Photon Photoactivated Carbon Nitride Nanosheets
Human bone marrow-derived mesenchymal
stem cells (hBMSCs) present
promising opportunities for therapeutic medicine. Carbon derivatives
showed only marginal enhancement in stem cell differentiation toward
bone formation. Here we report that red-light absorbing carbon nitride
(C<sub>3</sub>N<sub>4</sub>) sheets lead to remarkable proliferation
and osteogenic differentiation by runt-related transcription factor
2 (Runx2) activation, a key transcription factor associated with osteoblast
differentiation. Accordingly, highly effective hBMSCs-driven mice
bone regeneration under red light is achieved (91% recovery after
4 weeks compared to 36% recovery in the standard control group in
phosphate-buffered saline without red light). This fast bone regeneration
is attributed to the deep penetration strength of red light into cellular
membranes <i>via</i> tissue and the resulting efficient
cell stimulation by enhanced photocurrent upon two-photon excitation
of C<sub>3</sub>N<sub>4</sub> sheets near cells. Given that the photoinduced
charge transfer can increase cytosolic Ca<sup>2+</sup> accumulation,
this increase would promote nucleotide synthesis and cellular proliferation/differentiation.
The cell stimulation enhances hBMSC differentiation toward bone formation,
demonstrating the therapeutic potential of near-infrared two-photon
absorption of C<sub>3</sub>N<sub>4</sub> sheets in bone regeneration
and fracture healing
Additional file 1: of The transcriptional profile of coronary arteritis in Kawasaki disease
Supplemental Methods. Table S1. RNA sequencing metrics. Table S2. All differentially expressed genes (8 KD cases vs 7 controls). Table S3. Dysregulated molecular pathways (8 KD cases vs 7 controls). Table S4. Differential expression of genes involved in antigen presentation and dendritic cell function in KD compared to control coronary arteries by real-time reverse transcriptase PCR assays. Table S5. Extracellular genes dysregulated in 8 KD coronary arteries compared with 7 childhood control coronary arteries. Figure S1. Principal components analysis of all genes in 8 KD (4 treated and 4 untreated) and 7 childhood control coronary artery tissues demonstrates that gene expression of untreated (red dots) and treated (black dots) KD patients are not distinguishable. (PDF 382 kb