A field study on the composition, structure, and function of endophytic bacterial community of Robinia pseudoacacia at a composite heavy metals tailing.

Robinia pseudoacacia (R. pseudoacacia) is a well reported plant species for heavy metal phytoremediation, and it was capable to improve Cd uptake efficiency after inoculated with plant growth promoting endophytes. However, the knowledge on R. pseudoacacia associated endophytes in field condition and the relationship between these microbial communities and heavy metal uptake capacities are still scarce. In this study, the characteristics of heavy metal bioaccumulation and translocation in R. pseudoacacia, and the structure and function of its endophytic bacterial communities were revealed. The results showed that heavy metal pollution made microbes more sensitive to the environment as the diversity (Shannon) of endophyte community decreased but the abundance (Chao) increased. Redundancy analysis (RDA) also showed that heavy metals were the key factor affecting the composition of endophyte. In the co-occurrence network, 27 keystone taxa mainly from Actinobacteria, Proteobacteria and Firmicutes occupied the dominant niches, among which 16 OTUs mainly from lactobacillus, bacteroides, staphylococcus, methylorubrum and bifidobacterium were positively related to bioaccumulation and translocation of Cd, Cu, Pb and Zn. Besides, heavy metal stress enhanced the functional adaptability of endophytic bacteria community. Related predicted genes were enriched in immune response, physiological metabolism pathway and stress-resistant enzyme synthesis. This study showed that heavy metal stress enhanced the structural and functional adaptability of endophyte community and keystone taxa played significant role in improving the efficiency of phytoremediation.

A new broadband near-infrared emitting Mg2Al4Si5O18:Cr3+ phosphor for night-vision imaging.

Phosphor-converted light-emitting diodes (pc-LEDs) have important applications in security surveillance and food testing. However, developing new broadband near-infrared phosphors remains an important issue. Herein, the high-temperature solid-state reaction method was applied to synthesize a new type of Cr3+ doped Mg2Al4Si5O18 broadband NIR phosphor which matches a blue LED chip. It exhibits a broadband near-infrared (NIR) phosphor emission with a focus of 856 nm and a full width at half maximum >200 nm after excitation at 453 nm. The optimum concentration of Cr3+ was established to contain 2 mol%. At 398 K, the luminescence intensity is 45.2% of that at 298 K. The power output of NIR pc-LEDs fabricated by incorporating a 450 nm chip and the Mg2Al4Si5O18:0.02 Cr3+ phosphor is 19.69 mW at 300 mA current. Finally, the developed NIR pc-LED shows significant potential for use in night-vision imaging.

Cryogenic 3D printing of porous scaffolds for in situ delivery of 2D black phosphorus nanosheets, doxorubicin hydrochloride and osteogenic peptide for treating tumor resection-induced bone defects.

Tumor resection is widely used to prevent tumor growth. However, the defected tissue at the original tumor site also causes tissue or organ dysfunction which lowers the patient's life quality. Therefore, regenerating the tissue and preventing tumor recurrence are highly important. Herein, according to the concept of 'first kill and then regenerate', a versatile scaffold-based tissue engineering strategy based on cryogenic 3D printing of water-in-oil polyester emulsion inks, containing multiple functional agents, was developed, in order to realize the elimination of tumor cells with recurrence suppression and improved tissue regeneration sequentially. To illustrate our strategy, water/poly(lactic-co-glycolic acid)/dichloromethane emulsions containing ß-tricalcium phosphate (ß-TCP), 2D black phosphorus (BP) nanosheets, low-dose doxorubicin hydrochloride (DOX) and high-dose osteogenic peptide were cryogenically 3D printed into hierarchically porous and mechanically strong nanocomposite scaffolds, with multiple functions to treat bone tumor, resection-induced tissue defects. Prompt tumor ablation and long-term suppression of tumor recurrence could be achieved due to the synergistic effects of photothermotherapy and chemotherapy, and improved bone regeneration was obtained eventually due to the presence of bony environment and sustained peptide release. Notably, BP nanosheets in scaffolds significantly reduced the long-term toxicity phenomenon of released DOX during in vivo bone regeneration. Our study also provides insights for the design of multi-functional tissue engineering scaffolds for treating other tumor resection-induced tissue defects.

Liposomes Encapsulating Neoantigens and Black Phosphorus Quantum Dots for Enhancing Photothermal Immunotherapy.

Colorectal cancer frustrates with high relapse after the traditional treatment including surgery and chemotherapy. Neoantigen-based therapeutic vaccine has achieved high response rate in the clinical trials rising the immunotherapy as a promising alternative for colorectal cancer. Herein, colon cancer cells derived neoantigen peptide Adpgk were employed to be co-encapsulated with black phosphorus quantum dots into liposome (Adpgk-BPQDs-liposome) as therapeutic vaccine. Adpgk-BPQDs-liposome were dispersed in F127 gel containing GM-CSF. The heat generated by black phosphorus (BP) under 808 nm near-infrared laser irradiation accelerates the F127 gel ablation and the release of GM-CSF, which recruit APC cells and prime the native T cells. The tumor bearing mice received the programmed cell death protein 1 (PD-1) checkpoint blockade antibody combined with photo-thermal gel intensively prevented the tumor progress. Furthermore, the tumor infiltrating CD8+ T cells were significantly increased which lead to the elimination of the tumor.

Surgical Tumor-Derived Personalized Photothermal Vaccine Formulation for Cancer Immunotherapy.

Personalized cancer vaccines show great potential in cancer immunotherapy by inducing an effective and durable antitumor response. However, the limitation of neoantigen identification, low immunogenicity, and weak immune response hamper the development of personalized cancer vaccines. The surgically removed tumor contains tumor antigens specific to the patient, which provides a promising source for personalized cancer vaccines. Here, we utilized the surgically removed tumor to prepare a personalized photothermal vaccine combined with the PD-1 checkpoint blockade antibody to prevent tumor relapse and metastasis. Black phosphorus quantum dot nanovesicles (BPQD-CCNVs) coated with surgically removed tumor cell membrane were prepared and loaded into a thermosensitive hydrogel containing GM-CSF and LPS. The sustained release of GM-CSF from the hypodermic injection of Gel-BPQD-CCNVs effectively recruited dendritic cells to capture tumor antigen. NIR irradiation and LPS stimulated the expansion and activation of DCs, which then traveled to the lymph nodes to present antigen to CD8+ T cells. Moreover, the combination with PD-1 antibody significantly enhanced tumor-specific CD8+ T cell elimination of the surgical residual and lung metastatic tumor. Hence, our work may provide a promising strategy for the clinical development of a personalized cancer vaccine.

Photothermal cancer immunotherapy by erythrocyte membrane-coated black phosphorus formulation.

Basal-like breast cancer exhibits a triple-negative phenotype and has a poor prognosis, even with traditional chemical and anti-human epidermal growth factor receptor (HER) treatments. However, the high mutation rate of this obstinate cancer type renders it suitable for immunotherapy. Photothermal therapy (PTT) is a high-efficiency method for inducing tumor neoantigen release in situ, which has great potential for use in cancer immunotherapy. Here, we prepared a biomimetic black phosphorus quantum dot (BPQDs) formulation to induce breast cancer cell apoptosis in situ by near-infrared (NIR) laser irradiation to mobilize the immune system to eliminate the residual and metastatic cancer cells. Erythrocyte membranes (RMs) were used to coat the BPQDs, forming a BPQD-RM nanovesicle (BPQD-RMNV) biomimetic formulation that exhibited a long circulation time and tumor accumulation in vivo. The basal-like 4T1 breast tumor underwent apoptosis and necrosis with the irradiation and recruited dendritic cells (DCs) to capture the tumor antigens in vivo. Furthermore, programmed cell death protein 1 (PD-1) antibody (aPD-1) was employed to prevent the CD8+ T cells from exhaustion. Notably, BPQD-RMNV-mediated PTT combined with aPD-1 treatment significantly delayed residual and metastatic tumor growth in vivo. Hence, BPQD-RMNV-mediated PTT combined with immune checkpoint blockade antibody increased the infiltration and activity of CD8+ T cells in the tumor, which directly restrained basal-like breast tumor growth in vivo.