Search

• The current work identified that platelets could be activated by photodynamic and photothermal effects (PDE/PTE). • The activated platelets release growth factor, potentiating wound repair in a laser-controlled manner. • This work provides a promising approach for mediating wound repair controllably and the application of cytopharmaceutics. Prompt and effective wound repair is an essential strategy to promote recovery and prevent infection in patients with various types of trauma. Platelets can release a variety of growth factors upon activation to facilitate revascularization and tissue repair, provided that their activation is uncontrollable. The present study is designed to explore the selective activation of platelets by photodynamic and photothermal effects (PDE/PTE) as well as the trauma repair mediated by PDE/PTE. In the current research, platelets were extracted from the blood of mice. Indocyanine green (ICG) was applied to induce PDE/PTE. The uptake of ICG by platelets was detected by laser confocal microscopy and flow cytometry. The cellular integrity was measured by microscopy. The reactive oxygen species (ROS) generation and temperature of platelets were assayed by 2,7-Dichlorodihydrofluorescein diacetate (DCFH-DA) and temperature detector. The activation of platelets was measured by western blots (WB), dynamic light scattering (DLS), and scanning electron microscopy (SEM). The release of growth factor was detected by enzyme-linked immuno sorbent assay (Elisa), wherein the in vitro cell proliferation was investigated by 5-Ethynyl-2'-deoxyuridine (EDU) assay. The wound infection rates model and histological examination were constructed to assay the ICG-loaded platelet-mediated wound repair. Platelets could load with ICG, a kind of photodynamic and photothermal agent, as carriers and remain intact. Near-infrared (NIR) laser irradiation of ICG-loaded platelets (ICG@PLT) facilitated higher temperature and ROS generation, which immediately activated ICG@PLT, as characterized by increased membrane p-selectin (CD62p), cyclooxygenase-2 (COX-2), thromboxane A2 receptor (TXA2R) expression, elevated hydrated particle size, and prominent aggregation in platelets. Further investigation revealed that massive insulin-like growth factor (IGF) and platelet-derived growth factor (PDGF) were released from the activated ICG@PLT, which also promoted the proliferation of endothelial cells and keratinocytes in co-culture. In consequence, activated platelets and increased neovascularization could be observed in rats with wound infection treated by ICG@PLT in the presence of NIR. More impressively, the hydrogel containing ICG@PLT accelerated wound healing and suppressed inflammation under NIR, exhibiting excellent wound repair properties. Taken together, the current work identified that platelets could be activated by PDE/PTE and thereby release growth factor, potentiating wound repair in a controlled manner. [Display omitted] [ABSTRACT FROM AUTHOR]

In this study, aiming to optimize the multi-workflow scheduling order, in which tasks submitted at different time require different service quality, we present a fair multi-workflow scheduling scheme based on reinforcement learning. Firstly we design a dynamic priority-driven algorithm, in order to set the initial state of the task priority according to the type of cloud workflow and service quality on the one hand, and on the other hand, to adjust the tasks priority dynamically while scheduling so as to avoid violating the Service Level Agreement by delaying the workflow provisioning. Secondly, we design a fine-grained cloud computing model and apply the reinforcement-learning based scheduling algorithm to balance the cluster loads. Finally the experimental results prove the effectiveness of this scheme. [ABSTRACT FROM AUTHOR]

The immunosuppressive microenvironment of lung cancer serves as an important endogenous contributor to treatment failure. The present study aimed to demonstrate the promotive effect of DHA on immunogenic cell death (ICD) in lung cancer as well as the mechanism. The lewis lung cancer cells (LLC), A549 cells and LLC-bearing mice were applied as the lung cancer model. The apoptosis, ferroptosis assay, western blotting, immunofluorescent staining, qPCR, comet assay, flow cytometry, confocal microscopy, transmission electron microscopy and immunohistochemistry were conducted to analyze the functions and the underlying mechanism. An increased apoptosis rate and immunogenicity were detected in DHA-treated LLC and tumor grafts. Further findings showed DHA caused lipid peroxide (LPO) accumulation, thereby initiating ferroptosis. DHA stimulated cellular endoplasmic reticulum (ER) stress and DNA damage simultaneously. However, the ER stress and DNA damage induced by DHA could be abolished by ferroptosis inhibitors, whose immunogenicity enhancement was synchronously attenuated. In contrast, the addition of exogenous iron ions further improved the immunogenicity induced by DHA accompanied by enhanced ER stress and DNA damage. The enhanced immunogenicity could be abated by ER stress and DNA damage inhibitors as well. Finally, DHA activated immunocytes and exhibited excellent anti-cancer efficacy in LLC-bearing mice. In summary, the current study demonstrates that DHA triggers ferroptosis, facilitating the ICD of lung cancer thereupon. This work reveals for the first time the effect and underlying mechanism by which DHA induces ICD of cancer cells, providing novel insights into the regulation of the immune microenvironment for cancer immunotherapy by Chinese medicine phytopharmaceuticals. [Display omitted] [ABSTRACT FROM AUTHOR]

Broomella and Hyalotiella are poorly known genera in Amphisphaeriaceae . Both genera are known from morphological descriptions, but lack molecular data, thus their generic placement and relationships with other genera are unclear. Three collections of Amphisphaeriaceae were made from dead twigs of Clematis in Italy, and two from Spartium species and were identified as Broomella and Hyalotiella species. In order to obtain a phylogenetic understanding of Broomella and Hyalotiella within the family Amphisphaeriaceae , we carried out a phylogenetic analysis based on LSU gene data. Results show that these five isolates represent two distinct genera. Based on both morphological and phylogenetic data, the three isolates form Clematis are shown to be conspecific with Broomella vitalbae . In this paper we designated an epitype with a sexual and asexual morph for B. vitalbae to stabilize the understanding of the genus. The two strains from Spartium fit within the generic concepts of Hyalotiella , but sequence data for Hyalotiella species are presently lacking. Hyalotiella spartii sp. nov. is introduced based on its host association and morphological characters. [ABSTRACT FROM AUTHOR]

Vamsapriya comprises two species from bamboo and is characterized by erect, rigid, dark brown, synnematous conidiophores, monotretic conidiogenous cells and brown to dark brown, septate, conidia in chains. Vamsapriya indica, the generic type of Vamsapriya, was recollected and isolated from bamboo culms in Chiang Rai Province, Thailand and is described, illustrated and epitypified in this paper. Two new species in the genus were also discovered and are introduced as V. khunkonensis and V. bambusicola. The new species differs from the type and the other known species, V. mahabaleshwarensis, in the shape and size of the conidia. Maximum-parsimony (MP) analysis of combined LSU, SSU and RPB2 sequence data and Bayesian analysis based on multi-gene data set of betatubulin, ITS, LSU, and RPB2 show Vamsapriya belongs in Xylariaceae, Xylariales. [ABSTRACT FROM AUTHOR]

• Ce6 mediated PDT could induce obvious DNA damage and activate ATM-related DNA damage response (DDR) through generation of ROS in a short period time. • ATM inhibitor could ameliorate the efficacy of Ce6-triggered PDT for lung cancer by blocking the DDR. • The present study reveals a novel resistance mechanism of PDT and proposes an intervention strategy by the use of ATM inhibitor. Photodynamic therapy (PDT) is a promising strategy for the treatment of malignant tumors due to its high selectivity, limited-toxicity, and non-invasiveness. However, PDT can also induce DNA damage and subsequent repair response, which may reduce the efficacy of PDT. In the present study, we sought to explore the effect of chlorin e6 (Ce6)-mediated PDT on DNA damage and DNA damage response (DDR) in lung cancer cells. In addition, the effect of PDT combined with ATM inhibitor on molecules of DDR and the possibility of improving the efficacy of PDT were further investigated. In the in vitro study, lewis cells were submitted to Ce6 treatment (2, 4, 8, 16, 32 μg/mL). To determine the concentration of Ce6, uptake and toxicity of Ce6 mediated PDT were detected using flow cytometry (FACS), Confocal microscopy, and CCK-8. In the subsequent research, 8 μg/mL of Ce6 was the treatment condition for inducing PDT. The different post-irradiation placement times were further grouped under this condition (2, 4, 6, 12 h). Cellular reactive oxygen species (ROS), damage of DNA were measured by DCFH-DA probe, comet assay respectively. Then the expression of p-ATM, p53, and γ-H2A.X proteins related to DNA damage response, was detected by WB. The efficacy of Ce6 induced PDT was also demonstrated by Annexin-V/PI staining as well as the expression of PCNA, cleaved-caspase-3. On this basis, ATM inhibitor was applied to treat lewis cells combined with Ce6 (2, 4 h) to investigate whether the efficacy of PDT induced by Ce6 can be improved after the ATM-related DDR was blocked. The cell viability, apoptosis, and expression of associated proteins were assayed. At 2–4 h after PDT treatment, ROS was dramatically elevated in lewis cells, DNA double-strand breaks (DDSB) occurred, as well as up-regulation of DDR proteins γ-H2A.X, p-ATM, and p53. At the same time, lewis cells did not undergo significant apoptosis. After ATM inhibition, the DDR was significantly blocked within 2–4 h after Ce6 induced PDT, along with a pronounced decrease in cell viability followed by a prominent increase of apoptosis. Ce6-mediated PDT generates ROS in a short period time, thus inducing DNA damage, ATM-related DDR as well as promoting resistance of lung cancer cells to PDT. Combining ATM inhibitor with PDT could effectively inhibit the DDR induced by PDT, thereby enhancing the efficacy. This study reveals a new resistance mechanism of PDT and proposes an intervention strategy. [ABSTRACT FROM AUTHOR]