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Summary: Immunogenic cell death (ICD) is a unique mode of cell death, which can release immunogenic damage‐associated molecular patterns (DAMPs) and tumor‐associated antigens to trigger long‐term protective antitumor immune responses. Thus, amplifying "eat me signal" during tumor ICD cascade is critical for cancer immunotherapy. Some therapies (radiotherapy, photodynamic therapy (PDT), photothermal therapy (PTT), etc.) and inducers (chemotherapeutic agents, etc.) have enabled to initiate and/or facilitate ICD and activate antitumor immune responses. Recently, nanostructure‐based drug delivery systems have been synthesized for inducing ICD through combining treatment of chemotherapeutic agents, photosensitizers for PDT, photothermal transformation agents for PTT, radiosensitizers for radiotherapy, etc., which can release loaded agents at an appropriate dosage in the designated place at the appropriate time, contributing to higher efficiency and lower toxicity. Also, immunotherapeutic agents in combination with nanostructure‐based drug delivery systems can produce synergetic antitumor effects, thus potentiating immunotherapy. Overall, our review outlines the emerging ICD inducers, and nanostructure drug delivery systems loading diverse agents to evoke ICD through chemoradiotherapy, PDT, and PTT or combining immunotherapeutic agents. Moreover, we discuss the prospects and challenges of harnessing ICD induction‐based immunotherapy, and highlight the significance of multidisciplinary and interprofessional collaboration to promote the optimal translation of this treatment strategy. [ABSTRACT FROM AUTHOR]

The construction of C−N bonds is considered one of the most useful reactions in synthetic chemistry due to their widespread presence in pharmaceuticals, natural products, etc. Pd‐catalyzed Buchwald–Hartwig amination (BHA) has provided the most efficient method to form (hetero)aryl amines but it required strong base and sophisticated ligands. In comparison, the combination of photocatalysis and nickel chemistry has revolutionized catalytic strategies and is emerging as a quintessence to realize BHA, termed as Ni‐metallaphotoredox BHA. To pursue a universal protocol, diverse photocatalysts were designed and employed in Ni‐metallaphotoredox BHA, and smoothly promoted C−N bond formations under irradiation of light from ultraviolet to red light, respectively. Note that the matching of photocatalyst and light was critical for success. Therefore, this review mainly focuses on the discussion of Ni‐metallaphotoredox BHA according to the irradiation light's wavelength, covering ultraviolet, purple, blue, red, and white light as well as solar light. We try to find a clue in the relationship of structure‐photophysical behaviors of photocatalysts under the same or different irradiation light. At last, current limitations and potential trends for advancing Ni‐metallaphotoredox BHA are highlighted. We deem that it could encourage chemists to continue designing suitable photocatalyst for C−N bond formations under sunlight mimicking plants' photosynthesis. [ABSTRACT FROM AUTHOR]

Highlights Polyurethane has been widely studied as a lightweight reinforcing material. This paper uses two types of hollow glass microspheres to modify polyurethane in different proportions to prepare a variety of lightweight cores for reinforcing carbon fiber tubes. A quasi‐static lateral compression test was performed on the reinforced carbon fiber tube to analyze the effect of reinforcement materials on mechanical properties, failure modes and crashworthiness. The results show that BR20 reinforcement material has the best effect on enhancing the mechanical properties and crashworthiness of the structure, and its energy absorption is 3.5 times higher than that of carbon fiber tubes. Hollow glass microspheres can improve the reinforcing effect of polyurethane. Lightweight cores prepared from different types of hollow glass microspheres show different failure modes during lateral compression (polyurethane and BR60 show better ductility, and BR20 shows shear failure). The BR20 and BR60 are mixed in different proportions, the reinforced polyurethane foam reinforced carbon fiber tube can have little difference in the energy absorption. The addition of BR20 and BR60 showed a large difference in the force‐displacement curve during the compression stage. A qualitative analysis is conducted based on the effect of the total energy absorption of the structure on the reinforcement materials. The lightweight core is prepared by hollow glass microspheres and polyurethane. Reinforcement materials enhance the lateral compression performance. Reinforcement materials enhance the crashworthiness performance. Reinforcement materials affect failure modes. The proportion of BR20 and BR60 affects the performance of the lightweight core. [ABSTRACT FROM AUTHOR]

Loss of refreshment in nucleus pulposus (NP) cellularity leads to intervertebral disc (IVD) degeneration. Nevertheless, the cellular sequence of NP cell differentiation remains unclear, although an increasing body of literature has identified markers of NP progenitor cells (NPPCs). Notably, due to their fragility, the physical enrichment of NP‐derived cells has limited conventional transcriptomic approaches in multiple studies. To overcome this limitation, a spatially resolved transcriptional atlas of the mouse IVD is generated via the 10x Genomics Visium platform dividing NP spots into two clusters. Based on this, most reported NPPC‐markers, including Cathepsin K (Ctsk), are rare and predominantly located within the NP‐outer subset. Cell lineage tracing further evidence that a small number of Ctsk‐expressing cells generate the entire adult NP tissue. In contrast, Tie2, which has long suggested labeling NPPCs, is actually neither expressed in NP subsets nor labels NPPCs and their descendants in mouse models; consistent with this, an in situ sequencing (ISS) analysis validated the absence of Tie2 in NP tissue. Similarly, no Tie2‐cre‐mediated labeling of NPPCs is observed in an IVD degenerative mouse model. Altogether, in this study, the first spatial transcriptomic map of the IVD is established, thereby providing a public resource for bone biology. [ABSTRACT FROM AUTHOR]