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Diffuse intrinsic pontine glioma (DIPG) is a highly lethal tumor that occurs in the brain stem. At present, there is no effective drug for DIPG. In this work, Na/K‐ATPase inhibitor‐ouabain (OB) is found to efficiently kill H3K27M‐mutated DIPG at low doses, inhibit tumor cell proliferation, reduce tumor stemness for the first time, demonstrating its potential as a chemotherapy drug for DIPG. In order to increase the blood–brain barrier (BBB) permeability and tumor accumulation of OB, acidic‐responsive engineered exosomes loaded with OB (OB@EXO‐LCCP) are constructed, which increase the accumulation of OB within the tumor microenvironment of DIPG and efficiently deliver OB to DIPG cells to achieve targeted killing effect. In in vitro experiments, OB@EXO‐LCCP is able to release OB in an acid‐responsive manner and effectively kill DIPG tumor cells. In in vivo experiments, OB@EXO‐LCCP significantly inhibits DIPG growth and prolongs the overall survival of DIPG‐bearing mice. Overall, OB@EXO‐LCCP can promote the BBB permeability and tumor‐targeting ability of OB, thereby enhancing its DIPG‐killing ability and reducing its toxicity. This study provides technical and theoretical information for the precision therapy of DIPG. [ABSTRACT FROM AUTHOR]

The importance of oospores in the ecology and life cycle of annual charophyte species is now widely recognized. To elucidate the primary factor that determines the timing (onset) of sexual reproduction, a controlled 3 × 2 factorial experiment with various light levels (100%, 50% and 10% of natural irradiance) and temperatures (25 °C and 20 °C) was conducted to assess their interactive effects on Chara braunii Gmelin under greenhouse conditions. Results revealed that when the light level decreased from 100% to 10% of natural irradiance, the occurrence of gametangia was postponed for 8 days and the proportions of branch whorls with gametangia (PG) and oospores (PO) significantly decreased under high-temperature conditions. Decreased temperature significantly delayed the emergence of gametangia (100% of light levels for 10 days, 50% of light level for 6 days) and decreased PG and PO. Under low-temperature conditions, no gametangia were found at the lowest light level (10/20). This indicated that the combination of low light and low temperature could result in the absence of sexual reproduction in C. braunii. Furthermore, the internode length, dry weight length ratio and pigment pattern of cultured C. braunii were also significantly altered in response to different light levels and temperature treatments. Two-way ANOVA analysis revealed that temperature contributed more to PG and PO than light levels, while light levels contributed more to morphology and pigment ratio than temperature. This might suggest distinct responses of sexual reproduction onset and growth of C. braunii to varied light level and temperature. [ABSTRACT FROM AUTHOR]