Maize (Zea mays L.) is highly sensitive to drought stress, resulting in large losses in yield; therefore, strategies aimed at enhancing drought tolerance are essential. Melatonin improves stress tolerance in plants; however, its mechanism in maize seedlings under drought stress remains unknown. Therefore, we investigated the effects of foliar-sprayed melatonin (100 umol L−1) on the antioxidant system, photosynthetic gas exchange parameters, stomatal behavior, endogenous melatonin and abscisic acid (ABA)-related gene expression in maize seedling leaves under 20% polyethylene glycol (PEG)-induced drought stress. PEG treatment resulted in oxidative stress and stomatal closure, resulting in chlorophyll degradation and inhibition of photosynthesis; thereby, reducing seedling biomass. Melatonin pretreatment significantly improved the relative water content, photosynthetic gas exchange parameters and stomatal behavior; thereby, maintaining chlorophyll contents and photosynthesis. Melatonin also stimulated the antioxidant system, enhancing the clearance of reactive-oxygen species, preventing severe damage under PEG-induced drought. Pre-treatment also increased endogenous melatonin and inhibited up-regulation of NCED1, an ABA synthesis-related gene, as well as selectively up-regulating ABA catabolic genes ABA8ox1 and ABA8ox3, reducing ABA accumulation and inducing stomatal reopening. Overall, these findings suggest that melatonin pre-treatment alleviated the inhibitory effects of drought stress on photosynthesis, enhancing tolerance in maize seedlings.
Phytohormones are a class of small organic molecules that are widely used in higher plants and microalgae as chemical messengers. Phytohormones play a regulatory role in the physiological metabolism of cells, including promoting cell division, increasing stress tolerance, and improving photosynthetic efficiency, and thereby increasing biomass, oil, chlorophyll, and protein content. However, traditional abiotic stress methods for inducing the accumulation of energy storage substances in microalgae, such as high light intensity, high salinity, and heavy metals, will affect the growth of microalgae and will ultimately limit the efficient accumulation of energy storage substances. Therefore, the addition of phytohormones not only helps to reduce production costs but also improves the efficiency of biofuel utilization. However, accurate and sensitive phytohormones determination and analytical methods are the basis for plant hormone research. In this study, the characteristics of phytohormones in microalgae and research progress for regulating the accumulation of energy storage substances in microalgae by exogenous phytohormones, combined with abiotic stress conditions at home and abroad, are summarized. The possible metabolic mechanism of phytohormones in microalgae is discussed, and possible future research directions are put forward, which provide a theoretical basis for the application of phytohormones in microalgae.
Meniere’s disease (MD) is a disorder of the inner ear characterized by episodes of spontaneous vertigo, fluctuating hearing loss, and tinnitus. Recent studies have demonstrated that IgE may play a role in the pathogenesis of MD. Patients with MD (n = 103), acoustic neuroma (n = 5), and healthy subjects (n = 72) were recruited into the study. Serum from the participants was analyzed for IgE and type 2–related cytokines. IgE and CD23 expression levels in vestibular end organs of patients, C57BL/6 mice, or mouse HEI-OC1 cells were analyzed. Finally, the role of CD23 in IgE transcytosis was assessed using HEI-OC1 cells. Serum IgE was elevated in patients with MD and positively correlated with clinical symptoms. IL-4, IL-5, IL-10, IL-13, and CD23 levels were increased in patients with MD compared with the control group. In the transcytosis assay, mouse IgE was found to be bidirectionally transported across the HEI-OC1 cell monolayer. Additionally, CD23 downregulation using a small interfering RNA approach significantly reduced the efficiency of IgE transcytosis, suggesting that IgE is transported by CD23. Furthermore, exposure to IL-4 increased CD23 expression and enhanced IgE transcytosis in the HEI-OC1 cells and primary vestibular end organs. Our study indicated that IgE may play a role in the pathophysiology of MD. In addition, CD23-mediated IgE transcytosis in the hair cells may play a critical role in initiating inflammation in the inner ear. Thus, reducing the level of IgE may be a potentially effective approach for MD treatment.
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