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Soil salinization, a growing problem in arid and semi-arid areas, significantly influences the ecological dynamics and processes in wetland ecosystems. To fully examine the physiological responses with the aim of wetland protection and management, a laboratory simulation experiment was conducted to study the effects of soil salinization on the growth of C. schmidtii tussocks. Plant height and leaf traits, as well as physiological characteristics, were analyzed to explore the responses of C. schmidtii to soil salinization. Results showed that the highest value of electrical conductivity (EC) (4.71 mS/cm) recorded in 4000 mg/L treatment was 3.04 times greater than the lowest value (1.55 mS/cm) recorded in 0 mg/L treatment. It was well demonstrated that plant height under the 1000 mg/L treatment was 57.6% greater than that obtained under the 4000 mg/L treatment. Additionally, the growth of plants under the 4000 mg/L treatment achieved significantly higher length and the ratio of leaf withering (by 13.76 and 16.42 times, respectively), compared with those obtained under 0 mg/L treatment. 0 and 1000 mg/L treatments were found to greatly increase chlorophyll content and decrease malondialdehyde. Hence, slight salinization will stimulate the responses of C. schmidtii to environmental fluctuation, but the persistent serious salinization can inhibit the growth and physiology of C. schmidtii. The optimum ecological threshold of salinity for the growth of C. schmidtii was in the range 0~1000 mg/L. Results help in understanding the responses of C. schmidtii tussocks to soil salinization, and suggest the vital significance of preventing salinization in the Momoge Wetlands of northeastern China.
Bone morphogenetic proteins (BMPs), a subgroup of the TGF-P superfamily, play critical roles in neural progenitor cell fate determination. Neural stem cells (NSCs) are multipotent progenitor cells that can differentiate into neurons, oligodendrocytes and astrocytes under certain conditions. In our recent report, using an antibody that can recognize both BMP-2 and BMP-4 (BMP-2/4), we showed that BMP-2/4 is only expressed in astrocytes differentiated from NSCs in a medium containing 1% fetal bovine serum (FBS). In this in vitro model, the astrocytic differentiation of NSCs was mainly toward type-2. When NSCs were cultured in a medium containing 10% FBS, most of the cells differentiated into type-1 astrocytes. However, little information is available for BMP-2 and BMP-4 expression in type-1 and type-2 astrocytes induced from NSCs under these different culture conditions. In this study, using two antibodies specific for BMP-2 and BMP-4, respectively, we discriminated the presence of BMP-2 and BMP-4 in NSCs and their derivatives under 1% and 10% FBS culture conditions by RT-PCR, western blot and immunofluorescence staining. We found that BMP-2 and BMP-4 are highly expressed in both type-1 and type-2 astrocytes, and no detectable expression in NSCs, neurons and oligodendrocytes. This suggests that the astrocytes might be one source of BMPs during the differentiation of NSCs. However, in our model, we cannot exclude the possibility that microglia or endothelial cells could also be a source of BMPs.
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