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The present study estimated the biodistribution and radiationabsorbed dose of epidermal growth factor receptor (EGFR) radioligand 11 C-PD153035 in whole-body PET examinations of healthy volunteers. Methods: Two-dimensional whole-body PET was performed on 9 subjects after injection of 11 C-PD153035 at 329.3 6 77.8 MBq (mean 6 SD). A total of 12 frames were acquired for approximately 90 min in 7 segments of the body. Regions of interest were drawn on PET images of source organs. Residence time was calculated as the area under the timeactivity curve. Radiation dosimetry was calculated from organ residence time by use of MIRDOSE3 software. Results: The renal and hepatobiliary systems played important roles in 11 C-PD153035 excretion from the body, accounting for the excretion of approximately 23% and 19% of the injected radioactivity, respectively. Blood-pool activity was only moderate and declined over time. Tracer accumulation in the lungs, bone marrow, and muscles was slight, resulting in low background activity in the chest. The organs with the highest radiation-absorbed doses were the urinary bladder and the gallbladder; the effective doses were 6.08E202 6 1.85E202 and 2.40E202 6 8.01E203 mGy/ MBq, respectively. The effective dose equivalent was 7.43E203 6 1.10E203 mSv/MBq, and the dose-limiting organ was the urinary bladder. Conclusion: On the basis of the estimated absorbed dose, 11 C-PD153035 displayed a favorable radiation dose profile in humans and therefore could be used in multiple PET examinations of the same subject per year. 11 C-PD153035 is a promising ligand for the investigation of EGFR in humans, especially in chest tumors such as non-small cell lung cancer.

1) U-2 OS cells express IGF-I and IGF-II/M6P receptors. 2) U-2 OS tumor cells respond to the addition of exogenous IGF-I and IGF-II with an increase of DNA synthesis.(ABSTRACT TRUNCATED AT 400 WORDS)

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Guard cell walls of stomata are highly specialized in plants. Previous research focused on the structure and anatomy of guard cell walls, but little is known about guard cell regulation during stomata movement. In this work, we investigate the possible biological role of the Arabidopsis expansin gene AtEXPA1 in stomatal opening. The AtEXPA1 promoter drove the expression of the GUS reporter gene specifically in guard cells. Light-induced stomatal opening was accelerated in 35S::AtEXPA1 lines, whereas the anti-AtEXPA1 antibody decelerated light-induced stomatal opening. The inhibition of the anti-AtEXPA1 antibody on stomatal opening was largely dependent on the environmental pH. The volumetric elastic modulus (ε) was measured as an indicator of changes in the cell wall. The ε value of guard cells in 35S::AtEXPA1 lines was smaller than in the wild types. The putative role of AtEXPA1 as controller of stomatal opening rate and its regulation are discussed.

Soil gross nitrogen (N) transformations are crucial for assessing forest N status. Although there is evidence suggesting that the N cycle is open in the karst forest, southwest China, process‐based investigation of gross soil N transformations is limited. In the current study, gross soil N transformations were investigated using 15N isotope dilution and 15N tracer techniques in a typical karst forest with calcareous soil (Calcareous lithosols) in comparison with an adjacent nonkarst forest with red soil (Haplic acrisol).The gross rates of N mineralization, nitrification, dissimilatory nitrate reduction to ammonium (DNRA), and nitrate immobilization were significantly greater in the karst forest. Ammonium immobilization was comparable to gross N mineralization, so that ammonium could be efficiently conserved in the nonkarst forest. Meanwhile, the produced nitrate was mostly retained via DNRA and nitrate immobilization. This resulted in a negligible net nitrate production in the nonkarst forest. In contrast, ammonium immobilization rate only accounted for half of gross N mineralization rate in the karst forest. The nitrate retention capacity is relatively low, with 41.6 ± 4.2% of the produced nitrate being retained via DNRA and nitrate immobilization. Due to relatively low nitrate retention capacity, nitrate was accumulated in the karst forest soil. Our results indicate that the nonkarst forest with red soil holds a very conservative N cycle, but the N cycle in the karst forest is leaky.

A high-density SNP map was constructed and several novel QTL for branch angle across six environments in Brassica napus were identified. Branch angle is a major determinant for the ideotype of a plant, while the mechanisms underlying this trait in Brassica napus remain elusive. Herein, we developed one doubled haploid population from a cross involving one Capsella bursa-pastoris derived B. napus intertribal introgression line with the compressed branches and wooden stems, and constructed a high-density SNP map covering the genetic distance of 2242.14 cM, with an average marker interval of 0.73 cM. After phenotypic measurements across six environments, the inclusive composite interval mapping algorithm was conducted to analyze the QTL associated with branch angle. In single-environment analysis, a total of 17 QTL were detected and mainly distributed on chromosomes A01, A03, A09 and C03. Of these, three major QTL, qBA.A03-2, qBA.C03-3 and qBA.C03-4 were steadily expressed, each explaining more than 10% of the phenotypic variation in at least two environments. Compared with other results on rapeseed branch angle, these major QTL were newly detected. In QTL by environment interactions (QEI) mapping, 10 QTL were identified, and the QTL average effect and QEI effect were estimated. Of these, 7 QTL were detected in both single-environment analysis and QEI mapping. Based on the physical positions of SNPs and the functional annotation of the Arabidopsis thaliana genome, 27 genes within the QTL regions were selected as candidate genes, including early auxin-responsive genes, small auxin-up RNA, auxin/indoleacetic acid and gretchenhagen-3. These results may pave the way for deciphering the genetic control of branch angle in B. napus.