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| 3. |
- Belitsky, Victor, 1955, et al.
(författare)
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A new 3 mm band receiver for the Onsala 20 m antenna
- 2015
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Ingår i: Astronomy and Astrophysics. - : EDP Sciences. - 0004-6361 .- 1432-0746. ; 580
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Tidskriftsartikel (refereegranskat)abstract
- A new receiver for the Onsala 20 m antenna with the possibility of being equipped with 3 mm and 4 mm bands has been built and the 3 mm channel has been commissioned during the Spring 2014. For single-dish operation, the receiver uses an innovative on-source/off-source optical switch. In combination with additional optical components and within the same optical layout, the switch provides two calibration loads (for the 3 mm and 4 mm channels), sideband rejection measurement, and tuning possibilities. The optical layout of the receiver employs all cold (4 K) offset elliptical mirrors for both channels, whereas the on-off switch employs flat mirrors only. The 3 mm channel employs a sideband separation (2SB) dual polarization receiver with orthomode transducer (OMT), 4-8 GHz intermediate frequency (IF), x? 2pol x? upper and lower sidebands (USB? +? LSB). The cryostat has four optical windows made of high density polyethylene (HDPE) with anti-reflection corrugations, two for the signal and two for each frequency band cold load. The cryostat uses a two-stage cryocooler produced by Sumitomo HI? RDK? 408D2 with anti-vibration suspension of the cold-head to minimize impact of the vibrations on the receiver stability. The local oscillator (LO) system is based on a Gunn oscillator with aphase lock loop (PLL) and four mechanical tuners for broadband operation, providing independently tunable LO power for each polarization. This paper provides a technical description of the receiver and its technology and could be useful for instrumentation engineers and observers using the Onsala 20 m telescope.
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- He, Fei, et al.
(författare)
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FPR2 Shapes an Immune-Excluded Pancreatic Tumor Microenvironment and Drives T-cell Exhaustion in a Sex-Dependent Manner
- 2023
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Ingår i: Cancer Research. - : American Association for Cancer Research (AACR). - 0008-5472 .- 1538-7445. ; 83:10, s. 1628-1645
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Tidskriftsartikel (refereegranskat)abstract
- Sex-driven immune differences can affect tumor progression and the landscape of the tumor microenvironment. Deeper understanding of these differences in males and females can inform patient selection to improve sex-optimized immunotherapy treatments. In this study, single-cell RNA sequencing and protein analyses uncovered a subpopulation of myeloid cells in pancreatic lesions associated with an immune-excluded tumor phenotype and effector T-cell exhaustion exclusively in females. This myeloid subpopulation was positively correlated with poor survival and genetic signatures of M2-like macrophages and T-cell exhaustion in females. The G-protein coupled receptor formyl peptide receptor 2 (FPR2) mediated these immunosuppressive effects. In vitro, treatment of myeloid cells with a specific FPR2 antagonist prevented exhaustion and enhanced cytotoxicity of effector cells. Proteomic analysis revealed high expression of immunosuppressive secretory proteins PGE2 and galectin-9, enriched integrin pathway, and reduced proinflammatory signals like TNFα and IFNγ in female M2-like macrophages upon FPR2 agonist treatment. In addition, myeloid cells treated with FPR2 agonists induced TIM3 and PD-1 expression only in female T cells. Treatment with anti-TIM3 antibodies reversed T-cell exhaustion and stimulated their ability to infiltrate and kill pancreatic spheroids. In vivo, progression of syngeneic pancreatic tumors was significantly suppressed in FPR2 knockout (KO) female mice compared with wild-type (WT) female mice and to WT and FPR2 KO male mice. In female mice, inoculation of tumors with FPR2 KO macrophages significantly reduced tumor growth compared with WT macrophages. Overall, this study identified an immunosuppressive function of FPR2 in females, highlighting a potential sex-specific precision immunotherapy strategy.
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- Aabel, Lise, et al.
(författare)
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A TDD Distributed MIMO Testbed Using a 1-bit Radio-Over-Fiber Fronthaul Architecture
- 2024
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Ingår i: IEEE Transactions on Microwave Theory and Techniques. - 0018-9480 .- 1557-9670. ; In Press
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Tidskriftsartikel (refereegranskat)abstract
- We present the uplink and downlink of a time-division duplex distributed multiple-input multiple-output (D-MIMO) testbed, based on a 1-bit radio-over-fiber architecture, which is low cost and scalable. The proposed architecture involves a central unit (CU) that is equipped with 1-bit digital-to-analog and analog-to-digital converters, operating at 10 GS/s. The CU is connected to multiple single-antenna remote radio heads (RRHs) via optical fibers, over which a binary radio frequency (RF) waveform is transmitted. In the uplink, a binary RF waveform is generated at the RRHs by a comparator, whose inputs are the received RF signal and a suitably designed dither signal. In the downlink, a binary RF waveform is generated at the CU via bandpass sigma-delta modulation. Our measurement results show that low error-vector magnitude (EVM) can be achieved in both the uplink and the downlink, despite 1-bit sampling at the CU. Specifically, for point-to-point over-cable transmission between a single user equipment (UE) and a CU equipped with a single RRH, we report, for a 10-MBd signal using single-carrier (SC) 16 quadratic-amplitude modulation (QAM) modulation, an EVM of 3.3% in the downlink, and of 4.5% in the uplink. We then consider a CU connected to three RRHs serving over the air two UEs, and show that, after over-the-air reciprocity calibration, a downlink zero-forcing precoder designed on the basis of uplink channel estimates at the CU achieves an EVM of 6.4% and 10.9% at UE 1 and UE 2, respectively. Finally, we investigate the ability of the proposed architecture to support orthogonal frequency-division multiplexing (OFDM) waveforms, and its robustness against both in-band and out-of-band interference.
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- Agrawal, Piyush, et al.
(författare)
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Long Term Channel Characterization for Energy Efficient Transmission in Industrial Environments
- 2014
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Ingår i: IEEE Transactions on Communications. - 0090-6778 .- 1558-0857. ; 62:8, s. 3004-3014
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Tidskriftsartikel (refereegranskat)abstract
- One of the challenges for a successful use of wireless sensor networks in process industries is to design networks with energy efficient transmission, to increase the lifetime of the deployed network while maintaining the required latency and bit-error rate. The design of such transmission schemes depend on the radio channel characteristics of the region. This paper presents an investigation of the statistical properties of the radio channel in a typical process industry, particularly when the network is meant to be deployed for a long time duration, e. g., days, weeks, and even months. Using 17-20-h-long extensive measurement campaigns in a rolling mill and a paper mill, we highlight the non-stationarity in the environment and quantify the ability of various distributions, given in the literature, to describe the variations on the links. Finally, we analyze the design of an optimal received signal-to-noise ratio (SNR) for the deployed nodes and show that improper selection of the distribution for modeling of the variations in the channel can lead to an overuse of energy by a factor of four or even higher.
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- Ahlund, Mikael, 1959-, et al.
(författare)
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Foreword
- 2015
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Ingår i: Art Bulletin of Nationalmuseum Stockholm. - Stockholm : Nationalmuseum. - 2001-9238. ; 21:2014, s. 9-10
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Tidskriftsartikel (populärvet., debatt m.m.)
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| 10. |
- Andersson, Linda, 1973, et al.
(författare)
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PLD1 and ERK2 regulate cytosolic lipid droplet formation
- 2006
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Ingår i: J Cell Sci. ; 119:Pt 11, s. 2246-57
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Tidskriftsartikel (refereegranskat)abstract
- We have previously uncovered roles for phospholipase D (PLD) and an unknown cytosolic protein in the formation of cytosolic lipid droplets using a cell-free system. In this report, PLD1 has been identified as the relevant isoform, and extracellular signal-regulated kinase 2 (ERK2) as the cytosolic protein. Increased expression of PLD1 increased lipid droplet formation whereas knockdown of PLD1 using siRNA was inhibitory. A role for ERK2 in basal lipid droplet formation was revealed by overexpression or microinjection, and ablation by siRNA knockdown or pharmacological inhibition. Similar manipulations of other Map kinases such as ERK1, JNK1 or JNK2 and p38alpha or p38beta were without effect. Insulin stimulated the formation of lipid droplets and this stimulation was inhibited by knockdown of PLD1 (by siRNA) and by inhibition or knockdown (by siRNA) of ERK2. Inhibition of ERK2 eliminated the effect of PLD1 on lipid droplet formation without affecting PLD1 activity, suggesting that PLD1 functions upstream of ERK2. ERK2 increased the phosphorylation of dynein which increased the amount of the protein on ADRP-containing lipid droplets. Microinjection of antibodies to dynein strongly inhibited the formation of lipid droplets, demonstrating that dynein has a central role in this formation. Thus dynein is a possible target for ERK2.
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