37 research outputs found
Double-Layer Systems at Zero Magnetic Field
We investigate theoretically the effects of intralayer and interlayer
exchange in biased double-layer electron and hole systems, in the absence of a
magnetic field. We use a variational Hartree-Fock-like approximation to analyze
the effects of layer separation, layer density, tunneling, and applied gate
voltages on the layer densities and on interlayer phase coherence. In agreement
with earlier work, we find that for very small layer separations and low layer
densities, an interlayer-correlated ground state possessing spontaneous
interlayer coherence (SILC) is obtained, even in the absence of interlayer
tunneling. In contrast to earlier work, we find that as a function of total
density, there exist four, rather than three, distinct noncrystalline phases
for balanced double-layer systems without interlayer tunneling. The newly
identified phase exists for a narrow range of densities and has three
components and slightly unequal layer densities, with one layer being spin
polarized, and the other unpolarized. An additional two-component phase is also
possible in the presence of sufficiently strong bias or tunneling. The
lowest-density SILC phase is the fully spin- and pseudospin-polarized
``one-component'' phase discussed by Zheng {\it et al.} [Phys. Rev. B {\bf 55},
4506 (1997)]. We argue that this phase will produce a finite interlayer Coulomb
drag at zero temperature due to the SILC. We calculate the particle densities
in each layer as a function of the gate voltage and total particle density, and
find that interlayer exchange can reduce or prevent abrupt transfers of charge
between the two layers. We also calculate the effect of interlayer exchange on
the interlayer capacitance.Comment: 35 pages, 19 figures included. To appear in PR
Intramuscular injection of nerve growth factor as a model of temporomandibular disorder: nature, time-course, and sex differences characterising the pain experience
Background: Temporomandibular disorder (TMD) is a common condition that frequently transitions to chronic symptoms. Experimental pain models that mimic the symptoms of clinical TMD may be useful in understanding the mechanisms, and sex differences, present in this disorder. Here we aimed to comprehensively characterise the nature and time-course of pain, functional impairment and hyperalgesia induced by repeated intramuscular injection of nerve growth factor (NGF) into the masseter muscle, and to investigate sex differences in the NGF-induced pain experience. Methods: 94 healthy individuals participated in a longitudinal study with 30-day follow-up. NGF was injected into the right masseter muscle on Day 0 and Day 2. Participants attended laboratory sessions to assess pain (Numerical Rating Scale; NRS), functional limitation (mouth opening distance, Jaw Functional Limitation Scale; JFLS) and mechanical sensitization (pressure pain thresholds; PPTs) on Days 0, 2 and 5 and completed twice daily electronic pain dairies from Day 0 to day 30. Results: Peak pain averaged 2.0/10 (95 % CI: 1.6–2.4) at rest and 4.3/10 (95 % CI: 3.9–4.8) on chewing. Pain-free mouth opening distance reduced from 5.0 cm (95 % CI: 4.8–5.1 cm) on Day 0 to 3.7 cm (95 % CI: 3.5–3.9 cm) on Day 5. The greatest reduction in PPTs was observed over the masseter muscle. Females experienced higher pain, greater functional impairment, and greater sensitivity to mechanical stimuli than males. Conclusion: Intramuscular injection of NGF is a useful model with which to explore the mechanisms, and sex differences, present in clinical TMD
Fragmentation of tissue-resident macrophages during isolation confounds analysis of single-cell preparations from mouse hematopoietic tissues
Mouse hematopoietic tissues contain abundant tissue-resident macrophages that support immunity, hematopoiesis, and bone homeostasis. A systematic strategy to characterize macrophage subsets in mouse bone marrow (BM), spleen, and lymph node unexpectedly reveals that macrophage surface marker staining emanates from membrane-bound subcellular remnants associated with unrelated cells. Intact macrophages are not present within these cell preparations. The macrophage remnant binding profile reflects interactions between macrophages and other cell types in vivo. Depletion of CD169+ macrophages in vivo eliminates F4/80+ remnant attachment. Remnant-restricted macrophage-specific membrane markers, cytoplasmic fluorescent reporters, and mRNA are all detected in non-macrophage cells including isolated stem and progenitor cells. Analysis of RNA sequencing (RNA-seq) data, including publicly available datasets, indicates that macrophage fragmentation is a general phenomenon that confounds bulk and single-cell analysis of disaggregated hematopoietic tissues. Hematopoietic tissue macrophage fragmentation undermines the accuracy of macrophage ex vivo molecular profiling and creates opportunity for misattribution of macrophage-expressed genes to non-macrophage cells.Susan M. Millard, Ostyn Heng, Khatora S. Opperman, Anuj Sehgal, Katharine M. Irvine, Simranpreet Kaur, Cheyenne J. Sandrock, Andy C. Wu, Graham W. Magor, Lena Batoon, Andrew C. Perkins, Jacqueline E. Noll, Andrew C.W. Zannettino, David P. Sester, Jean-Pierre Levesque, David A. Hume, Liza J. Raggatt, Kim M. Summers, and Allison R. Petti