Transforming growth factor (TGF)-β inhibits T cell proliferation and differentiation. TGF-β has been shown to inhibit the expression of transcription factors such as GATA-3 and T-bet that play important roles in T cell differentiation. Here we show that TGF-β inhibits T cell differentiation at a more proximal step. An early event during T cell activation is increased intracellular calcium levels. Calcium influx in activated T cells and the subsequent activation of transcription factors such as NFATc, events essential for T cell differentiation, are modulated by the Tec kinases that are downstream of the T cell receptor and CD28. We show that in stimulated CD4+ T cells, TGF-β inhibits phosphorylation and activation of the Tec kinase Itk, increase in intracellular Ca2+ levels, NFATc translocation, and activation of the mitogen-activated protein kinase ERK that together regulate T cell differentiation. Our studies suggest that by inhibiting Itk, and consequently Ca2+ influx, TGF-β limits T cell differentiation along both the Th1 and Th2 lineages.

Planar patch-clamp has revolutionized ion-channel measurement by eliminating laborious manipulation from the traditional micropipette approach and enabling high throughput. However, low yield in gigaseal formation and/or relatively high cost due to microfabricated processes are two main drawbacks. This paper presents patch clamping on glass substrate-an economical solution without sacrificing gigaseal yield rate. Two-stage CO(2) laser drilling methodology was used to generate an hourglass, funnel-like aperture of a specified diameter with smooth and debris-free surfaces on 150 microm borosilicate cover glass. For 1-3 microm apertures as patch-clamp chips, seal resistance was tested on human embryonic kidney, Chinese hamster ovary, and Jurkat T lymphoma cells with a gigaseal success rate of 62.5%, 43.6% and 66.7% respectively. Results also demonstrated both whole-cell and single channel recording on endogenously expressed ion channels to confirm the capability of different patch configurations.

Few studies have compared how rehabilitative post-acute care affects recovery of walking ability and other functions after stroke in different age groups. After propensity score matching (1:1), 316 stroke patients were separated into an aged group (age ≥65 years, n=158) and a non-aged group (age <65 years, n=158). Both groups significantly improved in Barthel index, EuroQol-5 dimension, Berg balance scale, 6-minute walking distance and 5-meter walking speed ( P <0.001). The non-aged group had significantly larger improvements in Berg balance scale, instrumental activities of daily living, EuroQol-5 dimension and 6-minute walking distance ( P <0.001) compared to the aged group. The two groups did not significantly differ in Barthel index, 5-meter walking speed, length of stay, and cost. The aged group had poorer walking ability and poorer instrumental activities of daily living compared to the non-aged group. After intensive rehabilitative post-acute care, however, the aged group improved in walking ability, functional performance and mental health. Intensive strength training for unaffected lower limbs in the stroke patients achieved good recovery of walking ability and other functions. Overall, intensive rehabilitative post-acute care improved self-care ability and decreased informal care costs. Rehabilitative PAC under per-diem reimbursement is efficient and economical for stroke patients in an aging society.

This paper presents a magnetically driven valve via a permanent magnet pressing a spacer against deformable polydimethylsiloxane (PDMS) to fully close a microchannel. Its ability for electrical isolation, time response, and resistance to backpressure are interrogated. Simulation of the valve closing process was commenced along with experimental verification. Effects of PDMS thickness, and dimension and aspect ratio of microchannels were characterized. Up to 10 GΩ electrical isolation was demonstrated, as well as 50-70 ms valve response and ∼200 kPa resistible pressure. On-demand actuation for arbitrary flow patterns further quantifies its utility. With advantages of simple fabrication, flexible valving location, and no external power requirement, the on/off valve could be leveraged for proof-of-concept microfluidic devices and other applications.

Reaction of aminophosphinimine [RHN(CH(2))(2)N[double bond, length as m-dash]PPh(3)] (R = H, Et) with Re(2)(CO)(10) provided the NH-functionalized carbene rhenium complex [Re(2)(CNHCH(2)CH(2)NR)(CO)(9)] (3a, R = H, 3b, R = Et). Treatment of 3 with Br(2) provided the mono nuclear [Re(CNHCH(2)CH(2)NR)(CO)(4)Br] (1, R = H, 2, R = Et). However, NH-functionalized carbene complexes 1-3 did not undergo N-alkylation with alkyl halides to yield the N-substituted NHC complexes. The direct ligand substitution of [Re(CO)(5)Br] with a carbene donor was employed to prepare [Re(IMes(2))(CO)(4)Br] (6a, IMes(2) = 1,3-di-mesitylimidazol-2-ylidene; 6b, IMes(2) = 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene). Analyses of spectroscopic and crystal data of 6a and 6b show similar corresponding data among these complexes, suggesting the saturated and unsaturated NHCs have similar bonding with Re(I) metal centers. Reduction of 6a and 6b with LiEt(3)BH yielded the corresponding hydrido complexes 7a-b [ReH(CO)(4)(IMes(2))], but not 1 and 2. Ligand substitution of 1, 6a and 6b toward 2,2'-bipyridine (bipy) was investigated. Crystal structures of 1, 3a-b, 6a-b and 7b were determined for characterization and comparison.

The photoluminescence (PL) and reflectivity characteristics of zinc oxide nanopillars (ZnO-NPs) grown on indium-tin-oxide (ITO)-coated glasses were investigated. The room temperature PL showed bright white-light emission for the undoped ZnO-NPs grown at 600 °C, suggesting the close relation between the optical characteristic and the growth conditions being carried out for obtaining the present ZnO-NPs. The reflectivity of the as-grown ZnO-NPs array was about ∼29% with the wavelength of the incident light ranging from 200 to 1800 nm. Nevertheless, the reflectance reduced significantly to less than 9.9% when a layer of gold (Au) was deposited on ZnO-NPs by sputtering for 5 min, corresponding to more than 65% reduction in Au-coated ZnO-NPs (Au/ZnO-NPs). Moreover, the angle-resolved reflectance measurements on the present Au/ZnO-NPs array show an omnidirectional light-trapping characteristic. These remarkable characteristics, broadband and omnidirectional light-trapping of Au/ZnO-NPs, are attributed to the extended effective optical path of the incident light due to subwavelength scattering resulting from the presence of Au nanoparticles.

No abstract

A Newly Discovered Function for C1 Inhibitor, Removal of the Entire C1qr 2 s 2 Complex from Immobilized Human IgG Subclasses," by Chang-Hung Chen and Robert J. Boackle, pages 68 -74: On page 72, Figs. 5b and 6 contain errors. In Fig. 5b, the levels of Human IgG should be 0.5, 1.0, and 2.0 g/well, rather than 5, 10, and 20 g/well, respectively. In Fig. 6, the level of immobilized IgG per well should be 0.5 g, rather than 5.0 g. The legends were correct as printed. For the reader's convenience, the corrected figures and their legends are printed here.This erratum is Article ID clim.1998.4670. FIG. 5. Addition of purified C1 INH to bound activated C1. Purified activated human C1 was incubated with immobilized IgG preparations for 30 min at 37°C before the addition of increased doses of purified C1 INH. Subsequently, anti-C1q-HRP was used to probe for C1q binding. (a) The addition of C1 INH significantly reduced C1q (C1) binding in wells with immobilized human IgG. In controls with purified C1q, addition of C1 INH did not affect bound C1q. This result suggested that the entire C1 complex is needed for C1 INH to dislodge C1q from immobilized IgG preparations. (b) Similar experiments were performed to study the effects of C1 INH on the displacement of C1 (C1q) from different doses of immobilized IgG. More C1q binding was detected on higher concentrations of immobilized IgG even in the presence of C1 INH. Data represent triplicate determinations of a single experiment and presented as means Ϯ SE (data from one of three experiments, similarly performed). FIG. 6. Prevention of the dislodging of C1q (within C1 complex) by presaturating C1 INH with excess activated C1s. Various doses of activated C1s were used to neutralize the function of C1 INH and these C1s-C1 INH mixtures were then applied to C1-bound immobilized human IgG. After incubation, bound C1q was probed with anti-C1q-HRP. Data represent triplicate determinations of a single experiment and are presented as means Ϯ SE (data from one of three experiments, similarly performed).