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Tissue engineering is an enabling technology that can be used to repair, replace, and regenerate different types of biological tissues and holds great potential in various biomedical applications. As the first line of defense for the human body, the skin has a complex structure. When skin is injured by trauma or disease, the skin tissues may regenerate under natural conditions, though often resulting in irreversible and aesthetically unpleasant scarring. The development of skin tissue engineering strategies was reviewed. Although the traditional approaches to skin tissue engineering have made good progress, they are still unable to effectively deal with large-area injuries or produce full-thickness grafts. In vitro three-dimensional (3D) skin constructs are good skin equivalent substitutes and they have promoted many major innovative discoveries in biology and medicine. 3D skin manufacturing technology can be divided into two categories: scaffold-free and scaffold-based. The representatives of traditional scaffold-free approaches are transwell/Boyden chamber approach and organotypic 3D skin culture. Because of its low cost and high repeatability, the scaffold-free 3D skin model is currently commonly used for cytotoxicity analysis, cell biochemical analysis, and high-throughput cell function. At present, many drug experiments use artificial skin developed by traditional approaches to replace animal models. 3D bioprinting technology is a scaffold-based approach. As a novel tissue manufacturing technology, it can quickly design and build a multi-functional human skin model. This technology offers new opportunities to build tissues and organs layer by layer, and it is now used in regenerative medicine to meet the increasing need for tissues and organs suitable for transplantation. 3D bioprinting can generate skin substitutes with improved quality and high complexity for wound healing and in vitro disease modeling. In this review, we analyze different types of conventional techniques to engineer skin and compare them with 3D bioprinting. We also summarized different types of equipment, bioinks, and scaffolds used in 3D skin engineering. In these skin culture techniques, we focus on 3D skin bioprinting technology. While 3D bioprinting technology is still maturing and improvements to the techniques and protocols are required, this technology holds great promise in skin-related applications.

The hydrophilicity and inherent flammability of cotton textiles severely limit their usage. To solve these drawbacks, a superhydrophobic and flame-retardant (SFR) coating made of chitosan (CH), ammonium polyphosphate (APP), and TiO2-SiO2-HMDS composite was applied to cotton fabric using simple layer-by-layer assembly and dip-coating procedures. First, the fabric was alternately immersed in CH and APP water dispersions, and then immersed in TiO2-SiO2-HMDS composite to form a CH/APP@TiO2-SiO2-HMDS coating on the cotton fabric surface. SEM, EDS, and FTIR were used to analyze the surface morphology, element composition, and functional groups of the cotton fabric, respectively. Vertical burning tests, microscale combustion calorimeter tests, and thermogravimetric analyses were used to evaluate the flammability, combustion behavior, thermal degradation characteristics, and flame-retardant mechanism of this system. When compared to the pristine cotton sample, the deposition of CH and APP enhanced the flame retardancy, residual char, heat release rate, and total heat release of the cotton textiles. The superhydrophobic test results showed that the maximal contact angle of SFR cotton fabric was 153.7°, and possessed excellent superhydrophobicity. Meanwhile, the superhydrophobicity is not lost after 10 laundering cycles or 50 friction cycles. In addition, the UPF value of CH/APP@TiO2-SiO2-HMDS cotton was 825.81, demonstrating excellent UV-shielding properties. Such a durable SFR fabric with a facile fabrication process exhibits potential applications for both oil/water separation and flame retardancy.

Yarn-based strain sensor is an emerging candidate for the fabrication of wearable electronic devices. The intrinsic properties of yarn, such as excellent lightweight, flexibility, stitchability, and especially its highly stretchable performance, stand out the yarn-based strain sensor from conventional rigid sensors in detection of human body motions. Recent advances in conductive materials and fabrication methods of yarn-based strain sensors are well reviewed and discussed in this work. Coating techniques including dip-coating, layer by layer assemble, and chemical deposition for deposition of conductive layer on elastic filament were first introduced, and fabrication technology to incorporate conductive components into elastic matrix via melt extrusion or wet spinning was reviewed afterwards. Especially, the recent advances of core–sheath/wrapping yarn strain sensor as-fabricated by traditional spinning technique were well summarized. Finally, promising perspectives and challenges together with key points in the development of yarn strain sensors were presented for future endeavor.

Yarn-shaped supercapacitors are favored due to their small size, high specific capacitance, and light weight. Herein, we reported a distinctive type of ply twist yarn supercapacitor by in situ polymerization of pyrrole on carbon nanotubes (CNTs)/cotton ring spun yarns. CNTs and polypyrrole (PPy) were successfully embedded into the cotton yarns with a ply twist structure. The as-developed electrode exhibited excellent electrical conductivity (20 Ω/cm), good mechanical properties (59.8 MPa, 24.6%), a high specific capacitance of 386.5 mF/cm2 with the current density of 1 mA/cm2, and ideal cycle stability with the retention of 87.8% after 5000 cycles. Meanwhile, the assembled supercapacitor showed a power density of 278.4 μW/cm2 and an energy density of 13.21 μWh/cm2. It also presented outstanding capacitive performance under different angles. This facile ply twist method provided new possibilities for one-dimensional (1D) supercapacitor and flexible wearable electronics applications.

The applications of a variety of bioactive ceramics such as hydroxyapatite (HA) in orthopedics are limited by their insufficient mechanical properties, especially poor fracture toughness. Thus, further extending the clinical applications of these materials warrants the enhancement of their mechanical properties. Although the reinforcement of ceramics by 2D nanomaterials has been well recognized, integrated structural, mechanical, and functional considerations have been neglected in the design and synthesis of such composite materials. Herein, we report the first use of silica-coated reduced graphene oxide (S-rGO) hybrid nanosheets to create bioceramic-based composites with simultaneously enhanced mechanical and biological properties. In the representative HA-based bioceramic systems prepared by spark plasma sintering, S-rGO incorporation was found to be more effective for increasing the Young's modulus, hardness, and fracture toughness than the incorporation of uncoated reduced GO (rGO). Furthermore, when assessed with osteoblast-like MG-63 cells, such novel materials led to faster cell proliferation and higher cell viability and alkaline phosphatase activity than are generally observed with pure HA; additionally, cells demonstrate stronger affinity to S-rGO/HA than to rGO/HA composites. The S-rGO/bioceramic composites are therefore promising for applications in orthopedic tissue engineering, and this research provides valuable insights into the fabrication of silica-coated hybrid nanosheet-reinforced ceramics. Nanyang Technological University This study was supported by Nanyang Technological University (NTU,Grant No. M4080160).

The cotton textiles with superhydrophobic and flame-retardant properties used in this study were manufactured by combining nano APP@SiO2 with silicone oil. To generate nano APP@SiO2 particles, the APP is coated with nano SiO2. The nano APP@SiO2 improves the flame retardancy of cotton textiles while altering the surface roughness of cotton fabrics, making them superhydrophobic after being treated with silicone oil. Cotton fabrics’ surface topography, chemical components, crystalline structure, thermal stability, flame-retardant, and superhydrophobic properties were investigated. The modified cotton fabric demonstrated not only exceptional superhydrophobicity with a WCA of 151.28°, but also good flame-retardant property. This multifunctional cotton fabric offers a wide range of commercial applications.

The flexible strain sensor can transform the micro or macro deformation into the visual electrical signals for monitoring the physiological and motor characteristics of human body. However, the current commercial strain sensors generally have some shortcomings such as large stiffness and small strain range. In this work, a flexible compressive strain sensor with the 3D conductive network was fabricated by using biomacromolecule sericin protein dispersed carbon nanotubes (SSCNTs) as the conductive material and melamine foam (MF) as the elastic matrix. The results showed that the sensitivity of MF/SSCNTs elastic foam was 1.36 in the strain range of 0-70% with the CNTs content of 10 wt% and the cyclic compressive sensing performance was stable for at least 1600 cycles. This kind of flexible compressive strain sensor is environmentally friendly, low cost, simple process, and provides a new method for the preparation of green flexible sensor.

Steel ring reinforcement technology is an effective method to eliminate the damage of tunnel structure caused by ground load, surrounding foundation pit and underground water source. The grouting material used to fill the gap between the tunnel segment and the steel ring should have the characteristics of low viscosity, high strength, rapid curing at room temperature and anti-subway vibration. In this work, a special polyurethane modified epoxy resin grouting was fabricated to overcome the inherent brittleness of epoxy resin, and was combined with the reactive diluent and the amine curing agent to suit the above applications. The results showed that both tensile and impact strength of epoxy resin grouting modified by polyurethane were improved obviously compared with those without modification, presenting an obvious toughening effect. Although the viscosity increased slightly, it can still meet the perfusion requirements of steel ring reinforcement of subway tunnels.

In this work, the superhydrophobic and UV-resistant cotton fabrics were fabricated via combining the nano titanium dioxide (TiO2) and silicone oil. The nano-TiO2 makes cotton fabrics possess outstanding ultraviolet (UV) resistance property, while increases the micro and nano size rough structure on the surface of cotton fabric. Then the cotton fabric was hydrophobically treated with silicone oil to make it superhydrophobic. The chemical constituents, structures, superhydrophobic and UV-resistant performance of cotton fabrics were analyzed. The cotton fabric treated with titanium dioxide and silicone oil not only showed excellent superhydrophobicity, but also displayed good UV-resistant ability. Water contact angle and UPF value can reach 161.32° and 55.17 respectively. Such multifunctional cotton fabric has broad commercial application prospects.

Epoxy structural adhesive has good mechanical properties, especially high adhesion, low shrinkage rate, and high stability, widely used in steel plate reinforcement, crack repair, bridge splicing, and concrete bonding, etc. However, due to the high cross-linking density and high internal stress after curing, its shortcomings, such as brittleness, the poor performance of fatigue resistance and heat resistance, limit its application in special track engineering. In this work, two kinds of epoxy structural adhesives (EPA-1, EPA-2) with low viscosity and room temperature curing were synthesized by selecting different bisphenol A epoxy resin and active diluent as component A and modified amine curing agent as component B. The results showed that EPA-1 and EPA-2 presented significant toughness compared with the classic construction adhesive (AralditeXH160). The yield strengths of EPA-1 and EPA-2 were 4.88 MPa and 13.13 MPa, and the shear strengths were 11.93 MPa and 13.08 MPa, respectively, showing good adhesive properties. In addition, the viscosities of EPA-1 and EPA-2 were 127 mPa·s and 308 mPa·s, respectively, and their decomposition temperatures were all above ∼280 °C, which indicated that the self-made epoxy structural adhesives could be used for the repair of cracks in the vibration subway tunnel.

Carbon nanotube (CNT) possesses eminent mechanical properties and has been widely utilized to toughen bioceramics. Major challenges associated with CNT-reinforced bioceramics include the inhomogeneous dispersion of CNTs and the insufficient interfacial strength between the two phases. To address such issues, this research describes the first use of silica-coated CNT (S-CNT) core-shell structures to reinforce bioceramics using hydroxyapatite (HA) as a representative matrix. HA-based composites with 0.1–2 wt% S-CNT are sintered by spark plasma sintering to investigate their mechanical and biological properties. It is found that when 1 wt% raw CNT (R-CNT) is added, very limited increases in fracture toughness ( K IC ) is observed. By contrast, the incorporation of 1 wt% S-CNT increased the K IC of HA by 101.7%. This is attributed to more homogeneously dispersed fillers and stronger interfacial strengths. MG63 cells cultured on the 1 wt% S-CNT/HA pellets are found to proliferate faster and possess significantly higher alkaline phosphatase activities than those grown on the HA compacts reinforced with 1 wt% R-CNT, probably by virtue of the released Si ions from the SiO2 shell. Therefore, the S-CNT core-shell structures can improve both mechanical and biological properties of HA more effectively than the conventionally used R-CNTs. The current study also presents a novel and effective approach to the enhancement of many other biomedical and structural materials through S-CNT incorporation.

3D graphene foam was recently demonstrated to exhibit excellent electromagnetic interference (EMI) shielding performance. In this work, we prepared 3D graphene foams by incorporating a surface modification process of graphene via self-polymerization of dopamine with a subsequent foaming process. The multiple roles played by polydopamine (PDA), including as nitrogen doping source and as an enhancement tool to achieve higher extent of reduction of the graphene through providing wider pathways and larger accessible surface areas were discussed in detail. Despite the presence of the PDA which acted as barriers among the graphene layers that hindered the electrons movement, the enhanced reduction of graphene sheets and the polarization effects introduced by PDA decoration compensated the negative effect of the barrier on EMI shielding effectiveness (SE). As a result, the PDA decorated 3D graphene foams showed improved EMI shielding effectiveness (SE) compared to PDA-free graphene foam (from 23.1 to 26.5dB). More significantly, the EMI shielding performance of the PDA decorated graphene foam was much superior to all existing carbon-based porous materials when the thickness of the specimen was considered.

Electromagnetic interference (EMI) shielding performance of chemically and thermally reduced graphene aerogels (GAs) was systematically studied. The EMI shielding mechanisms were extensively analyzed in terms of the distinct surface characteristics resulted from the different reduction methods for the first time. EMI shielding effectiveness (SE) of chemically and thermally reduced GAs reached 27.6 (GAC) and 40.2 dB (GAT) at the thickness of 2.5 mm, respectively. It was found that the introduction of nitrogen atoms through chemical reduction induced localized charges on the carbon backbone leading to strong polarization effects of GAC. The relatively incomplete reduction caused a large number of side polar groups which prevented the graphene sheets from π-π stacking. In contrast, the higher extent of reduction of graphene sheets in GAT left a smaller amount of side polar groups and formed more sp2 graphitic lattice, both factors favored π-π stacking between the adjacent graphene sheets, resulting in higher electrical conductivity and enhanced EMI SE. The EMI shielding performance of the GAs prepared outperformed the recent reported porous carbon materials with respect to the absolute SE value at the similar thickness and/or density.

Strain sensing is one of the core parts of smart fabric which can be expressed by electrical signals affected by external forces. In this paper, the strain sensing functional fabric was prepared by using the acidified carbon nanotubes (a-CNTs) as the conductive layer and the waterborne polyurethane (WPU) as the adhesive based on foam finishing method. The results showed that many hydroxyl and carboxyl groups were introduced into the surface of CNTs through acidification, which improved their dispersibility in aqueous solution. The blended film of a-CNTs and anionic WPU had excellent conductive properties. When the ratio of a-CNT to WPU was 9:1, the fabric had the smallest resistivity, about 0.13 Ω⋅m, and the corresponding tensile sensing sensitivity up to 55.2.

Soft micro-environment is one of the most important requirements for fast responses of liquid crystals (LCs) to external stimuli; however, the drawback of poor mechanical properties for LCs limits their further applications. In this work, the storage modulus ( G ′) of the LC physical gels, nematic 4-pentyl-4′-cyanobiphenyl (5CB) and 1,3:2,4-di- O -benzylidene- D-sorbitol (DBS), has been greatly enhanced by the addition of nano-silica into physical gels. The composite gels are formed through the synergistic effects of the nanoparticle and the gelator. The phase transition behaviors, morphologies, dynamic rheological behaviors and electro-optical properties of the composite gels were investigated using differential scanning calorimeter, polarized optical microscope and field emission scanning electron microscope, rheometer and LCD parameter tester, respectively. Compared with the LC physical gel without nano-silica, with the increase of nano-silica content from 0.1wt% to 4.0wt% at a fixed DBS content of 2.0wt%, the network texture of composite gels was changed from nano-fibrillar to spherulite-like. The G ′ increased firstly and then decreased with a maximum value of 1.5×105 Pa at the nano-silica content of 2.0wt%. The threshold voltage ( V th) and the off time ( τ off) increased within 1 time and 2 times, respectively. When the amount of nano-silica was only 0.5wt%, the G ′ of the composite gel was improved to 105 Pa, an order of magnitude higher than the gel without nanoparticles. Meanwhile, its V th and τ off only increased 46% and 63%, respectively. This work opens a new window to the applications of LCs with excellent self-supporting ability and fast switch responses.

The smart fabric is a new material that began to develop in the 1990s, and on the basis of the nature and function of original material, it joined the features of intelligent perception. On the performance, intelligent fiber can sense the changes of heat, light, chemistry, mechanical, temperature, and electromagnetic, then react accordingly. For smart textiles, the sensor is the core part, now most commonly used micro/nano strain sensor are using silicon and zinc oxide and others inorganic as main material. But inorganic materials have limited deformation ability, once deformation occurs, the sensor will be strictly damaged. So, the development of flexible, high sensitivity, wide range of strain of the flexible intelligent fiber strain sensor has a very important application prospect. For the stretch-able sensor, the prepared conductive material must be placed on the substrate of the flexible polymer. In this paper, graphene is used as conductive material to construct an orderly conductive layer. Waterborne polyurethane was used as dispersant and adhesive, then strengthen the interface between the layer of conductive material and elastic fabric binding force, and finally prepare a kind of high sensitivity, wide strain range, stable performance and high elastic intelligent fibers.

Versatile and reversibly rapid responsive one-dimensional photonic crystals with a diffraction efficiency of 97%, which consisted of uniformly 273 ± 48 nm wide liquid crystal belts within transmission holographic polymer dispersed liquid crystal (HPDLC) gratings, were formulated by a facile single step holography based on a hyperbranched monomer. The effect of the monomer average functionality on the photopolymerization kinetics and the electro-optical performances as well as the grating morphologies was investigated. The results show that the low intrinsic viscosity of the hyperbranched monomer accounts for a well-structured morphology in terms of providing a prolonged gelation time for the liquid crystals to diffuse from the light illumination region during the holographic polymerization induced phase separation. Another intriguing observation is that with an increase in the hyperbranched monomer loading, the diffraction efficiency of the HPDLC gratings gradually increases from zero to an average of 94% and then levels off. This is quite different from previous results that gave less than a 50% diffraction efficiency when the monomer average functionality was larger than 4.

Interaction of cell surface glycoproteins with endogenous lectins on the cell surface regulates formation and maintenance of plasma membrane domains, clusters signaling complexes, and controls the residency time of glycoproteins on the plasma membrane. Galectin-9 is a soluble, secreted lectin that binds to glycoprotein receptors to form galectin–glycoprotein lattices on the cell surface. Whereas galectin-9 binding to specific glycoprotein receptors induces death of CD4 Th1 cells, CD4 Th2 cells are resistant to galectin-9 death due to alternative glycosylation. On Th2 cells, galectin-9 binds cell surface protein disulfide isomerase (PDI), increasing retention of PDI on the cell surface and altering the redox status at the plasma membrane. Cell surface PDI regulates integrin function on platelets and also enhances susceptibility of T cells to infection with HIV. We find that galectin-9 binding to PDI on Th2 cells results in increased cell migration through extracellular matrix via β3 integrins, identifying a unique mechanism to regulate T-cell migration. In addition, galectin-9 binding to PDI on T cells potentiates infection with HIV. We identify a mechanism for regulating cell surface redox status via a galectin–glycoprotein lattice, to regulate distinct T-cell functions.

β-Galactoside-binding lectin 9 (galectin-9) is a tandem repeat-type member of the galectin family. It was initially characterized as an eosinophil chemoattractant and an inducer of apoptosis in thymocytes. Subsequently, galectin-9 was identified as a ligand for transmembrane immunoglobulin mucin domain 3 (Tim-3), a type I glycoprotein induced on T cells during chronic inflammation. Work in autoimmune diseases and chronic viral infections have led to the current hypothesis that the function of Tim-3 is to limit immune responses. However, it is still not known to what degree these effects are due to the galectin-9/Tim-3 interaction. In this study, we show that galectin-9 is not limited to the role of a pro-apoptotic agent, but that it can also induce the production of pro-inflammatory cytokines from T helper cells. This effect is dose-dependent and does not require Tim-3. These findings suggest that the effects of galectin-9 on T cells are more complex than previously thought and are mediated by additional receptors apart from Tim-3.

Galectin-1, a beta-galactoside-binding protein highly expressed in the thymus, induces apoptosis of specific thymocyte subsets and activated T cells. Galectin-1 binds to N- and O-glycans on several glycoprotein receptors, including CD7, CD43, and CD45. Here we show that galectin-1 signaling through CD45, which carries both N- and O-glycans, is regulated by CD45 isoform expression, core 2 O-glycan formation and the balance of N-glycan sialylation. Regulation of galectin-1 T cell death by O-glycans is mediated through CD45 phosphatase activity. While galectin-1 signaling in cells expressing low molecular weight isoforms of CD45 requires expression of core 2 O-glycans (high affinity ligands for galectin-1), galectin-1 signaling in cells expressing a high molecular weight isoform of CD45 does not require core 2 O-glycans, suggesting that a larger amount of core 1 O-glycans (low affinity ligands for galectin-1) is sufficient to overcome lack of core 2 O-glycans. Furthermore, regulation of galectin-1 signaling by alpha2,6-sialylation of N-glycans is not solely dependent on CD45 phosphatase activity and can be modulated by the relative expression of enzymes that attach sialic acid in an alpha2,6- or alpha2,3-linkage. Thus, N- and O-glycans modulate galectin-1 T cell death by distinct mechanisms, and different glycosylation events can render thymocytes susceptible or resistant to galectin-1.

Detection of exposure to biological threat agents has relied on ever more sensitive methods for pathogen identification, but that usually requires pathogen proliferation to dangerous, near untreatable levels. Recent events have demonstrated that assessing exposure to a biological threat agent well in advance of onset of illness or at various stages post-exposure is invaluable among the diagnostic options. There is an urgent need for better diagnostic tools that will be sensitive, rapid, and unambiguous. Since human clinical cases of illness induced by biothreat agents are, fortunately, rare, use of animal models that closely mimic the human illness is the only in vivo option. Such studies can be very difficult and expensive; therefore, maximizing the information obtained from in vitro exposures to peripheral blood mononuclear cells (PBMCs) provide an opportunity to investigate dose/time variability in host responses. In our quest to study staphylococcal enterotoxin B (SEB) induced host gene expression patterns, we addressed two core issues using microarray analysis and predictive modeling. Our first objective was to determine gene expression patterns in human PBMCs exposed to SEB in vitro. Second, we compared the in vitro data with host responses gene expression patterns in vivo using PBMCs from an animal model of SEB intoxication that closely replicates the progression of illness in humans. We used cDNA microarrays to study global gene expression patterns in piglets intoxicated with SEB. We applied a supervised learning method for class prediction based on the k-nearest neighbor algorithm for the data obtained in piglets exposed to SEB in vivo against a training data set. This data set included gene expression profiles derived from in vitro exposures to eight different pathogens (Bacillus anthracis, Yersinia pestis, Brucella melitensis, SEB, cholera toxin, Clostridium botulinum toxin A, Venezuelan equine encephalitis, and Dengue-2) in PBMCs. We found that despite differences in gene expression profiles between in vitro and in vivo systems, there exists a subset of genes that show correlations between in vitro and in vivo exposures, which can be used as a predictor of exposure to SEB in vivo.

Galectins regulate cellular functions by binding to glycan ligands on cell surface glycoprotein receptors. Prototype galectins, such as galectin-1, are one carbohydrate recognition domain (CRD) monomers that noncovalently dimerize, whereas tandem-repeat galectins, such as galectin-9, have two non-identical CRDs connected by a linker domain. Dimerization of prototype galectins, or both CRDs in tandem-repeat galectins, is typically required for the crosslinking of glycoprotein receptors and subsequent cellular signaling. Several studies have found that tandem-repeat galectins are more potent than prototype galectins in triggering many cell responses, including cell death. These differences could be due to CRD specificity, the presence or absence of a linker domain between CRDs, or both. To interrogate the basis for the increased potency of tandem-repeat galectins compared with prototype galectins in triggering cell death, we created three tandem-repeat galectin constructs with different linker regions joining identical galectin-1 CRDs, so that any differences we observed would be due to the contribution of the linker region rather than due to CRD specificity. We found that random-coil or rigid α-helical linkers that permit separation of the two galectin-1 CRDs facilitated the formation of higher-order galectin multimers and that these galectins were more potent in binding to glycan ligands and cell surface glycoprotein receptors, as well as triggering T cell death, compared with native galectin-1 or a construct with a short rigid linker. Thus, the increased potency of tandem-repeat galectins compared with prototype galectins is likely due to the ability of the linker domain to permit intermolecular CRD interactions, resulting in the formation of higher-order multimers with increased valency, rather than differences in CRD specificity.

The galectin family of lectins regulates multiple biologic functions, such as development, inflammation, immunity, and cancer. One common function of several galectins is the ability to trigger T cell death. However, differences among the death pathways triggered by various galectins with regard to glycoprotein receptors, intracellular death pathways, and target cell specificity are not well understood. Specifically, galectin-9 and galectin-1 both kill thymocytes, peripheral T cells, and T cell lines; however, we have found that galectin-9 and galectin-1 require different glycan ligands and glycoprotein receptors to trigger T cell death. The two galectins also utilize different intracellular death pathways, as galectin-9, but not galectin-1, T cell death was blocked by intracellular Bcl-2, whereas galectin-1, but not galectin-9, T cell death was blocked by intracellular galectin-3. Target cell susceptibility also differed between the two galectins, as galectin-9 and galectin-1 killed different subsets of murine thymocytes. To define structural features responsible for distinct activities of the tandem repeat galectin-9 and dimeric galectin-1, we created a series of bivalent constructs with galectin-9 and galectin-1 carbohydrate recognition domains connected by different peptide linkers. We found that the N-terminal carbohydrate recognition domain and linker peptide contributed to the potency of these constructs. However, we found that the C-terminal carbohydrate recognition domain was the primary determinant of receptor recognition, death pathway signaling, and target cell susceptibility. Thus, carbohydrate recognition domain specificity, presentation, and valency make distinct contributions to the specific effects of different galectins in initiating T cell death.

We have used piglets as an animal model for studying the toxic effects of staphylococcal enterotoxins (SEs). Piglets are easy to handle, easy to carry out vital measurements, inexpensive, and more importantly, express remarkably similar pathological symptoms and responses to SE intoxication as humans at comparable doses. Microarray analyses are used to study the effect of many infections on gene expression profile in peripheral blood mononuclear cells. This high throughput application offers detailed depiction of alteration at the molecular levels. When using high throughput gene expression analysis, there is a high possibility of finding genes that vary normally in the tissues under study. It is necessary to verify genes that are normally differentially expressed between piglets. To evaluate the normal physiological variation in gene expression in vivo in piglets, we used cDNA microarray to measure gene expression levels in peripheral blood mononuclear cells from 10 normal Yorkshire piglets. We used analysis of variance to determine genes that showed statistically significant variations across piglets. Out of 1185 genes, 19 (1.6%) genes revealed statistically significant variance between RNA samples. Some of these varying genes are involved in stress response, immune response, and transcription. This study facilitates the characterization of gene expression base line needed for meaningful interpretation of microarray data.