Hypoxia is a characteristic feature of the tissue microenvironment during bacterial infection. Here we report on our use of conditional gene targeting to examine the contribution of hypoxia-inducible factor 1, α subunit (HIF-1α) to myeloid cell innate immune function. HIF-1α was induced by bacterial infection, even under normoxia, and regulated the production of key immune effector molecules, including granule proteases, antimicrobial peptides, nitric oxide, and TNF-α. Mice lacking HIF-1α in their myeloid cell lineage showed decreased bactericidal activity and failed to restrict systemic spread of infection from an initial tissue focus. Conversely, activation of the HIF-1α pathway through deletion of von Hippel-Lindau tumor-suppressor protein or pharmacologic inducers supported myeloid cell production of defense factors and improved bactericidal capacity. HIF-1α control of myeloid cell activity in infected tissues could represent a novel therapeutic target for enhancing host defense.

Viscosity is a measure of the resistance of a fluid against gradients in flow (shear rate). Both flow and viscosity play an important role in all biological systems from the microscopic (e.g., cellular) to the systemic level. Many methods to measure viscosity and flow have drawbacks, such as the tedious and time-consuming measurement process, expensive instrumentation, or the restriction to bulk sample sizes. Fluorescent environment-sensitive dyes are known to show high sensitivity and high spatial and temporal resolution. Molecular rotors are a group of fluorescent molecules that form twisted intramolecular charge transfer (TICT) states upon photoexcitation and therefore exhibit two competing deexcitation pathways: fluorescence emission and non-radiative deexcitation from the TICT state. Since TICT formation is viscosity-dependent, the emission intensity of molecular rotors depends on the solvent's viscosity. Furthermore, shear-stress dependency of the emission intensity was recently described. Although the photophysical processes are widely explored, the practical application of molecular rotors as sensors for viscosity and the fluid flow introduce additional challenges. Intensity-based measurements are influenced by fluid optical properties and dye concentration, and solvent-dye interaction requires calibration of the measurement system to a specific solvent. Ratiometric dyes and measurement systems help solve these challenges. In addition, the combination of molecular rotors with specific recognition groups allows them to target specific sites, for example the cell membrane or cytoplasm. Molecular rotors are therefore emerging as new biosensors for both bulk and local microviscosity, and for flow and fluid shear stress on a microscopic scale and with real-time response.

The functioning of the immune system is finely balanced by the activities of pro-inflammatory and anti-inflammatory mediators or cytokines. Unregulated activities of these mediators can lead to the development of serious inflammatory diseases. In particular, enhanced tumour-necrosis factor-alpha (TNF-alpha) synthesis is associated with the development of rheumatoid arthritis, psoriatic arthritis and inflammatory bowel disease. Inhibiting TNF-alpha activities in these diseases has been remarkably successful. However, the current injectable protein therapies have associated risks and limitations. An oral, small molecule that regulates TNF-alpha biology could either replace the injectables or provide better disease control when used alone or in conjunction with existing therapies. In this review, we discuss briefly the present understanding of TNF-alpha-mediated biology and the current injectable therapies in clinical use, and focus on some of the new therapeutic approaches with oral, small-molecule inhibitors.

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Molecular rotors are a group of fluorescent molecules that form twisted intramolecular charge transfer (TICT) states upon photoexcitation. When intramolecular twisting occurs, the molecular rotor returns to the ground state either by emission of a red-shifted emission band or by nonradiative relaxation. The emission properties are strongly solvent-dependent, and the solvent viscosity is the primary determinant of the fluorescent quantum yield from the planar (non-twisted) conformation. This viscosity-sensitive behavior gives rise to applications in, for example, fluid mechanics, polymer chemistry, cell physiology, and the food sciences. However, the relationship between bulk viscosity and the molecular-scale interaction of a molecular rotor with its environment are not fully understood. This review presents the pertinent theories of the rotor-solvent interaction on the molecular level and how this interaction leads to the viscosity-sensitive behavior. Furthermore, current applications of molecular rotors as microviscosity sensors are reviewed, and engineering aspects are presented on how measurement accuracy and precision can be improved.

Synthetic matrices emulating the physicochemical properties of tissue-specific ECMs are being developed at a rapid pace to regulate stem cell fate. Biomaterials containing calcium phosphate (CaP) moieties have been shown to support osteogenic differentiation of stem and progenitor cells and bone tissue formation. By using a mineralized synthetic matrix mimicking a CaP-rich bone microenvironment, we examine a molecular mechanism through which CaP minerals induce osteogenesis of human mesenchymal stem cells with an emphasis on phosphate metabolism. Our studies show that extracellular phosphate uptake through solute carrier family 20 (phosphate transporter), member 1 (SLC20a1) supports osteogenic differentiation of human mesenchymal stem cells via adenosine, an ATP metabolite, which acts as an autocrine/paracrine signaling molecule through A2b adenosine receptor. Perturbation of SLC20a1 abrogates osteogenic differentiation by decreasing intramitochondrial phosphate and ATP synthesis. Collectively, this study offers the demonstration of a previously unknown mechanism for the beneficial role of CaP biomaterials in bone repair and the role of phosphate ions in bone physiology and regeneration. These findings also begin to shed light on the role of ATP metabolism in bone homeostasis, which may be exploited to treat bone metabolic diseases.bone metabolism | mineralized matrix | biomimetic material | phosphate signaling

Variations in fluid viscosity are linked to a variety of functions and diseases both at the cellular level (e.g., membrane and cytoplasmic viscosity changes in cell signaling modulation) 1 and at the organismal level (e.g., blood, plasma, or lymphatic fluid viscosity changes in diabetes, hypertension, infarction, and aging). 2 It has been proposed that monitoring of biofluid viscosity could provide a diagnostic tool for the detection of diseases. 3 Since mechanical devices do not provide the spatial and temporal resolution needed, a new type of fluorescent-based viscosity sensors was developed. 4 These sensors are based on a class of environmentsensitive fluorescent dyes that are characterized by a viscositydependent emission quantum yield. 4,5 The chemical structure of these dyes contains an electron donor unit (such as a nitrogen atom) in conjugation with an electron acceptor unit (such as a nitrile). Upon photoexcitation, the two units can rotate relative to each other in a manner that is dependent on the viscosity of their environment. Representative examples of such fluorescent rotors are 9-(dicyanoVinyl)julolidine (DCVJ, 1) and 2-cyano-3-(4-dimethylaminophenyl)acrylic acid methyl ester (CMAM, 2) ( Figure 1). 5 Their viscosity-dependent fluorescent quantum yield is described by the Förster-Hoffmann equation (eq 1). 6 Fluorescent molecular rotors have been used for viscosity studies that are performed by steady-state fluorescence through emission intensity measurements. This method suffers, however, from drawbacks arising from changes of the fluid optical properties and fluctuations in dye concentrations. An additional disadvantage is that a calibration curve is needed for the absolute determination of viscosity. 5 As a consequence, changes in fluid properties and dye concentration may cause erroneous readings.We hypothesized that a dual dye composed of two distinct fluorescent units, one providing an internal intensity reference and the other acting as a viscosity sensor, would create a ratiometric sensing system, thus overcoming the above disadvantages. Dividing the sensor emission intensity by the reference emission intensity would yield a normalized intensity that should not only eliminate some of the fluid-and concentration-related artifacts but also provide a means to quantify viscosity by an internal reference. To test this hypothesis, we synthesized a compound 4 in which the CMAM motif was coupled with 7-methoxycoumarin-3-carboxylic acid (MCCA, 3). We chose MCCA as the donor fluorophore in order to induce excitation of the rotor moiety (CMAM) via Resonance Energy Transfer (RET). 7 We envisioned that, due to its viscosity-independent quantum yield, MCCA could be used as both the internal reference and the RET donor. The latter event could then excite the CMAM motif, resulting in a viscosity-dependent emission of the rotor. The linker was chosen to maintain a distance between the chromophores in the same range as the Förster distance 7a to allow considerable energy transfer to the acceptor combined w...

The modification of molecular rotors towards increased cell membrane association provides a new research tool for membrane viscosity measurements. The use of these rotors complements established methods such as fluorescence recovery after photobleaching with its limited spatial and temporal resolution and fluorescence anisotropy, which has low sensitivity and may be subject to other effects such as deformation.