Monodispersed Lignin Colloidal Spheres with Tailorable Sizes for Bio-Photonic Materials.

Lignin colloidal spheres (LCSs) are promising biomaterials for application in drug storage and delivery, pollutant adsorption, and ultraviolet protection due to their biocompatibility, amphiphilicity, and conjugated structure. However, wide size distribution of LCSs greatly limits their performances, especially in many precise and advanced applications. Herein, the fabrication of monodispersed LCSs with tailorable sizes ranging from the nanoscale to microscale is reported. Lignin raw materials are first fractionated by solvent extraction, and then the lignin fraction is used to fabricate monodispersed LCSs by solvent/antisolvent self-assembly. The underlying mechanism for the formation of monodispersed LCS is primarily ascribed to the improved homogeneity of long-range intermolecular forces, especially the electrostatic forces and hydrophobic forces, between lignin molecules. Moreover, by manipulating the short-range order of LCSs, an innovative application of lignin as bio-photonic materials with tunable structural colorations (e.g., red, green, or blue) is demonstrated. This work not only provides deep insight and an effective strategy to eliminate the serious inhomogeneity of LCSs, but also makes lignin resources have great potential as biodegradable and biocompatible photonic materials in diverse advanced optical application fields such as photonic devices, anti-counterfeiting labels, and structural color pigments.

Photonic Lignin with Tunable and Stimuli-Responsive Structural Color.

Due to the growing sustainability and health requirements, structural color materials fabricated with functional natural polymers have attracted increasing attention in advanced optical and biomedical fields. Lignin has many attractive features such as great biocompatibility, ultraviolet resistance, antioxidant property, and thermostability, making it a promising natural resource to be fabricated as functional structural color materials. However, to date, the utilization of lignin as the building block for structural color materials is still a challenge due to its disordered structure. Herein, we present a strategy to transform disordered lignin into ordered "photonic lignin", in which monodisperse lignin colloidal spheres are prepared via solvent/antisolvent self-assembly, and then the periodic structure is constructed by centrifugal effect. The photonic lignin exhibits structural colors that are tunable by modulating the diameter of lignin colloidal spheres. We further demonstrate the application of photonic lignin as a natural polymer-based coating that shows bright, angle-independent, and stimuli-responsive structural colors. Moreover, the cytotoxicity assay indicates the excellent biocompatibility of photonic lignin with human skin, blood vessels, digestive systems, and other tissues, which demonstrates the great potential of photonic lignin in the applications such as implanted/wearable optical devices, advanced cosmetics, and smart food packaging.

Spinal CCK1 Receptors Contribute to Somatic Pain Hypersensitivity Induced by Malocclusion via a Reciprocal Neuron-Glial Signaling Cascade.

Recent studies have shown that the incidence of chronic primary pain including temporomandibular disorders (TMD) and fibromyalgia syndrome (FMS) often exhibit comorbidities. We recently reported that central sensitization and descending facilitation system contributed to the development of somatic pain hypersensitivity induced by orofacial inflammation combined with stress. The purpose of this study was to explore whether TMD caused by unilateral anterior crossbite (UAC) can induce somatic pain hypersensitivity, and whether the cholecystokinin (CCK) receptor-mediated descending facilitation system promotes hypersensitivity through neuron-glia cell signaling cascade. UAC evoked thermal and mechanical pain hypersensitivity of the hind paws from day 5 to 70 that peaked at week 4 post UAC. The expression levels of CCK1 receptors, interleukin-18 (IL-18) and IL-18 receptors (IL-18R) were significantly up-regulated in the L4 to L5 spinal dorsal horn at 4 weeks post UAC. Intrathecal injection of CCK1 and IL-18 receptor antagonists blocked somatic pain hypersensitivity. IL-18 mainly co-localized with microglia, while IL-18R mainly co-localized with astrocytes and to a lesser extent with neurons. These findings indicate that the signaling transduction between neurons and glia at the spinal cord level contributes to the descending pain facilitation through CCK1 receptors during the development of the comorbidity of TMD and FMS. PERSPECTIVE: CCK1 receptor-dependent descending facilitation may mediate central mechanisms underlying the development of widespread somatic pain via a reciprocal neuron-glial signaling cascade, providing novel therapeutic targets for the clinical treatment of TMD and FMS comorbidities.

Animal Models of Temporomandibular Disorder.

Temporomandibular disorders (TMD) are a group of diseases in the oral and maxillofacial region that can manifest as acute or chronic persistent pain, affecting millions of people worldwide. Although hundreds of studies have explored mechanisms and treatments underlying TMD, multiple pathogenic factors and diverse clinical manifestations make it still poorly managed. Appropriate animal models are helpful to study the pathogenesis of TMD and explore effective treatment measures. At present, due to the high cost of obtaining large animals, rodents and rabbits are often used to prepare TMD animal models. Over the past decade, various animal models have been intensively developed to understand neurobiological and molecular mechanisms of TMD, and seek effective treatments. Although these models cannot carry out all clinical features, they are valuable in revealing the mechanisms of TMD and creating curative access. Currently, there are multitudinous animal models of TMD research. They can be constructed in different means and summarized into four ways according to the various causes and symptoms, including chemical induction (intra-articular injection of ovalbumin, collagenase, formalin, vascular endothelial growth factor, intramuscular injection of complete Freund's adjuvant, etc.), mechanical stress stimulation (passive mouth opening, change of chewing load), surgical operation (partial disc resection, joint disc perforation) and psychological stress induction. Here, we summarize and discuss different approaches of animal models for determining neurophysiological and mechanical mechanisms of TMD and assess their advantages and limitations, respectively.

Risk Factors for Enterovirus A71 Seropositivity in Rural Indigenous Populations in West Malaysia.

Enterovirus A71 (EV-A71), which is transmitted by the fecal-oral route, causes hand, foot and mouth disease and, rarely, severe neurological complications. In Malaysia, the indigenous rural community (Orang Asli) has a high prevalence of parasitic diseases due to poor sanitation, water supply and hygiene practices. This cross-sectional study compared the seroepidemiology of EV-A71 among rural Orang Asli and urban Kuala Lumpur populations in West Malaysia, and determined the risk factors associated with EV-A71 seropositivity in rural Orang Asli. Seropositive rates were determined by neutralization assay. EV-A71 seropositivity was strongly associated with increasing age in both populations. Rural Orang Asli children ≤12 years had significantly higher EV-A71 seropositivity rates than urban Kuala Lumpur children (95.5% vs 57.6%, P < 0.001), and also higher rates in the age groups of 1-3, 4-6 and 7-12 years. Multivariate analysis confirmed that age ≤12 years (adjusted OR 8.1, 95% CI 3.2-20.7, P < 0.001) and using untreated water (adjusted OR 6.2, 95% CI 2.3-16.6, P < 0.001) were independently associated with EV-A71 seropositivity in the Orang Asli population. Supply of clean drinking water may reduce the risk of EV-A71 infection. With significantly higher EV-A71 seropositive rates, younger rural children should be a priority target for future vaccination programs in Malaysia.