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The use of decellularized tissues or organs as cell culture scaffolds has proven to be a promising approach for tissue engineering and regenerative medicine, as these decellularized tissues can provide the instructive niche for cell differentiation and functions. Cartilage is a largely avascular tissue with limited regenerative capacity. Lesions caused by arthritis can lead to severe cartilage degeneration. Previous studies have indicated that decellularized cartilage can be used as scaffolds that support the chondrogenic differentiation of adult stem cells. However, these decellularization protocols all require the use of denaturing agents, such as high salt and detergents, that lead to the artifactual disruption of the chemical and physical integrity of the tissue microenvironment. Here, we established a new decellularization method for cartilage, through a combined effect of freezing-thawing, sectioning, and sonication in water. This protocol achieved the complete removal of cells within minutes, instead of hours or days required by existing procedures, and does not use any detergent. The resulting decellularized cartilage preserved the native ultrastructure and biochemical contents, including glycosaminoglycans, which is typically depleted by traditional decellularization methods. Human mesenchymal stem cells could readily adhere onto the decellularized cartilage. Together, this work unveils a simple new method for decellularizing cartilage, which will be useful in studying how tissue microenvironment supports chondrocyte growth and functions. Impact statement In this study, we develop a simple, fast cartilage decellularization method that does not require any detergent, so that the decellularized cartilage chemistry is preserved. Traditional detergent-based decellularization removes the tissue biochemical contents (i.e., glycosaminoglycans). In this new water decellularization protocol, the biochemical contents of cartilage can be preserved. This allows the study of biochemistry and physical content in extracellular matrix as a whole, and this protocol would definitely be useful for studying the effect of tissue microenvironment in supporting chondrocyte growth and functions.

A series of substituted 9-methylenylanthracene photocages for diphenylphosphinothioesters have been synthesized to explore their photo-uncaging properties by visible light. Substituents such as phenyl, p-trifluoromethylphenyl, p-methoxyphenyl, ethyn-1-ylbenzene, and 3,3-dimethylbut-1-yn-1-yl have been introduced in order to extend the π-conjugation of the photocage and to shift the wavelength response of the uncaging process to the visible spectral range. Among these new photocages, the (10-(3,3-dimethylbut-1-yn-1-yl)anthracen-9-yl)methyl has been shown to have the best performance in terms of fast photo-uncaging and minimal byproduct formation. It is responsive to both UV and visible photoexcitation. Quantum yields of the photoinduced heterolytic anthracenylmethyl-phosphorus bond cleavage at 366 and 416 nm were found to be 0.08 and 0.025, respectively. This photocage enables traceless Staudinger ligation to be triggered by photoirradiation in the visible spectral range for bioconjugation applications. We demonstrate this with a series of visible-light-induced oligopeptide syntheses via the conjugation of amino acid/oligopeptide building blocks by the characteristic peptide linkage attained by traceless Staudinger ligation. Yields of the resultant conjugated oligopeptides ranged from 31 to 43%. This new photocage opens up the possibility of in situ synthesis of functional proteins/peptides mediated by visible-light-induced photoclick processes for the regulation of cellular/metabolic functions of life systems.

This study aimed to examine the relationship between trait loneliness and diurnal rhythms of salivary cortisol. Fifty-One Chinese undergraduates provided six saliva samples on a weekday at immediately, 0.5, 3, 6, and 12 h after waking, and at bedtime. Saliva collection times were monitored using electronic devices (MEMS TrackCaps). Participants were also administered a questionnaire consisting of scales measuring, trait loneliness, depression, and demographics. Relationships between loneliness and the cortisol awakening response (CAR), diurnal slope (DS), and area under the curve with respect to ground (AUCG) were examined using multiple regression analyses. Results showed that a higher loneliness score was associated with an attenuated CAR, a large AUCG, and a steeper DS, with the effects of compliance, waking time, and depression being controlled. As a blunted CAR and a higher diurnal cortisol level have been shown to be associated with poorer health in prior studies, increased attention to the mechanisms translating loneliness into disease endpoints via elevated cortisol is warranted.

By virtue of the specific amalgam of mercury with gold and high specific area of a graphene scaffold, an environment-friendly multifunctional graphene–gold nanocomposite (G-AuNPs) has been identified and prepared by a simple one-pot redox reaction. The resultant G-AuNPs can reversibly enrich about 94% of Hg2+ in water samples, which can be further separated by only a simple filtration. Importantly, the color of the G-AuNPs suspension exclusively changes from purple–red to light brown upon the addition of Hg2+ in the presence of ascorbic acid, which can be applied for colorimetric detection of Hg2+ with a detection limit (3σ, n = 20) of 1.6 × 10–8 mol·L–1. Furthermore, using ascorbic acid as reducing agents, both the preparation process and the resultant nanocomposite are nontoxic. To the best of our knowledge, this is the first report to enrich, separate and detect Hg2+ contaminant simultaneously without causing any secondary pollution.

By virtue of the specific amalgam of mercury with gold and high specific area of a graphene scaffold, an environment-friendly multifunctional graphene-gold nanocomposite (G-AuNPs) has been identified and prepared by a simple one-pot redox reaction. The resultant G-AuNPs can reversibly enrich about 94% of Hg(2+) in water samples, which can be further separated by only a simple filtration. Importantly, the color of the G-AuNPs suspension exclusively changes from purple-red to light brown upon the addition of Hg(2+) in the presence of ascorbic acid, which can be applied for colorimetric detection of Hg(2+) with a detection limit (3σ, n = 20) of 1.6 × 10(-8) mol·L(-1). Furthermore, using ascorbic acid as reducing agents, both the preparation process and the resultant nanocomposite are nontoxic. To the best of our knowledge, this is the first report to enrich, separate and detect Hg(2+) contaminant simultaneously without causing any secondary pollution.