Publish in Reproductive Biology and Endocrinology – Article processing charges are only paid by those who can afford it

Editorial Electronic journals are the basis of a world of purely electronic scientific communication. Just imagine, no more bookshelves and mountains of disorganized paperwork, no more late nights organizing and searching for articles of interest. For most active research-oriented students and scientists this is already a reality, or will be in the near future. Although most \u27top ranked\u27 traditional journals now offer web access to recent publications, and to less or more of their archives, not everyone has the luxury of access through their university, or has his/her subscription paid for, or can afford to pay US $30–35 for an electronic reprint. Traditionally, journals generated their revenue from individual subscribers, private and/or state owned institutions, page charges from authors, and charges for color illustrations. Consequently, the traditional science publishing industry limited access to scientific publications to scientists in the developed countries while, in many cases, leaving the rest of the world unattended

Innate immune receptor NOD2 mediates LGR5+ intestinal stem cell protection against ROS cytotoxicity via mitophagy stimulation

International audienceThe nucleotide-binding oligomerization domain-containing protein 2 (NOD2) agonist muramyl dipeptide (MDP), a peptidoglycan motif common to all bacteria, supports leucine-rich repeat-containing G protein-coupled receptor 5 (LGR5)+ intestinal stem cell (ISC) survival through NOD2 activation upon an otherwise lethal oxidative stress-mediated signal. However, the underlying protective mechanisms remain unknown. Here, using irradiation as stressor and primarily murine-derived intestinal organoids as a model system, we show that MDP induced a significant reduction of total and mitochondrial reactive oxygen species (ROS) within ISCs, which was associated with mitophagy induction. ATG16L1 knockout (KO) and NOD2 KO organoids did not benefit from the MDP-induced cytoprotection. We confirmed the MDP-dependent induction of ISC mitophagy upon stress in vivo. These findings elucidate the NOD2-mediated mechanism of cytoprotection involving the clearance of the lethal excess of ROS molecules through mitophagy, triggered by the coordinated activation of NOD2 and ATG16L1 by a nuclear factor κB (NF-κB)-independent pathway

Origin of line tension for a Lennard-Jones nanodroplet

The existence and origin of line tension has remained controversial in literature. To address this issue we compute the shape of Lennard-Jones nanodrops using molecular dynamics and compare them to density functional theory in the approximation of the sharp kink interface. We show that the deviation from Young's law is very small and would correspond to a typical line tension length scale (defined as line tension divided by surface tension) similar to the molecular size and decreasing with Young's angle. We propose an alternative interpretation based on the geometry of the interface at the molecular scale

Black hole lasers, a mode analysis

We show that the black hole laser effect discovered by Corley & Jacobson should be described in terms of frequency eigenmodes that are spatially bound. The spectrum contains a discrete and finite set of complex frequency modes which appear in pairs and which encode the laser effect. In addition, it contains real frequency modes that form a continuous set when space is infinite, and which are only elastically scattered, i.e., not subject to any Bogoliubov transformation. The quantization is straightforward, but the calculation of the asymptotic fluxes is rather involved. When the number of complex frequency modes is small, our expressions differ from those given earlier. In particular, when the region between the horizons shrinks, there is a minimal distance under which no complex frequency mode exists, and no radiation is emitted. Finally, we relate this effect to other dynamical instabilities found for rotating black holes and in electric fields, and we give the conditions to get this type of instability.Comment: 19 pages, 3 figures, main changes: new figure and new Sec.6 `conditions for having a laser effect', final version accepted in PR

The N-terminal domains of syntaxin 7 and vti1b form three-helix bundles that differ in their ability to regulate SNARE complex assembly

The SNAREs syntaxin 7, syntaxin 8, vti1b, and endobrevin/VAMP8 function in the fusion of late endosomes. Although the core complex formed by these SNAREs is very similar to the neuronal SNARE complex, it differs from the neuronal complex in that three of the four SNAREs contain extended N-terminal regions of unknown structure and function. Here we show that the N- terminal regions of syntaxin 7, syntaxin 8, and vti1b contain well folded a-helical domains. Multidimensional NAIR spectroscopy revealed that in syntaxin 7 and vti1b, the domains form three-helix bundles resembling those of syntaxin 1, Sso1p, and Vam3p. The three-helix bundle domain of vti1b is the first of its kind identified in a SNARE outside the syntaxin family. Only syntaxin 7 adopts a closed conformation, whereas in vti1b and syntaxin 8, the N-terminal domains do not interact with the adjacent SNARE motifs. Accordingly, the rate of SNARE complex assembly is retarded about 7-fold when syntaxin 7 contains its N-terminal domain, whereas the N-terminal domains of vti1b and syntaxin 8 have no influence on assembly kinetics. We conclude that three-helix bundles represent a common fold for SNARE N- terminal domains, not restricted to the syntaxin family. However, they differ in their ability to adopt closed conformations and thus to regulate the assembly of SNARE complexes