Atomic force microscopy-single-molecule force spectroscopy unveils GPCR cell surface architecture.

G protein-coupled receptors (GPCRs) form the largest family of cell surface receptors. Despite considerable insights into their pharmacology, the GPCR architecture at the cell surface still remains largely unexplored. Herein, we present the specific unfolding of different GPCRs at the surface of living mammalian cells by atomic force microscopy-based single molecule force spectroscopy (AFM-SMFS). Mathematical analysis of the GPCR unfolding distances at resting state revealed the presence of different receptor populations relying on distinct oligomeric states which are receptor-specific and receptor expression-dependent. Moreover, we show that the oligomer size dictates the receptor spatial organization with nanoclusters of high-order oligomers while lower-order complexes spread over the whole cell surface. Finally, the receptor activity reshapes both the oligomeric populations and their spatial arrangement. These results add an additional level of complexity to the GPCR pharmacology until now considered to arise from a single receptor population at the cell surface.

A role for mesenchyme dynamics in mouse lung branching morphogenesis.

Mammalian airways are highly ramified tree-like structures that develop by the repetitive branching of the lung epithelium into the surrounding mesenchyme through reciprocal interactions. Based on a morphometric analysis of the epithelial tree, it has been recently proposed that the complete branching scheme is specified early in each lineage by a programme using elementary patterning routines at specific sites and times in the developing lung. However, the coupled dynamics of both the epithelium and mesenchyme have been overlooked in this process. Using a qualitative and quantitative in vivo morphometric analysis of the E11.25 to E13.5 mouse whole right cranial lobe structure, we show that beyond the first generations, the branching stereotypy relaxes and both spatial and temporal variations are common. The branching pattern and branching rate are sensitive to the dynamic changes of the mesoderm shape that is in turn mainly dependent upon the volume and shape of the surrounding intrathoracic organs. Spatial and temporal variations of the tree architecture are related to local and subtle modifications of the mesoderm growth. Remarkably, buds never meet after suffering branching variations and continue to homogenously fill the opening spaces in the mesenchyme. Moreover despite inter-specimen variations, the growth of the epithelial tree and the mesenchyme remains highly correlated over time at the whole lobe level, implying a long-range regulation of the lung lobe morphogenesis. Together, these findings indicate that the lung epithelial tree is likely to adapt in real time to fill the available space in the mesenchyme, rather than being rigidly specified and predefined by a global programme. Our results strongly support the idea that a comprehensive understanding of lung branching mechanisms cannot be inferred from the branching pattern or behavior alone. Rather it needs to be elaborated upon with the reconsideration of mesenchyme-epithelium coupled growth and lung tissues mechanics.

Asymptotic distribution of the "orthogonal" quantitative transmission disequilibrium test in a structured population: exact formula.

Population structure is a recurrent problem for the detection of associations between a marker and a trait, because it can lead to an excess of false positives of the association tests. One popular way of circumventing this problem is the use of family based tests, which consider the transmission of the genotype from the parents to the offspring. Here we focus on quantitative traits and study the Abecasis "orthogonal" quantitative transmission disequilibrium test, which is commonly used in family based association studies. We derive the probability distribution of this test under a general model of structured population. Our derivations show that this test leads to a small excess of false positives due to population structure. They also illustrate and quantify how the heterogeneity in genotypes and phenotypes between populations affect the power of the test. We finally show that the excess of false positives observed for the Abecasis "orthogonal" test may also be found for the Allison "linear" test, though at a lower extent.

Spatial and temporal distribution of cholera in Ecuador between 1991 and 1996.

BACKGROUND: The seventh pandemic of cholera affected South America in 1991 after a century of absence. Favoured by local conditions, the epidemic of cholera in Ecuador had a rapid impact. The epidemic of cholera evolved with temporal and geographical variations. METHODS: The temporal and geographical variations of cholera in Ecuador between 1991 and 1996 have been analysed. The Ecuadorian epidemiological surveillance system is a semi-active one based on obligatory weekly declarations. A geographical representation of annual impact rate has been made. Using a smoothing technique by cross-validation, time curves were identified and spatial diffusion was studied by cartography. RESULTS: In 1991 and 1992, cholera in Ecuador evolved in an epidemic mode with two explosive epidemic peaks. Cholera then entered a phase of regression. The disease spread from two main epicentres, one in the South (El Oro, Guayas, Los Rios) and the other in the North (Esmeraldas and Imbabura). These focal outbreaks spread to neighbouring provinces during the peak outbreaks between 1991 and 1993. CONCLUSION: This study demonstrated that the epidemic spread from the affected provinces in the South and the North of the country.