Characterization of enzymatically isolated myocytes from the turtle, Chrysemys picta

Application of an enzymatic cell isolation technique to a turtle heart yielded mononuclear spindle-shaped myocytes. Turtle myocyte morphology revealed a long, thin, tapered cell with an average length of 221± 9.6 μm and an average width of 9.55 ± 0.87 μm. Cell volume was calculated to be 16,248 ± 24,776 μm³ and mean sarcomere length was 2.24 ± 0.09 μm. The Ca⁺²-tolerant myocytes shortened to a degree of 13 ± 6.1% when stimulated in an electric field. Both spontaneous and induced contractions resembled a twitch. Myocyte volume did not vary significantly with the body mass of the turtle.     

Trends in insomnia research for the next decade: a narrative review

Sleep and Biological Rhythms - Insomnia disorder has known striking developments over the last few years. Partly due to advances in neuroimaging techniques and brain sciences, our understanding of...     

A quantitative and interspecific test for biological activity of anti-müllerian hormone: the fetal ovary aromatase assay.

Anti-Müllerian hormone (AMH), also known as Müllerian-inhibiting substance or factor, has previously been shown to sex-reverse the steroidogenic pattern of fetal mammalian ovaries through repression of aromatase biosynthesis. Study of the ontogeny of the response of cyclic AMP-stimulated aromatase activity of rat fetal ovaries to AMH has allowed us to develop a quantitative bioassay for the hormone. Linear responses as a function of the logarithm of AMH concentration were observed over ranges of 0.2-7.5 micrograms/ml for the bovine protein and 0.15-2 micrograms/ml for the human protein, with a maximal decrease in aromatase activity of 90% for both proteins. Under the same in vitro conditions, AMH treatment did not affect cyclic AMP-stimulated fetal rat testicular aromatase activity. Partially purified chick AMH also decreased rat ovarian aromatase activity, allowing us to use this test to study AMH ontogeny in chick gonads. Analysis of the species specificity of AMH repression of ovarian aromatase activity indicated that turtle and rat fetal ovaries responded to AMH of other vertebrate classes, whereas aromatase activity of chick embryo ovaries could be repressed only by the homospecific hormone.     

Analysis of the correlations for stochastic multicompartmental systems

The covariances among the populations of distinct compartments are studied for the multi-compartmental birthless death-migration-immigration process. The important role played by the transition matrix of the deterministic process is underlined. Several examples are discussed. Work performed under the auspices of the GNFM-CNR.     

Glycosphingolipid metabolic reprogramming drives neural differentiation

Neural development is accomplished by differentiation events leading to metabolic reprogramming. Glycosphingolipid metabolism is reprogrammed during neural development with a switch from globo‐ to ganglio‐series glycosphingolipid production. Failure to execute this glycosphingolipid switch leads to neurodevelopmental disorders in humans, indicating that glycosphingolipids are key players in this process. Nevertheless, both the molecular mechanisms that control the glycosphingolipid switch and its function in neurodevelopment are poorly understood. Here, we describe a self‐contained circuit that controls glycosphingolipid reprogramming and neural differentiation. We find that globo‐series glycosphingolipids repress the epigenetic regulator of neuronal gene expression AUTS2. AUTS2 in turn binds and activates the promoter of the first and rate‐limiting ganglioside‐producing enzyme GM3 synthase, thus fostering the synthesis of gangliosides. By this mechanism, the globo–AUTS2 axis controls glycosphingolipid reprogramming and neural gene expression during neural differentiation, which involves this circuit in neurodevelopment and its defects in neuropathology.