ATPase activity of guinea pig heart muscle

Riassunto L'Autore ha studiato l'influenza della concentrazione degli ioni Ca⁺⁺ e Mg⁺⁺ sull'ATPasi degli atri e dei ventricoli di cuore di cavia. Tale attività è maggiore a pH 9,2 che a pH 6,8. Mentre il Ca⁺⁺ influisce differenziando decisamente le attività degli atri da quelle dei ventricoli, il Mg⁺⁺ accentua piuttosto una differenza tra la parte destra e la sinistra. Il calore distrugge quasi completamente l'attività enzimatica dopo una permanenza a 60° per 20 min.     

Evolution of the extracellular space in immature nervous tissue

Resumen En el cerebelo de rata recién nacida existen espacios extracelulares mayores que 1000 Å los cuales progresivamente se reducen hasta que en la tercera semana, como en el adulto, las celulas y fibras se hallan separadas por endiduras de 150–200 Å. Estas observaciones indican que el reducido espacio usualmente hallado en el adulto no es un artificio tecnico como ha sido sugerido por algunos autores.     

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

Human chromosome 2 is unique to the human lineage in being the product of a head-to-head fusion of two intermediate-sized ancestral chromosomes. Chromosome 4 has received attention primarily related to the search for the Huntington's disease gene, but also for genes associated with Wolf-Hirschhorn syndrome, polycystic kidney disease and a form of muscular dystrophy. Here we present approximately 237 million base pairs of sequence for chromosome 2, and 186 million base pairs for chromosome 4, representing more than 99.6% of their euchromatic sequences. Our initial analyses have identified 1,346 protein-coding genes and 1,239 pseudogenes on chromosome 2, and 796 protein-coding genes and 778 pseudogenes on chromosome 4. Extensive analyses confirm the underlying construction of the sequence, and expand our understanding of the structure and evolution of mammalian chromosomes, including gene deserts, segmental duplications and highly variant regions.     

Structures of ParB bound to DNA reveal mechanism of partition complex formation

The faithful inheritance of genetic information, which is essential for all organisms, requires accurate DNA partition (segregation) at cell division. In prokaryotes, partition is mediated by par systems, for which the P1 plasmid system of Escherichia coli is a prototype comprising a partition site and two proteins, ParA and ParB. To form the partition complex necessary for segregation, P1 ParB must recognize a complicated arrangement of A-box and B-box DNA motifs located on opposite ends of a sharply bent parS partition site of approximately 74 bp (refs 3-7). Here we describe structures of ParB bound to partition sites. ParB forms an asymmetric dimer with extended amino-terminal HTH (helix-turn-helix) domains that contact A-boxes. The two HTH domains emanate from a dimerized DNA-binding module composed of a six-stranded beta-sheet coiled-coil that binds B-boxes. Strikingly, these individual DNA-binding modules rotate freely about a flexible linker, enabling them to contact several arrangements of A- and B-boxes. Most notably, each DNA-binding element binds to and thus bridges adjacent DNA duplexes. These unique structural features of ParB explain how this protein can bind complex arrays of A- and B-box elements on adjacent DNA arms of the looped partition site.     

Effect of heat-labile enterotoxin (LT) produced byEscherichia coli on in vitro cell proliferation

Summary Filtrates fromE. coli H10407 cultures, giving a positive response for heat-labile enterotoxin (LT) in the Y-1 cell test, show an inhibitory activity both on³H-thymidine uptake by Ehrlich ascites cells and on granulocytic-macrophagic precursors (CFU-C) in murine bone marrow.Acknowledgments. We gratefully acknowledge the expert technical assistance of L. Basso and A. Gerosa of Department of Pathology, Hospital of Desio.     

Selective destruction in testes induced by fluoroacetamide

Riassunto Gli autori descrivono le lesioni del testicolo del ratto osservate nel corso di sperimentazioni con la fluoroacetamide. Tali lesioni consistono in alterazioni regressive interessanti elettivamente la linea seminale.     

Polyamines and nucleic acids in rat liver subjected to ionizing radiation

Riassunto Un considerevole aumento di spermina e spermidina è stato osservato nel fegato di ratti dopo 48 h dalla pan-irradiazione con dosi totali di raggi X di 800 e di 1000 r. Gli acidi ribonucleici si modificano nello stesso modo, quantunque in misura minore.     

Cardiac angiogenic imbalance leads to peripartum cardiomyopathy

Peripartum cardiomyopathy (PPCM) is an often fatal disease that affects pregnant women who are near delivery, and it occurs more frequently in women with pre-eclampsia and/or multiple gestation. The aetiology of PPCM, and why it is associated with pre-eclampsia, remain unknown. Here we show that PPCM is associated with a systemic angiogenic imbalance, accentuated by pre-eclampsia. Mice that lack cardiac PGC-1α, a powerful regulator of angiogenesis, develop profound PPCM. Importantly, the PPCM is entirely rescued by pro-angiogenic therapies. In humans, the placenta in late gestation secretes VEGF inhibitors like soluble FLT1 (sFLT1), and this is accentuated by multiple gestation and pre-eclampsia. This anti-angiogenic environment is accompanied by subclinical cardiac dysfunction, the extent of which correlates with circulating levels of sFLT1. Exogenous sFLT1 alone caused diastolic dysfunction in wild-type mice, and profound systolic dysfunction in mice lacking cardiac PGC-1α. Finally, plasma samples from women with PPCM contained abnormally high levels of sFLT1. These data indicate that PPCM is mainly a vascular disease, caused by excess anti-angiogenic signalling in the peripartum period. The data also explain how late pregnancy poses a threat to cardiac homeostasis, and why pre-eclampsia and multiple gestation are important risk factors for the development of PPCM.