Boston University

About: Boston University is a education organization based out in Boston, Massachusetts, United States. It is known for research contribution in the topics: Population & Poison control. The organization has 48688 authors who have published 119622 publications receiving 6276020 citations. The organization is also known as: BU & Boston U.

Disruption of coordinated cardiac hypertrophy and angiogenesis contributes to the transition to heart failure

Abstract: Although increased external load initially induces cardiac hypertrophy with preserved contractility, sustained overload eventually leads to heart failure through poorly understood mechanisms. Here we describe a conditional transgenic system in mice characterized by the sequential development of adaptive cardiac hypertrophy with preserved contractility in the acute phase and dilated cardiomyopathy in the chronic phase following the induction of an activated Akt1 gene in the heart. Coronary angiogenesis was enhanced during the acute phase of adaptive cardiac growth but reduced as hearts underwent pathological remodeling. Enhanced angiogenesis in the acute phase was associated with mammalian target of rapamycin-dependent induction of myocardial VEGF and angiopoietin-2 expression. Inhibition of angiogenesis by a decoy VEGF receptor in the acute phase led to decreased capillary density, contractile dysfunction, and impaired cardiac growth. Thus, both heart size and cardiac function are angiogenesis dependent, and disruption of coordinated tissue growth and angiogenesis in the heart contributes to the progression from adaptive cardiac hypertrophy to heart failure.

Constraints from Thorium/Lanthanum on Sediment Recycling at Subduction Zones and the Evolution of the Continents

Abstract: Arc magmas and the continental crust share many chemical features, but a major question remains as to whether these features are created by subduction or are recycled from subducting sediment. This question is explored here using Th/La, which is low in oceanic basalts ( 0·25) and varies in arc basalts and marine sediments (0·09–0·34). Volcanic arcs form linear mixing arrays between mantle and sediment in plots of Th/La vs Sm/La. The mantle end-member for different arcs varies between highly depleted and enriched compositions. The sedimentary end-member is typically the same as local trench sediment. Thus, arc magmas inherit their Th/La from subducting sediment and high Th/La is not newly created during subduction (or by intraplate, adakite or Archaean magmatism). Instead, there is a large fractionation in Th/La within the continental crust, caused by the preferential partitioning of La over Th in mafic and accessory minerals. These observations suggest a mechanism of ‘fractionation & foundering’, whereby continents differentiate into a granitic upper crust and restite-cumulate lower crust, which periodically founders into the mantle. The bulk continental crust can reach its current elevated Th/La if arc crust differentiates and loses 25–60% of its mafic residues to foundering.

Subcellular localization of the b-cytochrome component of the human neutrophil microbicidal oxidase: translocation during activation.

Abstract: We describe a new method for subcellular fractionation of human neutrophils. Neutrophils were disrupted by nitrogen cavitation and the nuclei removed by centrifugation. The postnuclear supernatant was applied on top of a discontinuous Percoll density gradient. Centrifugation for 15 min at 48,000 g resulted in complete separation of plasma membranes, azurophil granules, and specific granules. As determined by ultrastructure and the distribution of biochemical markers of these organelles, approximately 90% of the b-cytochrome in unstimulated cells was recovered from the band containing the specific granules and was shown to be in or tightly associated with the membrane. During stimulation of intact neutrophils with phorbol myristate acetate or the ionophore A23187, we observed translocation of 40-75% of the b-cytochrome to the plasma membrane. The extent of this translocation closely paralleled release of the specific granule marker, vitamin B12-binding protein. These data indicate that the b-cytochrome is in the membrane of the specific granules of unstimulated neutrophils and that stimulus-induced fusion of these granules with the plasma membrane results in a translocation of the cytochrome. Our observations provide a basis for the assembly of the microbicidal oxidase of the human neutrophil.