排序方式: 共有36条查询结果,搜索用时 31 毫秒
31.
Lysophospholipids inhibited mitochondrial Ca2+ uptake, induced a net Ca2+ efflux, and thereby increased the extramitochondrial Ca2+ concentration. The inhibitory potency decreased in the order lysophosphatidylcholine (LPC) = lysophosphatidylglycerol (LPG) greater than lysophosphatidylinositol (LPI) greater than lysophosphatidylserine (LPS) much greater than lysophosphatidylethanolamine (LPE). This relative order is in inverse relation to the ability of the various phospholipid head-groups to build up intermolecular hydrogen bonds with neighbouring membrane lipids. This indicates that changes in Ca2+ transport induced by lysophospholipids are mediated by the interaction of the lysophospholipids with the mitochondrial membrane bilayer structure. The mitochondrial membrane potential, which is the main driving force for mitochondrial Ca2+ uptake, was affected in the same order by the various lysophospholipids. This reduction of the mitochondrial membrane potential may be the underlying cause for the inhibition of the mitochondrial Ca2+ uniport and the resulting release of Ca2+ from the mitochondria. 相似文献
32.
Alton G; Hasilik M; Niehues R; Panneerselvam K; Etchison JR; Fana F; Freeze HH 《Glycobiology》1998,8(3):285-295
Direct utilization of mannose for glycoprotein biosynthesis has not been
studied because cellular mannose is assumed to be derived entirely from
glucose. However, animal sera contain sufficient mannose to force uptake
through glucose-tolerant, mannose-specific transporters. Under
physiological conditions this transport system provides 75% of the mannose
for protein glycosylation in human hepatoma cells despite a 50- to 100-fold
higher concentration of glucose. This suggests that direct use of mannose
is more important than conversion from glucose. Consistent with this
finding the liver is low in phosphomannose isomerase activity
(fructose-6-P<->mannose-6-P), the key enzyme for supplying
glucose-derived mannose to the N-glycosylation pathway. [2- 3H] Mannose is
rapidly absorbed from the intestine of anesthetized rats and cleared from
the blood with a t1/2of 30 min. After a 30 min lag, label is incorporated
into plasma glycoproteins, and into glycoproteins of all organs during the
first hour. Most (87%) of the initial incorporation occurs in the liver,
but this decreases as radiolabeled plasma glycoproteins increase.
Radiolabel in glycoproteins also increases 2- to 6-fold in other organs
between 1-8 h, especially in lung, skeletal muscle, and heart. These organs
may take up hepatic- derived radiolabeled plasma glycoproteins.
Significantly, the brain, which is not exposed to plasma glycoproteins,
shows essentially no increase in radiolabel. These results suggest that
mammals use mannose transporters to deliver mannose from blood to the liver
and other organs for glycoprotein biosynthesis. Additionally, contrary to
expectations, most of the mannose for glycoprotein biosynthesis in cultured
hepatoma cells is derived from mannose, not glucose. Extracellular mannose
may also make a significant contribution to glycoprotein biosynthesis in
the intact organism.
相似文献
33.
The phylogeny and substitution rates of the mammalian X chromosome- located
and autosomal phosphoglycerate kinase and pyruvate dehydrogenase genes were
investigated. Compatibility analysis was used to show reticulate evolution
in these genes. Analysis of the marsupial, mouse, and human
phosphoglycerate kinase genes suggests that at least two recombination
events have taken place, one occurring about the time of the
placental-marsupial split involving exons 1-5 and the other before the
primate-rodent split involving exons 9-10. Similar analysis of the pyruvate
dehydrogenase genes indicates a recombination event involving exons 2-3 at
a time before the primate-rodent split and a gene conversion between exons
3-4 in the human somatic and testis- specific pyruvate dehydrogenase genes
after the primate-rodent split. This demonstrates that genetic exchange can
occur between paralogous genes at widely separated chromosomal locations.
Estimation of nucleotide substitution rates in these genes confirmed a
higher substitution rate in the pyruvate dehydrogenase genes. In the
phosphoglycerate kinase genes, there is no difference between the
substitution rates in mice and humans and between the X chromosome- and
autosome-located genes. A greater substitution rate was noted in the mouse
autosomal pyruvate dehydrogenase gene when compared with the other mouse
and human genes. This may be a result of either directional natural
selection or a relaxation of functional constraint at this specific gene.
相似文献
34.
The immediate reaction products of PLA2-mediated hydrolysis of phospholipids were tested for their ability to induce Ca2+ mobilization from internal stores in permeabilized ob/ob mouse pancreatic islets. Lysophospholipids and unsaturated fatty acids increased the free Ca2+ concentration in the incubation medium of permeabilized ob/ob mouse pancreatic islets. The potency of the lysophospholipids decreased in the following order: lysophosphatidylcholine = lysophosphatidylglycerol much greater than lysophosphatidylinositol greater than lysophosphatidylserine much greater than lysophosphatidylethanolamine. Arachidonic acid and palmitoleic acid had a potency comparable to lysophosphatidylinositol, while palmitic acid was ineffective. The Ca(2+)-mobilizing effect of inositol-1,4,5-trisphosphate (IP3) in permeabilized islet cells was additive to the lysophospholipid effect, indicating different sites of action. Both Ca(2+)-mobilizing effects were counteracted by the polyamine spermine, while the presence of Mg2+ shifted the Ca2+ concentrations to higher levels. Since not only an activation of a phospholipase C but also an activation of a phospholipase A2 with subsequent generation of lysophospholipids and free fatty acids is reported to occur in glucose-induced insulin secretion, the interaction of the phospholipase C reaction product IP3 with a lysophospholipid or an unsaturated fatty acid may affect the extent and duration of the rise in the free cytoplasmic Ca2+ concentration responsible for initiation of insulin secretion. 相似文献
35.
Background
Despite its clinical importance, a dearth of information exists on the cellular and molecular mechanisms that underpin brain stem death. A suitable neural substrate for mechanistic delineation on brain stem death resides in the rostral ventrolateral medulla (RVLM) because it is the origin of a life-and-death signal that sequentially increases (pro-life) and decreases (pro-death) to reflect the advancing central cardiovascular regulatory dysfunction during the progression towards brain stem death in critically ill patients. The present study evaluated the hypothesis that heme oxygnase-1 (HO-1) may play a pro-life role as an interposing signal between hypoxia-inducible factor-1 (HIF-1) and nitric oxide synthase I (NOS I)/protein kinase G (PKG) cascade in RVLM, which sustains central cardiovascular regulatory functions during brain stem death. 相似文献36.