The Permeability to Oxygen of the Periderm of the Potato Tuber

The permeability to oxygen of the periderm of the potato tuberhas been measured during its development and storage. When expressedas ml O₂, diffusing through 1 cm² periderm in 1 sec under anO₂, pressure of 1 atm, the values for freshly harvested tubersranged from a maximum of 2.4 x 10^–4 in immature tubers,to less than 0.7 x 10^–4 in tubers harvested mature someweeks after the death of the foliage. In every case, after storagefor up to 10 weeks at 10^° C, the permeabilities, as expressedabove, were less than 0.7 x 10^–4 (minimum values, c. 0.5x 10^–4 It was shown that the oxygen deficit under theperiderm was unlikely to exceed 0.03 atm during development,and the oxygen status of the developing tuber should thus beadequate for the low oxygen-affinity oxidase system (if present)to function.     

活性氧、线粒体通透性转换与细胞凋亡

线粒体是真核细胞中非常重要的细胞器,细胞中的活性氧等自由基主要来源于此,线粒体膜的通透性转换(mitochondrial permeability transition,MPT)及其孔道(mitochondrialpermeability transition pore,MPTP)更是在内源性细胞凋亡中发挥了关键作用。持续性的线粒体膜通透性转换在凋亡的效应阶段起决定性作用,可介导细胞色素c等促凋亡因子从线粒体释放到胞浆中,进一步激活下游的信号通路,导致细胞不可逆地走向凋亡。瞬时性的线粒体膜通透性转换及其偶联的线粒体局部的活性氧爆发同样具有促凋亡的作用。线粒体通透性孔道的开放释放出大量活性氧,这些活性氧又能够进一步激活该孔道,以正反馈的形式进一步加剧孔道的打开,放大凋亡信号。活性氧、线粒体通透性转换与细胞凋亡之间具有密不可分的联系,本文根据已知的研究结果集中讨论了这三者的关系,并着重论述了该领域中的最新发现和成果。     

The Role of Reactive Oxygen Species in Mitochondrial Permeability Transition

We have provided evidence that mitochondrial membrane permeability transition induced by inorganic phosphate, uncouplers or prooxidants such as t-butyl hydroperoxide and diamide is caused by a Ca²⁺-stimulated production of reactive oxygen species (ROS) by the respiratory chain, at the level of the coenzyme Q. The ROS attack to membrane protein thiols produces cross-linkage reactions, that may open membrane pores upon Ca²⁺ binding. Studies with submitochondrial particles have demonstrated that the binding of Ca²⁺ to these particles (possibly to cardiolipin) induces lipid lateral phase separation detected by electron paramagnetic resonance experiments exploying stearic acids spin labels. This condition leads to a disorganization of respiratory chain components, favoring ROS production and consequent protein and lipid oxidation.     

Microbiological Changes in Prepacked Cod Fillets in Relation to the Oxygen Permeability of the Film

The deterioration of prepacked cod fillets in relation to the oxygen permeability of the polyethylene film was studied bacteriologically and chemically. Spoilage at 0° is not related directly to oxygen permeability (OP). The deterioration curve at higher storage temperatures (3 and 6°) is of the same form as the curve at 0°. Moreover, from the curve it can be deduced that a film with c. 3600 ml/m²/24 h OP gives the best results. A maximum spoilage is observed with an OP c. 1800 ml/m²/24 h. Identical results were obtained with other films. The formation of formalin bound volatile nitrogen compounds is inhibited in prepacked fish whereas the trimethylamine content increases.     

Molecular Mobility and Oxygen Permeability in Amorphous Bovine Serum Albumin Films

We have used phosphorescence from the xanthene probe erythrosin B to characterize the molecular mobility and oxygen permeability as a function of temperature in amorphous solid bovine serum albumin (BSA) films. Analysis of the emission spectrum using a lognormal fitting function provided information on how temperature modulates the emission peak frequency and bandwidth (full width at half maximum). The peak frequency decreased gradually at low and more steeply at high temperature, whereas the bandwidth increased gradually at low and more steeply at high temperature, both changes indicating a softening of the protein matrix at ∼60°C. Phosphorescence intensity decay transients were well fit using a stretched exponential decay function at all temperatures. Lifetimes decreased gradually at low and more steeply at high temperature; Arrhenius analysis of the rate constant for nonradiative collisional quenching indicated an increase in quenching indicative of matrix softening at ∼70°C. The oxygen quenching rate was calculated from a comparison of emission lifetimes in the presence and absence of oxygen. This rate varied linearly with the collisional quenching rate over nearly three orders of magnitude, suggesting that the more global motions that control oxygen translational diffusion are modulated by more local motions that influence collisional quenching of erythrosin. The emission spectrum shifted to higher energy as a function of time following excitation, whereas the phosphorescence lifetime decreased with increasing emission wavelength; both behaviors provided strong evidence for distinct sites within the protein matrix varying in molecular mobility. These results enrich our molecular understanding of the intrinsic mobility of proteins within the amorphous solid phase, provide evidence for a dynamic transition within solid BSA, and provide insight into the molecular mechanisms controlling oxygen diffusion.     

Influence of Chilling on Electrolyte Permeability, Oxygen Uptake and 2,4-Binitrophenol Stimulated Oxygen Uptake in Leaf Discs of the Thermophilic Cucumis sativus

The effect of chilling was studied in leaf discs from the chilling-sensitive Cucumis sativus L. by measurement of the electrolyte leakage from the discs, by oxygen uptake and by uncoupling of respiration with 2,4 dinitrophenol. Short periods of chilling are characterized by minor significant increases of electrolyte permeability, of respiration and of preserved ability to be uncoupled by 2,4-dinilrophenol. A longer period of chilling resulted in a strongly increased electrolyte permeability, in reduced oxygen uptake and in disappearance of uncoupling by 2,4 dinitrophenol. In general the induced changes in permeability and respiration were reversible within 4 days of chilling, if the discs were placed at 25°C after chilling.     

The Role of the Oxygen Permeability of the Seed Coat in the Dormancy of Seed of Xanthium pennsylvanicum Wallr

A method for direct identification and quantitative measurementsof mixed or pure gases diffusing through seed coats was devisedto test the hypothesis that the dormancy of Xanthium pennsylvanicumseeds is caused by oxygen-impermeable seed coats. The diffusionof oxygen through seed coats of X. pennsylvanicum was shownto obey Fick's first law. Oxygen diffused through the lowerand upper seed coats at the same rate. Imbibed lower and upperseeds showed essentially equal oxygen uptake rates before radicleemergence. This uptake was lower than the rate at which oxygencan diffuse into the seed. Therefore upper seeds are not dormantbecause of seed coat restriction of oxygen diffusion. The relationshipsof oxygen with other factors involved in seed dormancy are discussed.     

Structure of the Cornea in Some Cervidae

The structure of the corneas of adult and young reindeer, roedeer and elk was studied. The corneas were strikingly similar in general appearance. The number of squamous cells was found to be the main difference. The thickness of the cornea and that of the membrane of Descemet was found to be greater in older animals.     

Kinetics and Apparent K(m) of Oxygen Cycle under Conditions of Limiting Carbon Dioxide Fixation

A mass spectrometer with a membrane inlet was used to monitor light-driven O₂ evolution, O₂ uptake, and CO₂ uptake in suspensions of algae (Scenedesmus obliquus). We observed the following. (a) The rate of O₂ uptake, which, in the presence of iodoacetamide, replaces the uptake of CO₂, showed a distinct plateau (V_max) beyond ~30% O₂ and was half-maximal at ~8% O₂. We concluded that this light-driven O₂ uptake process, which does not involve carbon compounds, is saturated at lower O₂ concentrations than are photorespiration and glycolate formation. (b) In the absence of inhibitor, O₂ evolution was relatively unaffected by the presence or absence of CO₂. During the course of CO₂ depletion, electron flow to CO₂ was replaced by an equivalent flow to O₂. (c) There was a distinct delay between the cessation of CO₂ uptake and the increase in O₂ uptake. We ascribe this delay to the transient utilization of another electron acceptor—possibly bicarbonate or another bound form of CO₂.     

Influence of Some Preservatives on the Quality of Prepacked Cod Fillets in Relation to the Oxygen Permeability of the Film

S ummary : The deterioration of prepacked cod fillets in relation to different concentrations of citric acid (HC) and of potassium sorbate (PS) was studied bacteriologically and chemically. Spoilage of fish treated with PS in relation to the oxygen permeability (OP) of the polyethylene film was also examined. The trimethylamine (TMA) and formalin bound nitrogen compounds (FBN) formation at 0° in prepacked cod fillets is inhibited by the addition of HC and PS. A concentration of 0·4% of PS in the cod fillets is sufficient to inhibit the TMA production completely. The OP of the film determines the keeping quality of the cod fillets containing 0·4% of PS. The film with the lowest OP gives the best results, since the spoilage of PS treated fish during the first 12 days is exclusively caused by an increase of FBN. The formation of this fraction at 0° is related directly to the OP of the packing film. From the experiments with PS treated cod fillets it can be deduced that a film with a low OP gives the best results.     

Soybean (Glycine max) Nodule Physical Traits Associated with Permeability Responses to Oxygen

Nodule permeability (P) controls the amount of O2 entering the nodule and is an important determinant of N2 fixation. Modulation of water volume in the intercellular spaces of the nodule cortex was hypothesized to change the effective thickness of a diffusion barrier and account for changes in P. This hypothesis was examined by evaluating physical traits of nodules that may affect P. The first test of the hypothesis was to determine whether alterations in P may result in changing both the density and the air space content of nodules as the water content of intercellular spaces was varied. Density of nodules exposed to 21 kPa O2 increased as the time following detachment from the plant increased from 5 to 60 min. Nodules from soybean (Glycine max [L.] Merr.) plants shaded for 48 h had a lower fractional air space content than nodules from control plants. Nodule detachment and prolonged shading decreased P, and the increase in density and decrease in fractional air space content associated with decreased P in these treatments supports the proposed hypothesis. The second test of the hypothesis was to determine whether nodules released water easily in response to water potential gradients. The intrinsic capacitance of nodules determined by pressure-volume analysis was 0.29 MPa-1 and indicated that the tissue can release relatively large amounts of water from the symplast with only small changes in total nodule water potential. Estimates of the bulk modulus of elasticity ranged from 0.91 to 2.60 MPa and indicated a high degree of elasticity. It was concluded that the physical properties of nodules were consistent with P modulation by the release and uptake of intercellular water in the nodule cortex.     

The Regulation of Vascular Endothelial Growth Factor-induced Microvascular Permeability Requires Rac and Reactive Oxygen Species

Vascular permeability is a complex process involving the coordinated regulation of multiple signaling pathways in the endothelial cell. It has long been documented that vascular endothelial growth factor (VEGF) greatly enhances microvascular permeability; however, the molecular mechanisms controlling VEGF-induced permeability remain unknown. Treatment of microvascular endothelial cells with VEGF led to an increase in reactive oxygen species (ROS) production. ROS are required for VEGF-induced permeability as treatment with the free radical scavenger, N-acetylcysteine, inhibited this effect. Additionally, treatment with VEGF caused ROS-dependent tyrosine phosphorylation of both vascular-endothelial (VE)-cadherin and β-catenin. Rac1 was required for the VEGF-induced increase in permeability and adherens junction protein phosphorylation. Knockdown of Rac1 inhibited VEGF-induced ROS production consistent with Rac lying upstream of ROS in this pathway. Collectively, these data suggest that VEGF leads to a Rac-mediated generation of ROS, which, in turn, elevates the tyrosine phosphorylation of VE-cadherin and β-catenin, ultimately regulating adherens junction integrity.Endothelial cells line the inside of blood vessels and serve as a barrier between circulating blood and the surrounding tissues. Endothelial permeability is mediated by two pathways: the transcellular pathway and the paracellular pathway. In the transcellular pathway material passes through the cells, whereas in the paracellular pathway fluid and macromolecules pass between the cells. The paracellular pathway is regulated by the properties of endothelial cell-cell junctions (1–3). Changes in the permeability of this barrier are tightly regulated under normal physiological conditions. However, dysregulated vascular permeability is observed in many life-threatening conditions, including heart disease, cancer, stroke, and diabetes.VEGF² was first discovered as a potent vascular permeability factor that stimulated a rapid and reversible increase in microvascular permeability without damaging the endothelial cell (4, 5). VEGF was later shown to be a selective growth factor for endothelial cells, capable of promoting migration, growth, and survival (6). Considerable progress has been made toward understanding the signaling events by which VEGF promotes growth and survival (7). However, the mechanism through which VEGF promotes microvascular permeability remains incompletely understood.VE-cadherin is an endothelial cell-specific adhesion molecule that connects adjacent endothelial cells (8, 9). While the barrier function of the endothelium is supported by multiple cell-cell adhesion systems, disruption of VE-cadherin is sufficient to disrupt intercellular junctions (9–11). Earlier studies have demonstrated increased permeability both in vitro and in vivo after treatment with VE-cadherin-blocking antibodies (9, 12). Additionally, VE-cadherin is required to prevent disassembly of blood vessel walls (11, 13) and to coordinate the passage of macromolecules through the endothelium (14, 15). Tyrosine phosphorylation may provide the regulatory link, as increased phosphorylation of cadherins and potential dissociation of the cadherin/catenin complex results in decreased cell-cell adhesion and increased permeability (16, 17).Recent evidence has demonstrated that Rac1-induced reactive oxygen species (ROS) disrupt VE-cadherin based cell-cell adhesion (18). The mechanisms by which ROS affect endothelial permeability have not been fully characterized. VEGF has been reported to induce NADPH oxidase activity and induce the formation of ROS (19, 20). A direct link between Rac and ROS in a non-phagocytic cell was shown in 1996, when it was demonstrated that activated Rac1 resulted in the increased generation of ROS in fibroblasts (21). Several studies have subsequently implicated Rac-mediated production of ROS in a variety of cellular responses, in particular in endothelial cells (22, 23). These data suggest that ROS may play a critical role in integrating signals from VEGF and Rac to regulate the phosphorylation of VE-cadherin and ultimately the integrity of the endothelial barrier.In the present study we sought to determine the mechanism by which VEGF regulates microvascular permeability. Our results show that VEGF treatment of human microvascular endothelial cells results in the Rac-dependent production of ROS and the subsequent tyrosine phosphorylation of VE-cadherin and β-catenin. The phosphorylation of VE-cadherin and β-catenin are dependent on Rac and ROS and result in decreased junctional integrity and enhanced vascular permeability.     

Artificial Cornea and the Future of Eye Banking

A report on the construction of functional human corneal equivalent reflects a step towards creation of an artificial cornea. We discuss the current status of supply and demand for corneas for transplanation, and wonder if the creation of an artificial cornea will have an effect on corneal transplantation in the near future     

The Causes of Necrobiosis and Apoptosis of Cornea Epithelial Cells during Primary Acquired Keratoconus Cornea

We studied 56 biopsy samples of conjunctiva and 50 corneal discs excised from 28 patients with acquired keratoconus cornea. The conjunctivas in all biopsy samples showed various stages of immune inflammation. Necrobiotic changes have been revealed in epithelium of the corneal discs going by the pathways of apoptosis—programmed cell death—and oncosis—initial edematic stage of necrobiosis. At the stage of acute inflammation they are due to cytotoxic effect of the lymphocytes, monocytes, and macrophages. Antibody-dependent cytotoxicity mediated by plasma and lymphoid cells predominates at this stage. At the reparative stage of inflammation ischemia, an inductor of apoptosis and oncosis, underlies necrobiotic changes in corneal epithelium.     

Nitrate Effects on Nodule Oxygen Permeability and Leghemoglobin (Nodule Oximetry and Computer Modeling)

Two current hypotheses to explain nitrate inhibition of nodule function both involve decreased O2 supply for respiration in support of N2 fixation. This decrease could result from either (a) decreased O2 permeability (PO) of the nodule cortex, or (b) conversion of leghemoglobin (Lb) to an inactive, nitrosyl form. These hypotheses were tested using alfalfa (Medicago sativa L. cv Weevlchek) and birdsfoot trefoil (Lotus corniculatus L. cv Fergus) plants grown in growth pouches under controlled conditions. Nodulated roots were exposed to 10 mM KNO3 or KCI. Fractional oxygenation of Lb under air (FOLair), relative concentration of functional Lb, apparent PO, and O2-saturated central zone respiration rate were all monitored by nodule oximetry. Apparent PO and FOLair in nitrate-treated nodules decreased to <50% of values for KCI controls within 24 h, but there was no decrease in functional Lb concentration during the first 72 h. In nitrate-treated alfalfa, but not in birdsfoot trefoil, FOLair, apparent PO, and O2-saturated central zone respiration rate decreased during each light period and recovered somewhat during the subsequent dark period. This species difference could be explained by greater reliance on photoreduction of nitrate in alfalfa than in birdsfoot trefoil. Computer simulations extended the experimental results, showing that previously reported decreases in apparent PO of Glycine max nodules with nitrate exposure cannot be explained by hypothetical decreases in the concentration or O2 affinity of Lb.