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J. Biol. Chem., Vol. 275, Issue 51, 39807-39810, December 22, 2000

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ACCELERATED PUBLICATION
Ca²⁺- and Phosphatidylinositol 3-Kinase-dependent Nitric Oxide Generation in Lung Endothelial Cells in Situ with Ischemia^*

Abu B. Al-Mehdi, Chun Song, Kasumi Tozawa, and Aron B. Fisher^§

From the Institute for Environmental Medicine, University of Pennsylvania, Philadelphia, Pennsylvania 19104

Received for publication, October 4, 2000

	ABSTRACT

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS AND DISCUSSION REFERENCES

Endothelial cells generate nitric oxide (NO) in response to agonist stimulation or increased shear stress. In this study, we evaluated the effects of abrupt cessation of shear stress on pulmonary endothelial NO generation and its relationship to changes in intracellular Ca²⁺. In situ endothelial generation of NO and changes in intracellular Ca²⁺ in isolated, intact rat lungs were evaluated using fluorescence microscopy with diaminofluorescein diacetate, an NO probe, and Fluo-3, a Ca²⁺ probe. The onset of increased NO generation in endothelial cells of subpleural microvessels in situ occurred between 30 and 90 s after onset of ischemia and was preceded by an increase in intracellular Ca²⁺ due to both influx of extracellular Ca²⁺ and release from intracellular stores. Flow cessation-induced NO generation in endothelial cells in situ was Ca²⁺-, calmodulin-, and PI3-kinase-dependent. The similarity of endothelial cell response (increased NO generation) to either increased flow or cessation of flow suggests that cells respond to an imposed alteration from a state of adaptation. This response to flow cessation may constitute a compensatory vasodilatatory mechanism and may play a role in signaling for cell proliferation and vascular remodeling.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS AND DISCUSSION REFERENCES

Nitric oxide (NO)¹ is a potent regulator of vascular tone in systemic and pulmonary vessels and plays an important role in cellular signaling and respiration (1-4). This mediator is generated by endothelial cells in response to agonist stimulation and also as a response to increased shear stress (5). Although the effect of increase in flow on endothelial cell NO generation has been characterized, the effect of abrupt cessation of shear stress (i.e. acute ischemia as in pulmonary embolism or donor lung isolation for transplantation) on pulmonary endothelial NO generation in situ is unknown.

Endothelial cells in situ are constantly exposed to shear stress associated with blood flow and thus become flow-adapted. These cells respond with an increase in cytosolic Ca²⁺ and generation of reactive oxygen species when flow is stopped but oxygenation is maintained (6, 7). A similar response with reactive oxygen species generation subsequent to the abrupt cessation of flow has been demonstrated with endothelial cells adapted to flow in vitro (8). We hypothesized that the basis for this early response is mechanotransduction related to removal of endothelial cell shear stress (9). Increased intracellular Ca²⁺ is known to activate endothelial nitric-oxide synthase (eNOS) resulting in increased NO generation and has been demonstrated in cells exposed to increased shear stress (10, 11). In these nonadapted endothelial cells, shear-stress-induced NOS activation was biphasic, with an initial Ca²⁺-dependent phase and a second, sustained phase that was Ca²⁺-independent and phosphorylation-dependent (10-12). In this study, we evaluated whether the increased intracellular Ca²⁺ associated with the early response to flow cessation leads to increased NO generation. This paradigm constitutes a model for the response to acute ischemia. We have used the term oxygenated ischemia to refer to the abrupt cessation of flow in pulmonary circulation where oxygenation remains adequate during ischemia because of the lung alveolar air, and an analogous effect should apply to the initial several minutes of ischemia in a systemic vessel prior to critical oxygen depletion. Our studies show that in air-ventilated, isolated, intact rat lungs, endothelial cells in situ respond to removal of flow with increased generation of NO.

	EXPERIMENTAL PROCEDURES

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS AND DISCUSSION REFERENCES

We have used an established fluorescence microscopic technique for visualization of subpleural endothelium in situ in isolated, ventilated, and perfused rat lungs to monitor endothelial cell Ca²⁺ and NO (6, 7, 9). NO generation was monitored by labeling the pulmonary endothelium with 4,5-diaminofluorescein diacetate (DAF-2 DA, Calbiochem) that is de-esterified intracellularly to DAF-2. NO and its higher oxides, such as NO_x or nitrous anhydride (N₂O₃), provide the third nitrogen to form a triazo ring from the two amino groups of the nonfluorescent DAF-2 and convert it to diaminotriazolofluorescein (DAF-2T) that is monitored at 490 nm excitation and 530 nm emission (13). Changes in intracellular Ca²⁺ levels were monitored with Fluo-3 acetoxymethyl ester.

Materials-- DAF-2 DA and N^G-nitro-L-arginine methyl ester (L-NAME) were obtained from Calbiochem (La Jolla, CA). Fluo-3/AM and DiI-acetylated LDL were from Molecular Probes (Eugene, OR).

Isolated Lung Perfusion and Intact Organ Endothelial Cell Microscopy-- We used an established intact organ microscopy technique to image microvascular endothelial cells in situ in isolated, ventilated, blood-free rat lungs in real time using an epifluorescence microscope (6, 7, 9). Briefly, Sprague-Dawley male rats (Charles River Breeding Laboratories, Kingston, NY) weighing 150-200 g were anesthetized with intraperitoneal sodium pentobarbital (50 mg/kg). A tracheostomy was performed, and artificial ventilation with 95% air + 5% CO₂ (BOC Group, Inc., Murray Hill, NJ) was started through a cannula. The abdomen was opened and the animal was exsanguinated by transection of major abdominal vessels. A cannula was inserted into the main pulmonary artery via a puncture in the right ventricle, and another was inserted into the left atrium. The lung was cleared of blood by gravity perfusion via the pulmonary artery with an artificial medium (Krebs-Ringer bicarbonate buffer KRB: NaCl, 118.45; KCl, 4.74; MgSO₄/7H₂O, 1.17; CaCl₂/2H₂O, 1.27; KH₂PO₄, 1.18; and NaHCO₃, 24.87 in mmol/liter with 5% dextran and 10 mM glucose at pH 7.4). The flow-through perfusate left the lung via the left atrial cannula. Once the lung became visibly cleared of blood (appeared white in color), the heart-lung preparation was dissected en bloc and was placed on a 48 × 60 × 0.16 mm coverglass window in a specially designed Plexiglas chamber with ports for the tracheal, pulmonary, and left atrial cannulae. The cardiovascular ports were connected to a peristaltic pump that recirculated 40 ml of perfusate at a constant flow rate of 8 ml/min through the pulmonary vascular bed. The chamber was placed on the stage of an epifluorescence microscope fitted with a 60× objective (Nikon Diaphot TMD) and equipped with an optical filter changer (Lambda 10-2, Sutter Instrument Co., Novato, CA). A local anesthetic (0.05 mg of xylazine, Sigma) was injected subepicardially into the posterior wall of the right atrium to abolish lung movement artifact due to contraction of remaining cardiac muscle. Excitation of the lung surface was accomplished with a mercury lamp fiberoptic light source, a fluorescein isothiocyanate filter set for DAF-2T or Fluo-3 (HQ41001 with 480/40 excitation filter, 505 LP dichroic mirror, and 535/40 emission filter; a tetramethylrhodamine isothiocyanate filter set for DiI-acetylated LDL, Chroma Technology Corp., Brattleboro, VT). The integrity of the preparation was continuously monitored by online measurements of intratracheal and pulmonary artery perfusion pressures. Endothelial cells in the subpleural vasculature were positively identified by labeling with DiI-acetylated LDL added to the perfusate. We have used a Nikon Diaphot TMD epifluorescence microscope, a Hamamatsu ORCA-100 digital camera, and MetaMorph imaging software (Universal Imaging) for imaging. After an equilibration period of 45 min with the isolated lung to allow uptake of DAF-2 DA (5 µmol/liter), intravascular dye was removed by perfusion with dye-free medium for 5 min to reduce background fluorescence. Images of DAF-2T- or Fluo-3-stained vascular endothelial cells were taken from the same area as a stream (18 frames per s) or every 3 s for up to 10 min during which ventilation was stopped. As a control, after the equilibration period, images were taken during continuous perfusion. Then the peristaltic pump was stopped to create ischemia. Some lungs were pretreated with L-NAME (1 mmol/liter) by administration of perfusate during the dye equilibration period or with 1 µmol/liter thapsigargin. Additional lungs were perfused with calcium-free KRB containing 1 mmol/liter EGTA prior to ischemia.

Data Analysis-- For quantification, each endothelial cell was outlined and its fluorescence intensity was measured over time. For each lung, mean fluorescent intensities of 4-7 endothelial cells were averaged. Fluorescent intensity of 3-4 lungs for each condition was averaged. All results are expressed as mean ± S.E. for each condition. Comparisons were made using analysis of variance with Bonferroni's test using SigmaPlot 2000 (SPSS Inc.). Differences were considered to be significant at p < 0.05.

	RESULTS AND DISCUSSION

TOP ABSTRACT INTRODUCTION EXPERIMENTAL PROCEDURES RESULTS AND DISCUSSION REFERENCES

Endothelial cells in situ in subpleural microvessels of rat lungs exhibited progressive increase in DAF-2T fluorescence during ischemia indicating increased NO generation with abrupt cessation of shear stress compared with control perfusion (Fig. 1a). The fluorescent endothelial cells in subpleural precapillary arterioles could be readily identified as elongated, flow-aligned structures with tapered ends pointing against the flow direction and most of the fluorescence in the thicker part of the cells in the perinuclear area (Fig. 1a). Specific endothelial cellular identification was confirmed by colabeling with DiI-acetylated LDL that showed cellular colocalization with DAF-2T fluorescence (data not shown). Quantification of fluorescence intensity in the same endothelial cells over time and averaged for a few cells shows that the increase in DAF-2T fluorescence with ischemia was completely blocked by L-NAME (Fig. 2a), indicating specificity of the signal for NO.

View larger version (128K): [in this window] [in a new window]   Fig. 1.   a, effect of normoxic ischemia on DAF-2T fluorescence in subpleural endothelial cells in situ in the intact rat lung. DAF-2 DA was administrated in the perfusate for 45 min of equilibration, then images were acquired every 3 s for 10 min before and 10 min after ischemia (stopping of flow). Numbers in the images indicate time in min:s with start of ischemia as zero time. Only a few frames from one experiment that is representative of four separate experiments are shown. Endothelial cells are characterized by the elongated nuclear/perinuclear area shapes with the tapered ends pointing toward inflowing perfusate. Some frameshift is noticeable due to movement of the isolated lung preparation on the coverglass during imaging. During control perfusion at 8 ml/min (equivalent to ~33% of the resting cardiac output of the rat), DAF-2T fluorescence showed only a slight decrease in intensity probably reflecting some photobleaching due to multiple exposures. The increase in DAF-2T fluorescence with ischemia indicates increased NO generation that occurs as early as 1 min after ischemia. Images are in pseudocolor (intensity scale shown in panel b). b, effect of ischemia on Fluo-3 fluorescence in lung endothelial cells in situ. Fluo-3 was preperfused for 30 min prior to onset of ischemia. Imaging was done as described in panel a. The increase in Fluo-3 fluorescence in endothelial cells in situ indicates increase in intracellular Ca2+ with ischemia.

View larger version (54K): [in this window] [in a new window]   Fig. 2.   a, effect of NOS inhibition on DAF-2T fluorescence with ischemia. L-NAME pretreatment (Ischemia + L-NAME) completely blocked the increase in DAF-2T fluorescence with ischemia (Ischemia). Average pixel intensity of 4-7 endothelial cell areas as outlined using MetaMorph Imaging software was followed over time for each lung and expressed as percent change from initial fluorescence intensity. Each data point represents mean ± S.E. for 3-4 lungs. b, effect of inhibitors of calmodulin (calmidazolium chloride) and PI3-kinase (wortmannin) on DAF-2T fluorescence with ischemia. c, effect of ischemia and Ca2+-free perfusion on Fluo-3 fluorescence. Ca2+-free perfusion also included 1 mM EGTA. d, effect of depletion of intracellular Ca2+ stores on ischemic increase in Ca2+. Thapsigargin was administered in the perfusate 30 min before ischemia. For each lung, results for 4-7 endothelial cells were averaged; each data point represents the mean ± S.E. for 3-4 lungs for each condition.

Endothelial cells possess at least two isoforms of NOS: endothelial (eNOS) and inducible (iNOS) (14). eNOS requires increased levels of Ca²⁺ and calmodulin binding for its dissociation from caveolin and activation whereas activation of iNOS is Ca²⁺-independent (15). Ca²⁺-free medium containing 1 mM EGTA led a to marked decrease in DAF-2T fluorescence with ischemia (Fig. 2a), suggesting that eNOS is responsible for endothelial NO generation under these conditions. The calmodulin inhibitor, calmidazolium chloride, and the PI3-kinase inhibitor, wortmannin, markedly inhibited the ischemic increase in DAF-2T fluorescence (Fig. 2b). These results indicate a role for calmodulin binding and the protein kinase B/Akt-mediated phosphorylation for the activation of NOS in oxygenated ischemia. Dependence of NOS activation on both Ca²⁺ and PI3-kinase in pulmonary endothelial cells in situ with flow cessation contrasts with the dependence on PI3-kinase alone for sustained NOS activation associated with imposition of shear stress to cells in static culture (16). There was no evidence for a Ca²⁺-independent component as described previously for increased flow (10, 11, 17, 18).

To establish a temporal relationship between the NO and Ca²⁺ changes, we used Fluo-3 to monitor changes in endothelial cell Ca²⁺. Ischemia led to increased Ca²⁺ in endothelial cells in situ that was partially prevented by perfusion with either Ca²⁺-free, 1 mM EGTA-containing medium or by pretreatment with thapsigargin, an inhibitor of Ca²⁺-ATPase of endoplasmic reticulum (Fig. 1b and Fig. 2, c and d). These results indicated that ischemic increase in endothelial cell Ca²⁺ is due to both influx and intracellular release.

Comparison of the time course for the NO and Ca²⁺ responses to ischemia revealed that the onset of Ca²⁺ increase occurs between 10 and 20 s whereas the onset of NO increase is between 30 and 90 s for individual endothelial cells (Fig. 3a). Therefore, the ischemic increase in NO is preceded by an increase in Ca²⁺ in endothelial cells in situ. Along with the calmidazolium data (Fig. 2b), these results indicate that the temporal order of Ca²⁺ and NO increase with ischemia provides a stimulus and effect relationship between these phenomena.

View larger version (19K): [in this window] [in a new window]   Fig. 3.   a, temporal relationship between Ca2+ and NO changes with ischemia in pulmonary endothelial cells in situ. Changes in average pixel intensity from separate experiments are plotted as ischemia time of the same cell. Each data point represents mean ± S.E. of 4-7 endothelial cells for each of 4 lungs with DAF-2T or Fluo-3. b, schematic representation of the mechanotransduction hypothesis for response of endothelial cells in situ to ischemia. One or more primary flow sensors may be involved in the ischemic response. Voltage-dependent Ca2+ channels (VDCC) have been demonstrated in freshly isolated endothelial cells (19); Ca2+ increase during ischemia subsequent to cell membrane depolarization suggests their presence in endothelial cells in situ. The mechanism relating mechanotransduction (summarized as Ca2+-Releasing Factors) to Ca2+ release from intracellular stores with ischemia is not understood: a direct effect may involve force transmission via cytoskeleton, and an indirect effect may include Ca2+-induced Ca2+ release or other secondary pathways.

We have shown previously that ischemia in the normoxic lung leads to plasma membrane depolarization, increase in intracellular Ca²⁺, and reactive oxygen species generation and have hypothesized the involvement of a flow-sensitive K⁺ channel (6, 7, 9). This study shows that the increase in intracellular Ca²⁺ in endothelial cells with ischemia results in NO synthesis. We postulate that these ischemic responses are related to mechanotransduction of loss of shear stress, and a schema of this process is shown in Fig. 3b. Although depolarization-induced phenomena may depend on K⁺ channels and could trigger Ca²⁺ increase and the NO response, it is possible that another protein functions as the primary mechanosensor (20).

The study of the response of endothelial cells to mechanical stresses could theoretically utilize cells adapted to no-flow (e.g. in vitro under static culture) or cells that are flow-adapted. Most previous studies of the effect of shear stress examined responses of static cells upon exposure to flow; a few studies including the present one evaluated the responses of in situ flow-adapted cells to sudden loss of flow. Strikingly, some responses of the endothelial cells were shown to be identical in nature and direction for both types of stimuli, i.e. increased shear stress in nonadapted cells or loss of shear stress in adapted cells. These responses include pinocytosis (21), intracellular calcium (7, 22), and reactive oxygen species generation (8, 23). The present results show that the NO response of flow-adapted endothelial cells to loss of shear stress is similar in direction to the response following onset of flow for cells adapted to static conditions. Thus, the NO response represents another paradigm of alteration from a state of adaptation (24). For all of the shear stress-induced responses in the endothelial cell, the current notion of mechanotransduction requires the presence of sensors coupled to signal transduction pathways. Although the precise shear stress sensor is not known, it has been postulated that caveolae (cholesterol-rich microdomains of plasma membrane) may be involved in the NO response (25). Whether these represent a flow sensor remains to be determined. Further, it is not clear whether the same sensor responds to the onset as well as the loss of shear stress. In any event, adaptation of endothelial cells to flow or no flow may be determined primarily by the adaptation of flow sensors to mechanical shear, possibly with retention of similar signal transduction pathways and effectors under both conditions.

	ACKNOWLEDGEMENTS

We thank Maggie Meuler for excellent technical assistance, Dr. Harry Ischiropoulos for helpful discussions, and Dr. Yefim Manevich for suggesting the NO probe.

	FOOTNOTES

^* This work was supported by a Parker B. Francis fellowship (to A. B. A.) and National Institutes of Health, Specialized Center for Research in Acute Lung Injury Grant P50-HL60290 (to A. B. F.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Present address: 2nd Department of Surgery, Akita University School of Medicine, Akita, Japan.

^§ To whom correspondence should be addressed: Institute for Environmental Medicine, University of Pennsylvania Medical Center, One John Morgan Bldg., 3620 Hamilton Walk, Philadelphia, PA 19104-6068. Tel.: 215-898-9100; Fax: 215-898-0868; E-mail: abf@mail. med.upenn.edu.

Published, JBC Papers in Press, October 20, 2000, DOI 10.1074/jbc.C000702200

	ABBREVIATIONS

The abbreviations used are: NO, nitric oxide; NOS, nitric-oxide synthase; eNOS, endothelial NOS; iNOS, inducible NOS; DAF-2 DA, 4,5-diaminofluorescein diacetate; DAF-2T, diaminotriazolofluorescein; L-NAME, N^G-nitro-L-arginine methyl ester; LDL, low density lipoprotein.

	REFERENCES

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This Article Abstract Full Text (PDF) All Versions of this Article: 275/51/39807    most recent C000702200v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Al-Mehdi, A. B. Articles by Fisher, A. B. Search for Related Content PubMed PubMed Citation Articles by Al-Mehdi, A. B. Articles by Fisher, A. B. Social Bookmarking                      What's this?