| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
|
|
|
|||||||
|
|||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
,1
* Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA; and
Division of Pulmonary and Critical Care Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, Massachusetts, USA
1Correspondence: Division of Pulmonary and Critical Care Medicine, Brigham and Women’s Hospital, Harvard Medical School, 75 Francis St., Boston, MA 02115, USA. E-mail: amchoi{at}rics.bwh.harvard.edu
 |
ABSTRACT |
|---|
 TOP ABSTRACT INTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
Key Words: CNN • exocytosis • signaling
|
INTRODUCTION |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
2
3
4
5
6)
. The CCN proteins share a uniform modular structure and exhibit diverse cellular functions (1
2
3
4
5
6)
. Cyr61 (CCN1) mediates cell adhesion, migration, proliferation, cell survival, apoptosis, and angiogenesis (3
, 6
, 7
8
9)
. It is a secreted heparin-binding protein that integrates into the extracellular matrix (ECM) (9
10
11
12
13)
. Cyr61 as secreted protein is internalized and degraded through the lysosomal pathway (14)
and functions as an autocrine or paracrine protein through integrins (9
10
11
12
13)
. It can either induce or suppress apoptosis in a cell type-dependent manner. While Cyr61 promotes survival of endothelial cells, myocytes, and breast cancer cells (9
, 13
14
15
16
17)
, its expression was associated with cell death in neuronal cells (18)
.
Our previous studies showed that Cyr61 protected hyperoxia-induced lung cell death via Akt phosphorylation (19)
. However, whether and how Cyr61 interacts with integrins and subsequently induces phosphorylation of Akt in lung cells remains unclear. In this study, we identified a novel component, caveolin-1, involved in Cyr61 signaling.
The domain structure characterized by lipid packing in the lipid bilayer of plasma membrane consists of cholesterol, sphingolipids, and certain proteins. These regions are defined as cholesterol-enriched membrane microdomains (CEMMs), also known as "lipid rafts" (20)
. Caveolae are one subset of lipid rafts that are distinct cholesterol- and sphingomyelin-rich, omega-shaped invaginations (50–100 nm) of the plasma membrane (21)
. These structures are dynamically recycled in the plasma membrane, endosomes, and trans-Golgi systems, and participate in a number of cellular processes, including endocytosis, transcytosis, and intracellular signal transduction (20
21
22
23
24
25)
. Caveolin-1 (cav-1), a 22-kDa transmembrane scaffolding protein, serves as the principle structural component of caveolae (20
21
22
23
24
25)
. Accumulating data indicate that cav-1 regulates signal transduction-associated proteins that reside in the caveolae. Direct inhibition by cav-1 has been reported on many proteins, such as Src, the epidermal growth factor (EGF) receptor, endothelial nitric-oxide synthase (eNOS), G protein 
and subunits, and H-Ras, (26
27)
. Direct activation by cav-1 on insulin receptors has also been found (25)
. Moreover, numerous integrin-mediated pathways are dependent on caveolin-1, including ERK, PI3K/Akt, and Rac pathways (29
, 30)
. Integrins regulate cellular processes by controlling the localization of caveolae at the plasma membrane. Loss of integrin-mediated adhesion results in the internalization of caveolae which, in turn, terminates signaling pathways, including activation of multiple integrin-mediated signaling (28
29
30
31
32)
. So far, we know that three integrin-dependent pathways (PI3K/Akt, Ras/ERK, and Rac/Pak) for cell proliferation and survival are impaired by caveolae internalization (26
27
28
29
30
31
32)
. Integrins prevent down-regulation of ERK, PI3K/Akt, and Rac-dependent pathways by inhibiting cav-1-mediated endocytosis (26
27
28
29
30
31
32)
.
Cyr61 is well known to function via integrin-mediated pathways (1
, 4
, 5)
. However, to our best knowledge, there is no report whether caveolin-1 is involved in Cyr61-mediated signaling pathways. Our study, demonstrates that cav-1 is involved in Cyr61-integrin signaling and mediated the protective role of Cyr61 in hyperoxia-induced lung cell and tissue injury.
|
MATERIALS AND METHODS |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
Cell culture and treatments
Primary mouse lung fibroblasts and pulmonary endothelial cells were cultured as described previously (33)
and used for experiments as subconfluent monolayers at passages 7–12. Cells were cultured from the lungs of wild-type C57BL/6 mice and caveolin-1-null (cav-1–/–) mice, as described previously (33)
. Beas-2B lung epithelial cells were purchased from American Type Culture Collection (Manassas, VA, USA) and cultured in the defined medium, BEGM (bronchial epithelial growth medium; Cambrex, East Rutherford, NJ). All cells were grown in humidified incubators containing an atmosphere of 5% CO2 and 95% air at 37°C. Cell cultures were exposed to hyperoxia in modular exposure chambers as described (19)
, using 95% oxygen with 5% CO2.
Animal exposures
Wild-type C57BL/6 mice and inbred cav-1–/– mice, 8–12 wk, were maintained in laminar flow cages in a pathogen-free facility at the University of Pittsburgh. All procedures were performed in accordance with the Council on Animal Care at the University of Pittsburgh and the National Research Council’s Guide for the Humane Care and Use of Laboratory animals. The cav-1–/– mice were purchased from Jackson Laboratories (Bar Harbor, ME, USA). The animals were exposed to room air or hyperoxia (95% O2, 5% N2). Mice underwent bronchial-alveolar lavage (BAL) and then were sacrificed at 96 h exposure.
Transfections
Beas-2B cells were transfected with cav-1 siRNA using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA). Transiently transfected cells were incubated for an additional 24 h and exposed to hyperoxia. After 48–72 h, cell viability was determined with cell viability assay (Promega, Madison, WI, USA). The rest of the cells were harvested for the determination of caveolin-1 expression. Small-interfering RNA (siRNA) was designed against the coding sequence of caveolin-1 cDNA by using software by Dharmacon Research (Layfayette, CO, USA). Sequences corresponding to the siRNAs were as follows: human caveolin-1 coding region, (CCAGAAGGGACACACAGTT), GenBank accession no. NM_001753.
Immunoprecipitation, Western blot analysis, and immunocytochemistry
After 16–24 h hyperoxia, proteins were isolated from cell cultures in radioimmunoprecipitation assay buffer [1x PBS, 1% (v/v) Nonidet P-40, 0.5% (w/v) sodium deoxycholate, 0.1% (w/v) sodium dodecyl sulfate, 0.1 mg/ml phenylmethylsulfonyl fluoride, 30 µl/ml aprotinin, and 1 mM sodium orthovanadate]. Protein concentration was determined using the Coomassie plus protein assays (Pierce, Rockford, IL, USA) and was equalized between samples. For immunoprecipitation, 1 µg of antibody was added to 500 µg of total protein in 500 µl, rotated overnight at 4°C, and then incubated with 20–30 µl of beads (protein A–sucrose; Santa Cruz Biotechnology) for 2–4 h, spun down at 500 g, and washed 3 times with radioimmunoprecipitation buffer. Then, 30 µl of loading buffer (100 mM Tris-HCl, 200 mM dithiothreitol, 4% SDS, 0.2% bromphenol blue, and 20% glycerol) was added. For SDS-PAGE, samples containing equal amounts of protein were boiled in the loading buffer and separated on SDS-PAGE, followed by transfer to polyvinylidene difluoride membranes. The membranes were blocked with 5% nonfat milk and stained with the primary antibodies for 2 to 12 h at 1:250 to 1:1000 dilution. After 5 washes in phosphate-buffered saline with 0.2% Tween 20, the horseradish peroxidase-conjugated secondary antibody was applied, and the blot was developed with enhanced chemiluminescence reagents (Amersham Biosciences, Piscataway, NJ, USA).The following antibodies were used for immunoblotting: monoclonal anticav-1, (BD Transduction Laboratories), polyclonal anticav-1 (Santa Cruz Biotechnology), polyclonal rabbit and goat anti-Cyr61 (Santa Cruz). Immunocytochemistry was performed as described previously by the Center for Biological Imaging at the University of Pittsburgh (33)
.
Quantitative reverse transcriptase-polymerase chain reaction (RT-PCR)
RNA was extracted from cells using TRIzol method (Invitrogen) and was converted to cDNA using a high-capacity cDNA archive kit (Applied Biosystems, Foster City, CA, USA). Quantitative RT-PCR analyses were performed as described previously (34)
; probes and primers for Cyr61 and TaqMan Master Mix for gene expression assays were obtained from Applied Biosystems. Gene expression was analyzed by the 
Ct method, with 18s rRNA and βGUS as the endogenous control.
Cell viability assay
Cell viability assays were performed using the CellTiter-Glo Luminescent Cell Viability Assay according to the manufacturer’s protocol (Promega). Briefly, cells were plated into 96-well plates. After transfection and exposure to hyperoxia, cells were washed twice with cold PBS. One hundred microliters of PBS was added into each well, followed by 100 µl CellTiter-Glo Substrate. Cells were incubated at room temperature for at least 10 min; luminescent signal was then measured using an Lmax luminometer (Molecular Devices, Sunnyvale, CA, USA).
Statistical analysis
All values are expressed as means ± SD from at least three independent experiments. Differences in measured variables between experimental and control group were assessed by using the Student’s t test (Statview II statistical package; Abacus Concepts, Berkeley, CA, USA). Statistically significant difference was accepted at P < 0.05.
|
RESULTS |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
. In the current study, recombinant Cyr61 with biological activity was used to treat Beas-2B cells and primary fibroblasts. A dose-dependent effect was observed on cell proliferation, both on epithelial cells (Fig. 1A
) and fibroblasts (data not shown). Then we evaluated the effect of recombinant Cyr61 on cell survival after hyperoxia (72 h). Besides its effect on cell proliferation, Cyr61 conferred increased resistance to hyperoxia-induced cell death in a dose-dependent manner (Fig. 1B
). Trypan blue exclusion assays were performed to confirm the observation in Fig. 1B
, indicating that the resistance to hyperoxia-induced cell death was independent of cell proliferation (data not shown).
|
Cyr61-neutralizing antibodies reversed the protective effects
Coating plates with Cyr61-neutralizing antibodies and control immunoglobulin G (IgG), we investigated the cell survival after hyperoxia (72 h) using Beas2B and fibroblasts. After hyperoxia (72 h), cell survival in the neutralizing antibody group was significantly less than that in the control IgG group. These results were similar in both Beas-2B cells and fibroblasts (Fig. 2A
and data not shown).
|
Besides Beas2B and wild-type fibroblasts, we further investigated the response to hyperoxia-induced cell death in cav-1–/– fibroblasts. Cav-1–/– fibroblasts were more resistant to hyperoxia than wild-type fibroblasts (Fig. 2B
). Interestingly, Cyr61-neutralizing antibodies attenuated the protective effect of cav-1 deletion (Fig. 2B
).
Colocalization and interaction between Cyr61 and cav-1
The above findings prompted us to evaluate the crosstalk between cav-1 and Cyr61. First, we used confocal microscopy to test whether Cyr61 and cav-1 colocalized. We found that Cyr61 and cav-1 colocalized at the surface of the cell membrane in room air (Fig. 3A
). This colocalization of Cyr61 and cav-1 at the surface attenuated after hyperoxia (data not shown). Furthermore, we confirmed the colocalization between Cyr61 and cav-1 by performing coimmunoprecipitation (co-IP) experiments. Strong interactions between Cyr61 and cav-1 were found in cells in room air. Interestingly, hyperoxia exposure decreased these interactions (Fig. 3B
). To further validate our results, we determined the level of cell death in the same conditions under which IP/confocal microscopy was performed. Twenty-four hours after hyperoxia, 80% of Beas2B cells remained alive, and the expression of cav-1 in these viable cells was not altered by hyperoxia (data not shown). Given that we equalized the amount of protein used for co-IP, the attenuated band between cav-1 and Cyr61 after hyperoxia was due to dissociation of this complex.
|
Cyr61 and cav-1 colocalization was mediated via integrins
Given that the cav-1-binding motif is not present in Cyr61, we further evaluated whether these two proteins interacted via integrins. We performed co-IP experiments on Cyr61 or cav-1 with integrin V subunits or integrin β3 subunits, respectively. As shown in Fig. 4
, Cyr61 or cav-1 coimmunoprecipitated with integrin V and integrin β3 subunits. While hyperoxia decreased the interactions between Cyr61 and either integrin V or integrin β3 subunits, it had no significant effect on cav-1/integrins (Fig. 4
).
|
Integrin V mediates Cyr61/Cav-1 interaction
To further confirm the critical role of integrins in Cyr61 and cav-1 interaction, we transfected integrin V siRNA into Beas2B cells. After 24 h of hyperoxia, total cell lysates were collected, immunoprecipitated with polyclonal Cyr61 antibody, and blotted with monoclonal cav-1 antibodies. The same blot was then stripped to check for Cy61 pulldown. The interaction between Cyr61 and cav-1 decreased with hyperoxia, as well as after treatment with integrin V siRNA (Fig. 4C
). To confirm that this observation was not due to the significant cell death caused by integrin siRNA, we transfected cells with integrin V siRNA. Cells were then evaluated for viability; counts are shown in Fig. 4D
. We found that integrin V siRNA had no significant effect on cell death with or without hyperoxia, compared with the control siRNA in our model.
Cav-1 expression regulates intracellular level of Cyr61
Given that cav-1 and Cyr61 colocalized to the cell surface (Fig. 3
), we questioned whether cav-1 mediates the secretion of Cyr61. We tested the intracellular level of Cyr61 in both wild-type and cav-1–/– cells. Cyr61 protein levels significantly decreased in cav-1–/– cells compared with wild type (Fig. 5A
). To verify this observation in Beas2B epithelial cells, we performed knockdown assays using cav-1 siRNA. We observed similar effects as in fibroblasts, with decreased Cyr61 levels in cav-1 siRNA-treated Beas2B epithelial cells (Fig. 5B
). We further confirmed this result with knock-in assays. Using adeno-cav-1, we overexpressed cav-1 in cav-1–/– cells. With increased levels of cav-1, we observed increased amounts of intracellular Cyr61 (Fig. 5C
).
|
Deletion of cav-1 (cav-1–/–) increased extracellular level of Cyr61 in vitro and increased the secreted Cyr61 in vivo
Next, we evaluated the extracellular level of Cyr61 in the absence of cav-1 using cav-1–/– cells. Supernatants of cell culture media from wild-type cells and cav-1–/– cells were collected and precipitated with trichloroacetic acid (TCA). Then, using Western blot analysis, we compared the secreted Cyr61 of wild-type cells and cav-1–/– cells with and without hyperoxia. Supernatant from culture medium of cav-1–/– cells exhibited increased Cyr61 protein (Fig. 6A
) compared to wild-type control cells. Furthermore, we exposed cav-1–/– mice to room air and hyperoxia. After 72 h, we performed whole lung lavage. BAL fluid was collected, and protein was precipitated using TCA. We found more Cyr61 in the BAL fluid of cav-1–/– mice than of wild-type mice (Fig. 6B
).
|
Hyperoxia exerted no effect on cav-1 expression
Since the amount of caveolae/cav-1 potentially affects the level of Cyr61, we next questioned whether hyperoxia induces cav-1 expression. Using Beas-2B cells, endothelial cells, wild-type fibroblasts, and cav-1–/– fibroblasts, we did not observe significant changes of cav-1 expression (Fig. 5A-C
, left columns, and data not shown). Furthermore, we performed Western blot analysis and did not find any difference in cav-1 levels between wild-type mice and cav-1–/– mice (Fig. 6B
).
Exocytosis of Cyr61 was enhanced in cav-1–/– cells
To test whether the lack of intracellular Cyr61 was due to enhanced exocytosis of Cyr61, we treated the cav-1–/– fibroblasts with Brefeldin A (BFA), a metabolite of the fungus Eupenicillium brefeldianum, which has a disruptive effect on the putative ER and Golgi vesicular network. Intracellular Cyr61 was significantly higher in BFA-treated cells regardless of treatment (Fig. 7A, B
). On the contrary, secreted Cyr61 was less in the supernatant of cell culture medium (Fig. 7B
), which was prominent in the absence of cav-1.
|
Hyperoxia increased Cyr61 gene expression
One of the remaining questions would be whether hyperoxia modulated Cyr61 gene expression. As shown in Fig. 8A
, hyperoxia induced Cyr61 expression after 24 h hyperoxia in Beas-2B cells. This result is consistent with our previous findings (19)
. We then performed Taqman assays to evaluate the Cyr61 gene expression after hyperoxia. As shown in Fig. 8B
, hyperoxia increased Cyr61 mRNA 
3- to 4-fold comparing with the room air (Fig. 8B
).
|
|
DISCUSSION |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
, 9
, 10
, 13
14
15
, 17
, 18)
. In our previous study, we found that Cyr61 played a protective role in hyperoxia-induced cell death via Akt-related pathways (19)
. Cyr61, as the secreted protein, is internalized and degraded through the lysosomal pathway (14)
. It can function via an autocrine or paracrine effect (5
6
7
8
9
10
11)
. Integrins act as its receptors and regulate its downstream signaling (3
4
5
6
7
8)
. Caveolae, as a subset of lipid rafts, can recruit and exclude signaling proteins (20
21
22
23
24
25)
. The close contact of receptors and signaling proteins in caveolae facilitates efficient signal transduction. It has been shown that caveolin-1, the major component of caveolae, is involved in integrin signaling (23
24)
.
Many reports have indicated a countereffect on cell survival and proliferation between integrins and caveolin-1. Integrins negatively regulate caveolae internalization, preventing uncoupling of signaling molecules, such as Rac disengagement from its effector, Pak (23
24)
. Similar mechanisms apply to other pathways, such as ERK and PI3K/Akt. At least three integrin-dependent growth pathways (Ras/ERK, PI3K/Akt, and Rac/Pak) are impaired by Cav-1-mediated caveolae internalization (25
26
27
28
29
30
31
32)
. Cav-1 links integrin signaling to growth-limit pathways; deletion of cav-1 will dissociate integrins from growth-regulatory pathways and result in tumor-like, anchorage-independent growth (25
26
27
28
29
30
31
32)
(Fig. 9
).
|
Previous studies indicated Cyr61 promotes chemotaxis, proliferation, migration, and intravasation via integrins/Src/PI3K/Akt-dependent pathways (1
, 4
, 13
, 15
16
17
18
19)
. Although integrins are involved in both Cyr61 and Cav-1 on different occasions, to the best of our knowledge, Cyr61 and cav-1 colocalization and interaction have not been studied. Also, whether cav-1 and caveolae play a role in Cyr61 signaling remains unexplored.
Here, we report for the first time that Cyr61 can signal through caveolae in connection with integrin-mediated pathways. Moreover, our studies showed that cav-1/Cyr61 interaction played a role in regulating Cyr61 exocytosis. Secretion of Cyr61 was enhanced in cav-1–/– cells (Figs. 5
6
7
and 9
). Treatment with BFA, a metabolite of fungus that disrupts Golgi apparatus and protein exocytosis, elevated the intracellular level of Cyr61 in cav-1–/– cells. Without disruption of exocytosis, naturally elevated extracellular Cyr61 in cav-1–/– cells indicated an augmented autocrine/paracrine effect by secreted Cyr61 in matrix (Figs. 7
and 9
). In our model, cav-1–/– cells had more rapid proliferation and higher resistance to hyperoxia. This result supports our hypothesis. The elevated secretion of Cyr61 from cav-1–/– cells stimulates cell proliferation and protects cells from hyperoxic cell death via integrin-mediated pathways. The protective effect of Cyr61 after hyperoxia was not counterbalanced by cav-1 in this case. In other words, without cav-1, cav-1–/– cells increased Cyr61 secretion (Fig. 7
). Extracellular Cyr61 and its persistent engagement with integrin complexes (in our case, integrin Vβ3) will result in cell survival and uncontrolled proliferation, probably via a PI3K/Akt–dependent pathway (Fig. 9
). Indeed, in our previous work, knocking down phosphor–Akt significantly reversed the protective effects of Cyr61 in hyperoxia-induced cell death (19)
. Interestingly, studies from the other groups also showed that the absence of cav-1 and caveolae results in activation of an integrin-dependent PI3K/Akt pathway (25
26
27
28
29
30
31
32)
, which is consistent with our results. Whether this is due to the effect of Cyr61 requires further investigation.
As expected, blocking the circulating Cyr61 in extracellular matrix by Cyr61-neutralizing antibodies attenuated the proliferation and protective effects of cav-1–/– (Fig. 5
). Therefore, we suspect that the increased proliferation and resistance to hyperoxia-induced cell death in cav-1–/– cells were due to the following factors. 1) Absence of cav-1 resulted in increased secretion of Cyr61. Given its autocrine and paracrine features, elevated Cyr61 in matrix will lead to increased cell proliferation and decreased cell death after hyperoxia in our model. 2) The deletion of caveolin-1 from integrin /cyr61 complex may result in decreased integrin/Cyr61 internalization, subsequently leading to unbalanced Cyr61 signaling and leading to proliferation/resistance to cell death. This is possibly mediated via a PI3K/Akt-dependent pathway. However, our current study did not focus on the internalization of Cyr61-integrin complex. Whether cav-1 affects the internalization of this complex requires further study. Previous reports had demonstrated that CCN1/Cyr61 inhibited apoptosis and induced proliferations via Akt pathways (13
, 15
16
17
18
19)
. Cyr61 has been shown to stimulate two common cell survival pathways, including PI3K/Akt and ERK1/2 mitogen-activated protein kinase (MAPK) (13
, 15
16
17
18
19)
. Recent data show that these pathways are integrin mediated (1
, 4
, 13
, 15
16
17
18
19)
. Yoshida et al. (15)
had demonstrated that in cardiac myocytes, β1 integrin mediated the phosphorylation of Akt by Cyr61-promoted cardiac myocyte survival under oxidative stress. Our data here provide a novel mechanism of Cyr61’s effect on proliferations and its protective role in apoptosis. Cav-1 induced cell death via an integrin-mediated pathway. Deletion of cav-1 in the Cyr61/integrin complex promoted cell proliferation and prevented cell death under stress, such as hyperoxia.
While it increased the gene expression of Cyr61 (Fig. 8
), hyperoxia decreased the interactions of Cyr61 and cav-1, as well as integrins (Figs. 3
and 4
). Hyperoxia had no significant effects on cav-1/integrin complex (Fig. 4
). This result indicated that Cyr61 may have a potential countereffect of cav-1. After stress, such as hyperoxia, the Cyr61/integrin complexes were dissociated, leading to less survival signaling via Akt pathways. On the other hand, cav-1 remained to bind with integrins and terminated survival signaling, further limiting the survival signaling or promoting death signaling. The decreased interactions between Cyr61 and cav-1 might be secondary to the lack of interactions of Cyr61/integrins, given that integrins act as a "bridge" between Cyr61 and cav-1. Cells responded to the hyperoxia-induced Cyr61 dissociation from Cyr61/integin complex by increased endogenous expression of Cyr61, as reported in our previous work (19)
. We further evaluated the potential involvement of mTOR pathway in our studies, given that hyperoxia is well known as a potent translation inhibitor through inhibition of the mTOR pathway. Hyperoxia down-regulated the phosphor-p70 S6 kinase (data not shown). However, between wild-type and cav-1–/– cells, there is no significant difference on p-P70 S6K after hyperoxia (data not shown).
A few questions arose from this work. We have shown that deletion of cav-1 enhanced the secretion of Cyr61, whereas overexpressing cav-1 increased the intracellular level of Cyr61 (Fig. 5
). Whether cav-1 has both an effect on decreasing Cyr61 secretion and enhancing Cyr61/integrin internalization remains unclear. Furthermore, whether Cyr61 prevents cav-1-mediated internalization or only limits the cav-1/integrin signaling by competitive inhibition requires further investigation. We have performed co-IP between cav-1 and Cyr61 in the cytoplasm fraction. However, there is no interaction. Indeed, there is a negligible level of cav-1 in the cytoplasm fraction (data not shown). Previous studies have suggested that Cyr61 secretion utilizes an ER-Golgi apparatus (35)
, but the internalization after secretion may use endocytosis-lysosomal degradation routes (14)
. So the Cyr61 transport from synthesis probably uses the same routes as cav-1 (ER-Golgi), which may explain the cytoplasm colocalization of cyr61 and cav-1. This hypothesis will be one of our future focuses.
Moreover, the mechanisms by which cav-1, integrin vβ3, and Cyr61 interact to inhibit exocytosis of Cyr61 remain unclear. Cyr61 comprises four major modules, one of which is a cysteine knot, heparin-binding domain (module IV) (36)
. Stress, including hyperoxia, presumably oxidizes these cysteine domains and subsequently changes the conformation of the Cyr61 molecule. Cav-1 is a palmitoylated protein involved in assembly of signaling molecules in caveolae and in intracellular cholesterol transport. Protein palmitoylation is a post-translational modification and is reversible. Three cysteine residues in the C terminus of caveolin-1 are subject to palmitoylation (37
, 38)
. The palmitoylation of the cysteine residue of cav-1 may be regulated by stress, such as hyperoxia, which, in turn, may regulate the conformation, membrane association, protein-protein interactions, and intracellular localization of the cav-1. However, further investigation is required to confirm this hypothesis.
After hyperoxia, expression of integrins and cav-1 did not change in whole-cell extracts, as shown in Fig. 5
. In viable cells, hyperoxia did not alter the amount of cav-1 in membrane-bound protein, as indicated by cell fractionation analyses (data not shown).
Last, another potential focus of our future studies will be evaluation of whether other integrins, such as 6β1, are involved in Cyr61/integrin/cav-1 complex signaling.
In summary, our data for the first time showed that cav-1 is involved in Cyr61/integrin signaling during cell proliferation and cell survival after hyperoxia. Its effect might be mediated by interaction with integrins.
|
ACKNOWLEDGMENTS |
|---|
Received for publication April 23, 2008. Accepted for publication August 29, 2008.
|
REFERENCES |
|---|
|
TOPABSTRACTINTRODUCTIONMATERIALS AND METHODSRESULTSDISCUSSIONREFERENCES |
|---|
, B. V., Kolesnikova, T. V., Chen, C. C., Yang, G. P., Abler, A. S., Lau, L. F. (1997) Cyr61 and Fisp12 are both ECM-associated signaling molecules: activities, metabolism, and localization during development. Exp. Cell. Res. 233,63-77[CrossRef][Medline]This article has been cited by other articles:
|
|
 |
|
  M. Zhang, L. Lin, S.-J. Lee, L. Mo, J. Cao, E. Ifedigbo, and Y. Jin Deletion of caveolin-1 protects hyperoxia-induced apoptosis via survivin-mediated pathways Am J Physiol Lung Cell Mol Physiol, November 1, 2009; 297(5): L945 - L953. [Abstract] [Full Text] [PDF]
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
