Assessment of endothelium and inflammatory response at the onset of reperfusion injury in hand surgery
© Kamat et al.; licensee BioMed Central Ltd. 2012
Received: 4 October 2011
Accepted: 14 May 2012
Published: 14 May 2012
Activation of the endothelium, complement activation and generation of cytokines are known events during ischemia-reperfusion (I/R) that mediate tissue injury. Our aim was to elucidate their respective participation at the onset of the reperfusion phase. Tourniquet application in hand surgery causes short-term ischemia, followed by reperfusion and was therefore used as the model in this study.
Ten patients were included in the study after obtaining informed consent. A tourniquet was placed on the upper arm and inflated to 250 mmHg for 116 ± 16 min, during which the surgery was performed. Venous blood and tissue samples from the surgical area were taken at baseline as well as 0, 2, and 10 min after reperfusion and analyzed for the following parameters: Endothelial integrity and/or activation were analyzed by measuring heparan sulfate and syndecan-1 in serum, and vWF, heparan sulfate proteoglycan as well as CD31on tissue. Complement activation was determined by C3a and C4d levels in plasma, levels of C1-inhibitor in serum, and IgG, IgM, C3b/c, and C4b/c deposition on tissue. Cytokines and growth factors IL-5, IL-6, IL-7, IL-8, IL-10, IL-17, G-CSF, GM-CSF, MCP-1, TNFα, VEGF, and PDGF bb were measured in the serum. Finally, CK-MM levels were determined in plasma as a measure for muscle necrosis.
Markers for endothelial activation and/or integrity as well as complement activation showed no significant changes until 10 min reperfusion. Among the measured cytokines, IL-6, IL-7, IL-17, TNFα, GM-CSF, VEGF, and PDGF bb were significantly increased at 10 min reperfusion with respect to baseline. CK-MM showed a rise from baseline at the onset of reperfusion (p < 0.001) and dropped again at 2 min (p < 0.01) reperfusion, suggesting ischemic muscle damage.
In this clinical model of I/R injury no damage to the endothelium, antibody deposition or complement activation were observed during early reperfusion. However, an increase of pro-inflammatory cytokines and growth factors was shown, suggesting a contribution of these molecules in the early stages of I/R injury.
KeywordsTourniquet Hand surgery Ischemia Reperfusion injury Cytokines Complement Endothelium Glycocalyx
Ischemia / reperfusion (I/R) injury is a common source of pathology in many vascular diseases. Mechanisms underlying I/R injury have been studied extensively and are known to engage a spectrum of pathways. Elucidating the key molecules involved in triggering the entire process of injury is important to help develop targeted therapy to attenuate I/R injury in its early stages.
In any vascularized organ or tissue, a monolayer of endothelial cells (EC) forms the interface between blood and the surrounding tissue. Among other factors, the glycocalyx covering the endothelium, plays a critical role in maintaining the homeostasis of the blood vessel wall . The conditions during I/R cause this glycocalyx layer to partly shed , which occurs already during ischemia and more significantly during reperfusion . Glycocalyx shedding activates the endothelium by transforming it into a pro-inflammatory and pro-coagulant phenotype , thereby propagating injury. Moreover, the glycocalyx acts as an interface between blood and tissue, forms receptors for many inflammatory molecules including cytokines and therefore participates in inflammation [5, 6]. Shedding of the glycocalyx after 2 min of reperfusion has been shown in humans , but the respective study was based on a setting of cardiopulmonary bypass and data on I/R induced shedding of the glycocalyx in smaller, peripheral blood vessels are lacking.
Complement activation leads directly to tissue necrosis and trafficking of immune cells. Various knockout animal models have illustrated the participation of natural antibodies and complement in propagation of I/R injury [8, 9]. The importance of complement in I/R injury has been reviewed . Complement thus has the potential to significantly contribute to early reperfusion injury.
The model used in this study was that of tourniquet-induced I/R injury. Tourniquet application in extremity surgery is a prerequisite to provide a blood-less environment during surgery. The blood flow in the ischemic limb is restored after surgery by releasing the tourniquet. Use of the tourniquet thereby comes with the risk of I/R injury. Clinically, this manifests as pain, swelling, prolonged hypoesthesia of peripheral nerves, tissue necrosis along with systemic effects, which the surgeons try to avoid by limiting tourniquet times to a maximum of 2 hours [11–15]. Several studies in humans have been dedicated to understanding I/R injury due to tourniquet application in upper and lower limbs. These studies have shown the involvement of radical oxygen species (ROS) , expression of adhesion molecules , recruitment of activated leukocytes  and thereby progression of inflammation. The process of I/R injury in skeletal muscle has been extensively studied  and reviewed . However, the role of cytokines during early reperfusion is still unclear and yet to be investigated in upper limb I/R injury. This would be important, as cytokines apart from trafficking immune cells are known to cause shedding of the endothelial glycocalyx .
Based on the above-cited literature, including our own studies, we hypothesized that the endothelium together with the innate immune response including natural antibodies, complement, cytokines and growth factors, would be involved in the very early reperfusion phase. The aim of this study was to assess the involvement and relative contribution of these different factors in the initial phase of reperfusion injury.
Main disease for operation
Location of operation
Statins or Aspirin
Tourniquet time (min)
Tendon adhesions after complex reconstruction of left hand
Flexor tendon rupture left hand
Tendon adhesions after complex reconstruction of right hand
Ulnar nerve compression left elbow
Ulnar nerve compression left elbow
Rhizarthrosis right hand
Posttraumatic arthritis of distal radio ulnar joint of left hand
Lamotrigine, Amitriptyline Sodium valproate, Carvedilol, Chlorthalidone, Captopril / Hydrochlorothiazide
Rhizarthrosis right hand
Scaphoid non union right hand
Rhizarthrosis right hand
Hypertension, 16 years prior PTCA and stent
Atenolol, Ranitidine, Levothyroxine (0.1 mg), Estradiol (1 mg)
The tourniquet device was the A.T.S. 2000 automatic Tourniquet System (Zimmer, Inc. Warsaw, IL, USA) with a low profile cuff and accurate pressure monitoring. Before the cuff was applied on the upper arm a cuff sleeve to reduce shearing of soft tissue was used. After standardized disinfection with 0.5% chlorhexidin and sterile dressing surgery, samples were collected for the study.
Venous blood leaving the surgical area was collected from the cubital vein, distal to the tourniquet, with a sterile syringe. Collected blood was immediately transferred into S-monovette tubes (Sarstedt AG, Nümbrecht, Germany) containing EDTA (1.6 mg/ml) to obtain EDTA-plasma, and to tubes containing a clotting activator (glass pearls) to obtain serum. Samples were collected before application of tourniquet (baseline), and immediately after release of the tourniquet (at 0, 2 and 10 min after reperfusion). Samples were kept on ice until centrifugation at 3000 rpm for 10 min. Serum and EDTA-plasma were stored in aliquots at −80°C until use.
Subcutaneous tissue samples containing blood vessels were taken from the surgical area distal to the tourniquet, and therefore within the ischemic area. Sampling was done immediately after the application of tourniquet (baseline), just before releasing the tourniquet (end ischemia) and 10 minutes after release of tourniquet (10 min reperfusion). Biopsies were fixed in 2% formaldehyde for 24 hours and then transferred into 18% sucrose for 15 hours. They were embedded in Shandon M1 embedding matrix (Thermo Scientific, Inc., Geneva, Switzerland) and stored at -20°C until sectioned.
Markers for EC integrity/activation and detection of complement activation on tissue
Free float technique was used for immunostaining of tissue samples. In brief, 30 μm thick cryosections were cut from each sample and treated with TBS-Triton X100 for 15 min. EC integrity/activation were assessed by mouse anti-human heparan sulfate proteoglycan (HSPG; Abcam plc., Cambridge, UK), mouse anti-human von Willebrand factor (vWF; DAKO, Glostrup, Denmark), mouse anti-human CD31 (eBioscience, Inc., San Diego, CA, USA). As secondary antibodies we used Dylight 488 labeled donkey anti-mouse (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA, USA), Cy3-labeled donkey anti-mouse (Jackson ImmunoResearch) and FITC labeled rabbit anti-mouse (DAKO).
The following antibodies were used to determine natural antibody binding and complement activation: Cy3 labeled goat anti-human IgG (KPL, Inc., Gaithersburg, MD, USA), allophycocyanin labeled goat anti-human IgM (Open Biosystems / Thermo Scientific), FITC labeled rabbit anti-human C3b/c (DAKO), and FITC-labeled rabbit anti-human C4b/c (DAKO).
Scoring of stained tissue sections
The sections had highly heterogeneous vessel sizes approximately ranging between 12 – 100 μm. The variation due to vessel size and inter-batch differences during the staining procedure were overcome by the following scoring protocol: Sections of skeletal muscle from the hand of a healthy human were used as common control in every staining batch. Images of a representative blood vessel were taken under the confocal microscope from all sections including the common control. With Imaris software (Bitplane AG, Zurich, Switzerland), the area of the vessel was calculated from the image, and a histogram of the color channel of interest for the same area was obtained. The histogram of the common control was used to normalize histograms of other tissues from the same batch. This enabled sections from different batches to be comparable. Area under the curve (AUC) values were obtained from the normalized histogram for each tissue and divided by the area of the vessel to obtain a final score for the section. Sections were then compared with their final scores, which considered the size of the vessel and the intensity of staining within that vessel. Sections were blinded at all times for the analysis.
Analysis of EC integrity/activation and complement activation in venous blood
ELISA kits were used to determine the concentrations of heparan sulfate (HS) and syndecan-1 as markers of EC activation. Kits for C3a, C4d and functional C1-inhibitor were used to analyze complement activation. Assays were performed according to manufacturers' protocols and concentrations were determined by comparing with standards provided with the kit. HS (Seikagaku Corp., Tokyo, Japan) and syndecan-1 (Diaclone, Gene-Probe Inc., San Diego, CA, USA) were measured in blood serum samples. C3a and C4d (Quidel Corp., San Diego, CA, USA) were measured in EDTA plasma samples and functional C1-inhibitor (Quidel Corp., San Diego, CA, USA) measured in blood serum.
Analysis of cytokines in circulation
A multiplex immunoassay, consisting of fluorescent microspheres conjugated with a monoclonal antibody specific for a target protein, was used to detect an array of cytokines. Kits for IL-5, IL-6, IL-7, IL-8, IL-10, IL-17, G-CSF, GM-CSF, MCP-1, TNFα, VEGF, and PDGF bb were purchased from Bio-Rad (Bio-Rad Laboratories, Inc., Hercules, CA, USA) and multiplex analysis was performed on a Bio-Plex 100 system (Bio-Rad). Assays were performed according to manufacturer’s instructions. Briefly, plasma was diluted 1:2 and incubated with antibody-coupled beads. Complexes were washed and then incubated with biotinylated detection antibody followed by streptavidin-phycoerythrin prior to assessing titers of cytokine concentration. Recombinant cytokines were used to establish standard curves. Analyte concentrations were calculated using the Bio-Plex Manager 4.0 Software (Bio-Rad).
Measurement of skeletal muscle injury
An ELISA kit for measuring skeletal muscle creatine kinase (CK-MM, from USCN Life Sciences, Wuhan, China) was used to measure skeletal muscle injury. The assay was performed according to the manufacturers' protocol and samples were analyzed in duplicates for each time point. Concentrations were determined by comparing with standards provided with the kit.
All data was initially checked for normality by Kolmogorov-Smirnov test. Time dependant changes were tested by Repeated Measures ANOVA test with confidence interval set to 95%. Bonferroni's multiple comparison test was used as a post test. When only two time points had to be statistically compared, two tailed paired t-test was used with the level of significance set to 95%. All statistics calculations were done in Prism 4.0a for Macintosh (GraphPad Software, Inc., La Jolla, CA, USA).
The average tourniquet time for the 10 patients was 116 ± 16 minutes.
Shedding of glycocalyx and EC integrity/activation
Immunofluorescence staining for markers of EC integrity / activation
Markers of EC integrity / activation
10 min reperfusion
0.45 ± 0.16*
0.44 ± 0.14
0.58 ± 0.11
0.34 ± 0.37
0.64 ± 0.64
0.60 ± 0.49
2.20 ± 3.99
0.61 ± 0.83
0.51 ± 0.57
Binding of antibodies and activation of complement system
Immunofluorescence staining for markers of complement activation
Antibody and complement deposition in tissue
10 min reperfusion
1.03 ± 9.60*
0.81 ± 0.60
0.50 ± 0.40
0.02 ± 0.02
0.06 ± 0.08
0.03 ± 0.03
0.12 ± 0.13
0.12 ± 0.22
0.13 ± 0.22
0.16 ± 0.10
0.29 ± 0.46
0.22 ± 0.31
Skeletal muscle injury
As an interface between the circulating blood and tissue it is not difficult to consider the EC to react immediately to pathophysiological processes during I/R. An important reaction of the endothelium is the shedding of its native, anticoagulant and anti-inflammatory surface layer, the glycocalyx . The latter is composed mainly of heparan sulfate proteoglycans, among which syndecans as core proteins . We therefore measured the levels of shed heparan sulfate, syndecan-1 in serum and expression of HSPG on tissue, which showed no changes from baseline to 10 min reperfusion. Together, these data support the notion that no significant activation of EC occurred in our setting of tourniquet-induced ischemia and reperfusion. This finding is in contrast to earlier reports, for example on patients undergoing coronary artery bypass grafting under extracorporeal circulation, where increased serum levels of syndecan-1 and HS were found as early as after 2 min of reperfusion . In the latter study, however, the tubings and filters in the extracorporeal circulation circuit, which are known to lead to complement activation, may account for at least part of the observed EC activation.
Other markers of EC activation documented previously are CD31 and vWF [23, 24], and we included detection of these antigens on tissue biopsies by immunostaining. Earlier studies by Huhges et al. [25, 26], showed no significant increase in vWF plasma levels after 10 min and 30 min of ischemia and 15 min and 30 min reperfusion, respectively. Our study confirms this finding with no significant changes in vWF and CD31 expression in biopsies, which further indicate minimal EC activation or damage during early reperfusion. However, the study does not consider differences in the constitutive expression patterns of these antigens, which could vary due to heterogeneity in vessel size as shown for vWF .
Previous studies on murine skeletal muscle I/R injury models have identified natural IgM antibodies as a major initiator of the activation of the complement system, which was also shown to be causally related to the observed tissue injury . We therefore analyzed deposition of IgM as well as IgG in the tissue. However, no significant differences between ischemia and reperfusion samples were found for these antibody isotypes. In line with the absence of antibody deposition, markers for complement activation C3b/c, C4b/c on tissue and C3a, C4d in plasma did not change until 10 min reperfusion. This suggests that no significant activation of the complement system occurred in our setting of tourniquet-induced ischemia and reperfusion injury. Also the levels of functional C1-inhibitor, which is the only known physiologic inhibitor of classical complement pathway activation , showed no changes from baseline to 10 min reperfusion.
Pro-inflammatory cytokines are secreted to preserve immune integrity and stimulate repair mechanisms to counteract the ongoing tissue damage [29, 30]. The pro-inflammatory cytokines IL-1 and TNFα in particular are released by monocytes and macrophages during the acute phase of I/R injury and in turn stimulate the production of IL-6 . In our study we found that TNFα and IL-6 were significantly elevated in serum at 10 min reperfusion as compared to baseline. This result is in line with two reports of tourniquet application in lower limb surgery, where a rise in IL-6 was shown at 2 h and 4 h reperfusion, respectively, in the draining blood of the ischemic limbs [19, 32]. We also found a significant rise in the levels of IL-17 from baseline, highlighting the involvement of another pro-inflammatory molecule, which is known to induce EC to secrete cytokines.
Among the cytokines secreted by EC, IL-7 showed a significant rise in the 10 minutes reperfusion sample, but this was not the case for IL-8. Predominantly anti-inflammatory cytokines like IL-10 and IL-5 did not show any significant changes at 10 min reperfusion.
To our knowledge, the role of MCP-1 has not yet been studied in human skeletal muscle I/R injury. Studies on MCP-1 in other models have shown its involvement in both inflammation  and muscle regeneration . Our data show no significant changes in the levels of MCP-1 until 10 min of reperfusion. On the other hand, an increased level of GM-CSF, but not of G-CSF, was found, probably due to the recruitment of monocytes at the site of ischemia.
VEGF  and PDGF bb  are growth factors that help in angiogenesis and formation of new blood vessels and are induced as a response to ischemia. In the present study we could also show this type of vascular responses to ischemia by significantly higher plasma levels of VEGF and PDGF bb at 10 min reperfusion.
Finally, CK-MM was measured as a marker for skeletal muscle injury . The observed significant rise of the enzyme levels at end of ischemia (0 min reperfusion) as well as at 10 min reperfusion when compared to baseline indicates that a certain level of skeletal muscle injury is occurring in our model, despite the apparent absence of activation of complement and EC.
Clinical significance of the study
As mentioned previously the use of tourniquet on a limb renders it to the risk of I/R injury which clinically manifests as pain, swelling, prolonged hypoesthesia of peripheral nerves, tissue necrosis along with systemic effects. For the formation of edema, which may lead to the feared compartment syndrome, EC activation and damage are key events. Their absence during the very early reperfusion phase (as shown in our study) may offer a window of opportunity to protect the endothelium and thus to prevent further reperfusion injury, for example by local use of endothelial cell protective substances which proved to be effective to prevent I/R injury in experimental myocardial infarction [38, 39].
Conclusions and limitations
The aim of this study was to assess the endothelium and the inflammatory response during the early phase of reperfusion. In this clinical model of tourniquet induced I/R injury, we show an active involvement of the inflammatory cascade with a rise in cytokines, mainly TNFα, IL-6, IL-17, IL-7, GM-CSF, PDGF bb and VEGF, during early reperfusion. Additionally a rise in CK-MM was observed indicating a certain degree of skeletal muscle injury post surgery. However, in contrast to our original hypothesis, no significant activation of EC or the complement system could be observed until 10 min reperfusion.
A limitation of the study is that we cannot account for the source of the increased cytokine production as observed, which could be local or systemic. Additional analysis of the same parameters in samples taken from the systemic circulation would have been helpful. The short follow-up of only 10 min during the reperfusion phase is a limitation of the study. Clinically, edema becomes apparent only several hours after surgery and additional studies with analyses of plasma samples after reperfusion times of 6 h or more need to be done. Another limitation of the study is the ischemia period with a rather wide standard deviation and the varying clinical background and underlying diseases of the patients. However, there is no scope for standardization of these two parameters in a clinical setting like the current study, and more uniform experiments in this direction will have to be conducted in animal models.
This study was supported by the Inselspital, Bern University Hospital (study no. 1711) and the Swiss National Science Foundation (3200B0-116618 and 32003B-135272). We would like to thank Prof. Hans Imboden, University of Bern, for support with the free float staining technique, Dr. Mathias Traub for his help with patient-related work and Mrs. Katja Matozan for technical support in the project.
- Van Teeffelen JW, Brands J, Stroes ES, Vink H: Endothelial glycocalyx: sweet shield of blood vessels. Trends Cardiovasc Med. 2007, 17: 101-105. 10.1016/j.tcm.2007.02.002.View ArticlePubMedGoogle Scholar
- Mulivor AW, Lipowsky HH: Inflammation- and ischemia-induced shedding of venular glycocalyx. Am J Physiol Heart Circ Physiol. 2004, 286: H1672-H1680. 10.1152/ajpheart.00832.2003.View ArticlePubMedGoogle Scholar
- Ward BJ, Donnelly JL: Hypoxia induced disruption of the cardiac endothelial glycocalyx: implications for capillary permeability. Cardiovasc Res. 1993, 27: 384-389. 10.1093/cvr/27.3.384.View ArticlePubMedGoogle Scholar
- Shibata S, Sasaki T, Harpel P, Fillit H: Autoantibodies to vascular heparan sulfate proteoglycan in systemic lupus erythematosus react with endothelial cells and inhibit the formation of thrombin-antithrombin III complexes. Clin Immunol Immunopathol. 1994, 70: 114-123. 10.1006/clin.1994.1018.View ArticlePubMedGoogle Scholar
- Wang L, Fuster M, Sriramarao P, Esko JD: Endothelial heparan sulfate deficiency impairs L-selectin- and chemokine-mediated neutrophil trafficking during inflammatory responses. Nat Immunol. 2005, 6: 902-910.View ArticlePubMedGoogle Scholar
- Tanaka Y, Kimata K, Adams DH, Eto S: Modulation of cytokine function by heparan sulfate proteoglycans: sophisticated models for the regulation of cellular responses to cytokines. Proc Assoc Am Physicians. 1998, 110: 118-125.PubMedGoogle Scholar
- Rehm M, Bruegger D, Christ F, Conzen P, Thiel M, Jacob M, Chappell D, Stoeckelhuber M, Welsch U, Reichart B: Shedding of the endothelial glycocalyx in patients undergoing major vascular surgery with global and regional ischemia. Circulation. 2007, 116: 1896-1906. 10.1161/CIRCULATIONAHA.106.684852.View ArticlePubMedGoogle Scholar
- Austen WG, Zhang M, Chan R, Friend D, Hechtman HB, Carroll MC, Moore FD: Murine hindlimb reperfusion injury can be initiated by a self-reactive monoclonal IgM. Surgery. 2004, 136: 401-406. 10.1016/j.surg.2004.05.016.View ArticlePubMedGoogle Scholar
- Zhang M, Alicot EM, Chiu I, Li J, Verna N, Vorup-Jensen T, Kessler B, Shimaoka M, Chan R, Friend D: Identification of the target self-antigens in reperfusion injury. J Exp Med. 2006, 203: 141-152. 10.1084/jem.20050390.PubMed CentralView ArticlePubMedGoogle Scholar
- Banz Y, Rieben R: Role of complement and perspectives for intervention in ischemia-reperfusion damage. Ann Med. 2012, 44: 1-13. 10.3109/07853890.2010.532150.View ArticleGoogle Scholar
- Mohler LR, Pedowitz RA, Lopez MA, Gershuni DH: Effects of tourniquet compression on neuromuscular function. Clin Orthop Relat Res. 1999, 359: 213-220.View ArticlePubMedGoogle Scholar
- Lin LN, Wang LR, Wang WT, Jin LL, Zhao XY, Zheng LP, Jin LD, Jiang LM, Xiong XQ: Ischemic preconditioning attenuates pulmonary dysfunction after unilateral thigh tourniquet-induced ischemia-reperfusion. Anesth Analg. 2010, 111: 539-543. 10.1213/ANE.0b013e3181e368d2.View ArticlePubMedGoogle Scholar
- Smith TO, Hing CB: The efficacy of the tourniquet in foot and ankle surgery? A systematic review and meta-analysis. Foot Ankle Surg. 2010, 16: 3-8. 10.1016/j.fas.2009.03.006.View ArticlePubMedGoogle Scholar
- Girardis M, Milesi S, Donato S, Raffaelli M, Spasiano A, Antonutto G, Pasqualucci A, Pasetto A: The hemodynamic and metabolic effects of tourniquet application during knee surgery. Anesth Analg. 2000, 91: 727-731. 10.1213/00000539-200009000-00043.View ArticlePubMedGoogle Scholar
- Sapega AA, Heppenstall RB, Chance B, Park YS, Sokolow D: Optimizing tourniquet application and release times in extremity surgery. A biochemical and ultrastructural study. J Bone Joint Surg Am. 1985, 67: 303-314.PubMedGoogle Scholar
- Lindsay T, Romaschin A, Walker PM: Free radical mediated damage in skeletal muscle. Microcirc Endothelium Lymphatics. 1989, 5: 157-170.PubMedGoogle Scholar
- Germann G, Drucke D, Steinau HU: Adhesion receptors and cytokine profiles in controlled tourniquet ischaemia in the upper extremity. J Hand Surg Br. 1997, 22: 778-782. 10.1016/S0266-7681(97)80447-0.View ArticlePubMedGoogle Scholar
- Sutter PM, Spagnoli GC, Marx A, Gurke L, Troeger H, Fricker R, Harder F, Heberer M: Increased surface expression of CD18 and CD11b in leukocytes after tourniquet ischemia during elective hand surgery. World J Surg. 1997, 21: 179-184. 10.1007/s002689900212. discussion 185View ArticlePubMedGoogle Scholar
- Huda R, Solanki DR, Mathru M: Inflammatory and redox responses to ischaemia/reperfusion in human skeletal muscle. Clin Sci (Lond). 2004, 107: 497-503. 10.1042/CS20040179.View ArticleGoogle Scholar
- Gute DC, Ishida T, Yarimizu K, Korthuis RJ: Inflammatory responses to ischemia and reperfusion in skeletal muscle. Mol Cell Biochem. 1998, 179: 169-187. 10.1023/A:1006832207864.View ArticlePubMedGoogle Scholar
- Chappell D, Hofmann-Kiefer K, Jacob M, Rehm M, Briegel J, Welsch U, Conzen P, Becker BF: TNF-alpha induced shedding of the endothelial glycocalyx is prevented by hydrocortisone and antithrombin. Basic Res Cardiol. 2009, 104: 78-89. 10.1007/s00395-008-0749-5.View ArticlePubMedGoogle Scholar
- Morgan MR, Humphries MJ, Bass MD: Synergistic control of cell adhesion by integrins and syndecans. Nat Rev Mol Cell Biol. 2007, 8: 957-969. 10.1038/nrm2289.PubMed CentralView ArticlePubMedGoogle Scholar
- Woodfin A, Voisin MB, Imhof BA, Dejana E, Engelhardt B, Nourshargh S: Endothelial cell activation leads to neutrophil transmigration as supported by the sequential roles of ICAM-2, JAM-A, and PECAM-1. Blood. 2009, 113: 6246-6257. 10.1182/blood-2008-11-188375.PubMed CentralView ArticlePubMedGoogle Scholar
- Datta YH, Ewenstein BM: Regulated secretion in endothelial cells: biology and clinical implications. Thromb Haemost. 2001, 86: 1148-1155.PubMedGoogle Scholar
- Hughes SF, Hendricks BD, Edwards DR, Bastawrous SS, Roberts GE, Middleton J, Hughes SF, Hendricks BD, Edwards DR, Bastawrous SS, Roberts GE, Middleton JF: Mild episodes of tourniquet-induced forearm ischaemia-reperfusion injury results in leukocyte activation and changes in inflammatory and coagulation markers. J Inflamm (Lond). 2007, 4: 12-10.1186/1476-9255-4-12.View ArticleGoogle Scholar
- Hughes SF, Hendricks BD, Edwards DR, Middleton JF: Tourniquet-applied upper limb orthopaedic surgery results in increased inflammation and changes to leukocyte, coagulation and endothelial markers. PLoS One. 2010, 5: e11846-10.1371/journal.pone.0011846.PubMed CentralView ArticlePubMedGoogle Scholar
- Liu J, Yuan L, Molema G, Regan E, Janes L, Beeler D, Spokes KC, Okada Y, Minami T, Oettgen P, Aird WC: Vascular bed-specific regulation of the von Willebrand factor promoter in the heart and skeletal muscle. Blood. 2011, 117: 342-351. 10.1182/blood-2010-06-287987.PubMed CentralView ArticlePubMedGoogle Scholar
- Storini C, Rossi E, Marrella V, Distaso M, Veerhuis R, Vergani C, Bergamaschini L, De Simoni MG: C1-inhibitor protects against brain ischemia-reperfusion injury via inhibition of cell recruitment and inflammation. Neurobiol Dis. 2005, 19: 10-17. 10.1016/j.nbd.2004.11.001.View ArticlePubMedGoogle Scholar
- Ferencik M: Molecular and cellular mechanisms in inflammatory reactions. Bratisl Lek Listy. 1995, 96: 509-519.PubMedGoogle Scholar
- Ferencik M, Stvrtinova V: Endogenous control and modulation of inflammation. Folia Biol (Praha). 1996, 42: 47-55.Google Scholar
- Akira S, Isshiki H, Nakajima T, Kinoshita S, Nishio Y, Natsuka S, Kishimoto T: Regulation of expression of the interleukin 6 gene: structure and function of the transcription factor NF-IL6. CIBA Found Symp. 1992, 167: 47-62. discussion 62–47PubMedGoogle Scholar
- Clementsen T, Reikeras O: Cytokine patterns after tourniquet-induced skeletal muscle ischaemia reperfusion in total knee replacement. Scand J Clin Lab Invest. 2008, 68: 154-159. 10.1080/00365510701528587.View ArticlePubMedGoogle Scholar
- Lu B, Rutledge BJ, Gu L, Fiorillo J, Lukacs NW, Kunkel SL, North R, Gerard C, Rollins BJ: Abnormalities in monocyte recruitment and cytokine expression in monocyte chemoattractant protein 1-deficient mice. J Exp Med. 1998, 187: 601-608. 10.1084/jem.187.4.601.PubMed CentralView ArticlePubMedGoogle Scholar
- Shireman PK, Contreras-Shannon V, Ochoa O, Karia BP, Michalek JE, McManus LM: MCP-1 deficiency causes altered inflammation with impaired skeletal muscle regeneration. J Leukoc Biol. 2007, 81: 775-785.View ArticlePubMedGoogle Scholar
- Cherwek DH, Hopkins MB, Thompson MJ, Annex BH, Taylor DA: Fiber type-specific differential expression of angiogenic factors in response to chronic hindlimb ischemia. Am J Physiol Heart Circ Physiol. 2000, 279: H932-H938.PubMedGoogle Scholar
- Iihara K, Sasahara M, Hashimoto N, Uemura Y, Kikuchi H, Hazama F: Ischemia induces the expression of the platelet-derived growth factor-B chain in neurons and brain macrophages in vivo. J Cereb Blood Flow Metab. 1994, 14: 818-824. 10.1038/jcbfm.1994.102.View ArticlePubMedGoogle Scholar
- Wu AH, Perryman MB: Clinical applications of muscle enzymes and proteins. Curr Opin Rheumatol. 1992, 4: 815-820.PubMedGoogle Scholar
- Banz Y, Hess OM, Robson SC, Mettler D, Meier P, Haeberli A, Csizmadia E, Korchagina EY, Bovin NV, Rieben R: Locally targeted cytoprotection with dextran sulfate attenuates experimental porcine myocardial ischaemia/reperfusion injury. Eur Heart J. 2005, 26: 2334-2343. 10.1093/eurheartj/ehi421.View ArticlePubMedGoogle Scholar
- Banz Y, Hess OM, Robson SC, Csizmadia E, Mettler D, Meier P, Haeberli A, Shaw S, Smith RA, Rieben R: Attenuation of myocardial reperfusion injury in pigs by Mirococept, a membrane-targeted complement inhibitor derived from human CR1. Cardiovasc Res. 2007, 76: 482-493. 10.1016/j.cardiores.2007.07.016.View ArticlePubMedGoogle Scholar
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