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1 Department of Transfusion Medicine, University of Tuebingen, D-72076 Tuebingen; and 2 Medical Clinic and Polyclinic, Department of Sports Medicine, University of Tuebingen, D-72074 Tuebingen, Germany
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ABSTRACT |
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 TOP
 ABSTRACT
 INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES
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Heat shock proteins (HSP) represent cell-protective and antioxidant systems that may be induced by reactive oxygen species, cytokines, and hyperthermia. In the present study, we evaluated the influence of heavy endurance exercise and training on HSP27 and HSP70 in peripheral leukocytes of 12 athletes (before and at 0, 3, and 24 h after a half-marathon) and 12 untrained controls on protein and mRNA levels by flow cytometry and RT/PCR, respectively. HSP transcripts increased significantly immediately after acute exertion accompanied by elevated levels of corresponding proteins. HSP protein expression remained high until 24 h postexercise. Significant increases of plasma interleukin-8, myeloperoxidase, and creatine kinase occurred after exercise. Basal HSP expression was usually lower in trained compared with untrained subjects. Applying in vitro heat shock to resting blood samples of all subjects significantly stimulated HSP mRNA, showing higher increases in trained individuals. The exercise-induced alterations indicate that immunocompetent cells became activated. In addition to heat stress, other exercise-associated stress agents (oxidants, cytokines) may have also participated in stimulation of HSP expression in leukocytes. The expression pattern of HSP due to training status may be attributed to adaptive mechanisms.
oxidative; stress; cytokine; mRNA; exercise
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INTRODUCTION |
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TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES
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STRENUOUS PHYSICAL
EXERCISE has been shown to induce an acute response of the immune
system, including the activation of inflammatory cells
(17, 22). Metabolic activation correlates
with an augmented generation of reactive oxygen species (ROS) and
reactive nitrogen intermediates by leukocytes, a mechanism that is
partly mediated by cytokines such as plasma interleukin-8 (IL-8) and
tumor necrosis factor-
(TNF-) (2, 31,
32). Protection and/or tolerance against exercise-induced
oxidative, heat, cytokine, and inflammatory stress in leukocytes may be
in part provided by heat shock proteins (HSPs) (7). The
metabolic changes caused by exercise are similar to those known to
induce stress protein synthesis (8, 12). HSPs
play a role in protein translocation, stabilization, assembly, and
degradation processes, functions that could be important in leukocytes
activated by heavy exercise (10, 11,
27).
The question arose whether strenuous exercise such as a half-marathon influences HSP expression in blood at the cellular, protein, and/or transcriptional level. Semiquantitative RT/PCR and flow cytometry were used for analysis of HSP27 and HSP70 alterations in leukocytes due to strenuous endurance exercise. We used a competitive half-marathon as an in vivo stress model. Furthermore, we intended to verify whether the regulation of basal HSP expression in immunocompetent cells exhibits adaptation due to regular endurance training. A control group of untrained men at rest was compared with half-marathon runners at rest to examine the influence of regular endurance training on the baseline expression of HSPs in leukocytes. In vitro stimulation of leukocytes with heat shock was used to evaluate the individual heat shock response to a defined stimulus in differently trained subjects.
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MATERIALS AND METHODS |
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TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES
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Twelve well-trained male athletes (53.3 ± 18.4 km/wk running; 32.3 ± 9.3 yr; 175.0 ± 3.3 cm; 64.4 ± 3.7 kg) performed an official half-marathon under competition conditions (21.1 km), which started at 10:00 AM on a cool and humid December day (1°C). Venous blood samples were taken with the subjects in a sitting position with EDTA used as anticoagulant. The samples were collected at rest 24 h before (9:00 AM), directly after (11:30 AM-12:00 noon), and 3 h (2:30-3:00 PM) and 24 h (9:00 AM) after competition. The trained individuals were engaged in specific endurance training. During the last 3 days before the race, the athletes performed only moderate endurance runs lasting up to 40 min with a running intensity below the lactate threshold. Athlete 8 did not finish the half-marathon due to a knee injury; his postexercise values were excluded from the statistics. Additionally, blood samples obtained at rest from 12 healthy and normally conditioned male adults, who did not participate in the half-marathon, were collected (9:00 AM) as sedentary control (45.4 ± 11.4 yr; 176.7 ± 2.8 cm; 75.9 ± 3.2 kg). These untrained individuals did not perform any kind of sports conditioning and did not have any stress situation during the 3 days before the collection of blood samples. The preexercise samples of the trained persons represent the corresponding resting (baseline) value. None of the subjects used drugs or mineral or vitamin supplements. Each gave written informed consent before participation in the study. The experimental protocol was approved by the institute's human ethics committee according to the principles set forth in the Declaration of Helsinki of the World Medical Association.
Analytic methods. The lactate concentrations of the hemolyzed capillary blood samples were measured electrochemically by use of a lactate analyzer (EBIO, Eppendorf, Hamburg, Germany). Plasma creatine kinase (CK) activity and uric acid concentrations were determined by enzymatic analyses (Hitachi 717, Boehringer, Mannheim, Germany).
Hematocrit, hemoglobin concentration, and total and differential counts of white blood cells were determined by using an automated hematology analyzer (Coulter Juniors JS, Coulter Electronics). Differential analyses of lymphocytes, monocytes, and neutrophils were conducted automatically. Hematocrit and hemoglobin were used to correct plasma concentration of CK, myeloperoxidase (MPO), IL-8, and TNF- with
regard to changes in plasma volume after exercise (6).
Preparation of leukocytes from peripheral blood for flow cytometry. Five milliliters of EDTA blood were carefully layered over 5 ml of Lymphoflot (Biotest, Dreieich, Germany), a solution containing diatrizoate (9.6% wt/vol) and Ficoll (5.6% wt/vol), and allowed to settle by gravity without centrifugation for 60 min. The erythrocytes were aggregated at the interface and sedimented to the bottom of the tube. The majority of the leukocytes remained in the plasma layer and were removed. The overlay was washed two times with PBS, and the cell concentration was adjusted with PBS to 1 × 107 cells/ml; 100 µl of the suspension was used for analysis by flow cytometry.
Flow cytometry. The cells were analyzed by intracellular, indirect immunofluorescence by using HSP-specific monoclonal antibodies (StressGen, Biotechnologies, Victoria, BC, Canada; Biomol, Hamburg, Germany): SPA-800 (HSP27; IgG1, clone G3.1) and SPA-810 (specific for the inducible form of human HSP70; IgG1, clone C92F3A-5).
Cells (1 × 106) were first fixed at room temperature in a solution containing formaldehyde (reagent A) according to the manufacturer's instructions (Fix & Perm kit, An der Grub, Vienna, Austria) and washed twice. Then the cells were permeabilized with reagent B and at the same time incubated with the primary HSP-specific monoclonal antibody shown to give the maximum of positive cells or isotype-matched monoclonal antibodies at the same concentration (1 µg/test) and incubated for 15 min at room temperature. After washing the cells twice and incubating in the presence of the secondary FITC-conjugated goat anti-mouse F(ab')2 IgG (Dianova, Hamburg, Germany), we analyzed the cells using the flow cytometer EPICS-XL-MLC (Coulter, Krefeld, Germany). Dead cells were excluded by electronic gating, and fluorescence histograms were area corrected to 10,000 cells. The lymphocyte, monocyte, and granulocyte populations were differentiated according to granularity and size in the forward vs. side scattergram and were gated. For each of the three special gates, data were presented as percent positive cells and mean fluorescent channel (MFC), corrected for background fluorescence by the negative controls.Isolation of RNA and RT/PCR.
Cytoplasmic RNA for RT/PCR analyses was isolated from whole blood with
the RNeasy-blood kit (Qiagen, Hilden, Germany). Three hundred nanograms
of RNA were reverse transcribed (10' 20°C; 15' 42°C; 5' 99°C; 5'
5°C) and amplified (3' 95°C; 1' 95°C; 1' 55°C; 1' 72°C) in
the thermal cycler (MJ Research, PTC200) using specific primers for
HSP27 and HSP70B [StressGen, Biotechnologies, (38)] and
for 
-actin (34). RT and subsequent amplification by the PCR were performed by using a GeneAmp RNA PCR kit (Perkin-Elmer). The
RT master mix contained 10 mM Tris·HCl, pH 8.3; 50 mM KCl; 5 mM
MgCl2; 1 mM each of deoxyribonucleoside triphosphates, 1 U/µl RNase inhibitor; 2.5 U/µl RT; and 2.5 µl of oligo(dT). The final RT reaction volume was 20 µl. The PCR master mix contained 50 mM KCl; 10 mM Tris-HCl, pH 8.3; 1.25 mM MgCl2; 200 µM
each of deoxyribonucleoside triphosphates; 2.5 U/100 µl AmpliTaq DNA polymerase; and 0.15 µM of each primer. A final 25 µl of PCR
reaction solution contained 5 µl RT product (cDNA) and 20 µl PCR
master mix. For each primer pair, control experiments were performed to
determine the range of cycles in which a given amount of cDNA would be
amplified in a linear fashion: HSP27, 25 cycles; HSP70, 30 cycles; and
actin, 27 cycles. Furthermore, a dilution assay was performed to
determine the proper input RNA concentration. The resulting amplified
products for HSP27 (285 bp) and HSP70B (234 bp) were confirmed by
sequence analysis (SEQLAB, Goettingen, Germany). Photographs of
ethidium bromide-stained DNA gels (2%) were scanned by the
Lumi-Imager-System (Boehringer), which allowed semiquantitative
analyses of the specific HSP27 and HSP70 expression. The data generated
were normalized to transcript levels for the constitutively expressed
-actin gene.
In vitro stimulation with heat shock. EDTA blood of 12 healthy, normally conditioned (untrained) male adults at rest and of 12 well-trained athletes at rest was incubated for 2 h in a water bath heated to 42°C (heat shock). Experimental heat shock conditions were chosen to induce an intensive stress response in vitro without cell damage (8, 13, 27). The heat-shocked blood samples were prepared for further analyses as described above. Control blood samples of the same persons were treated identically except for the heat shock exposure.
ELISA.
Testing for IL-8 (Genzyme, Duoset, Cambridge, MA, 1.0 pg/ml), TNF-
(R&D Systems, Minneapolis, MN, 1.0 pg/ml), and MPO
(Calbiochem-Novabiochem, Bad Soden, Germany, 1.5 pg/ml) in the plasma
samples of the athletes was done by ELISA according to the instructions
of the manufacturer.
Statistical methods.
All statistical analyses and descriptional methods were computed by the
statistical software package JMP (JMP3.1 software, SAS Institute, Cary,
NC) for personal computer. Data in Tables 1-3
are expressed as means ± SD. Comparisons of repeated measurements in the trained athletes were tested for significance by the Wilcoxon signed-ranks test. The nonparametric test of Mann-Whitney was used for
evaluation of significant differences between the resting values and
the heat shock-induced increases of the trained and untrained group. A
P value of P < 0.05 was regarded as
significant.
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RESULTS |
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TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES
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Leukocyte, monocyte, and granulocyte counts were significantly increased after exercise and declined 24 h later to baseline levels (P < 0.05). By contrast, lymphocyte counts decreased 3 h after the run (P < 0.05, Table 1). Leukocyte counts of untrained controls at rest were 5.3 ± 1.4 × 109/l.
CK was also significantly increased and had its maximum 24 h postexercise (P < 0.05, Table 1). Lactate values after exercise were 5.1 ± 2.2 mmol/l.
MPO and IL-8 in plasma were significantly stimulated directly after
exercise and were normalized thereafter (P < 0.05, Table 1). An elevation of TNF- immediately and 3 h after the
run could be detected, but only single samples attained values above
the detection limit of 1.0 pg/ml (Table 1).
RT/PCR.
Semiquantitative RT/PCR analyses revealed a significantly stimulated
mRNA-expression of HSP27 (P < 0.05) and HSP70 in
leukocytes of all athletes directly after the half-marathon (0 h)
compared with preexercise levels (rest) (Figs.
1 and 2).
In individual athletes, elevated levels of HSP70 transcript could be
detected even 3 h after the competition. After 24 h, the
values decreased to near preexercise levels.
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-actin cDNAs were amplified under conditions to
allow relative comparisons for a given mRNA species.
The comparison of trained vs. untrained persons revealed different HSP
mRNA expression. Baseline HSP27 transcripts were significantly downregulated in leukocytes of athletes, whereas the HSP70 mRNA expression was significantly higher in trained compared with untrained men (P < 0.05, Figs. 3
and 4).
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Flow cytometric analyses. After the race, there was a significantly greater percentage of leukocytes expressing cytoplasmic HSP27 and HSP70 (P < 0.05, Table 2). The fluorescence intensity increased significantly in monocytes for HSP27 (0 h and 3 h, P < 0.05) and for HSP70 (0 h, 3 h, and 24 h, P < 0.05) (Table 2). In granulocytes, the HSP70 MFC was only stimulated 24 h postexercise (P < 0.05). The further increase 24 h after the run, which was detectable in all HSP70 values and only HSP27-positive granulocytes (Table 2), is remarkable. Lymphocytes were mainly negative for HSP.
Counts of HSP27- and HSP70-positive mono- and granulocytes of trained athletes were significantly lower compared with the corresponding cells of untrained persons (P < 0.05, Table 3).| |
DISCUSSION |
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TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
REFERENCES
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The changes in cell counts and increases in MPO, IL-8, TNF-,
and CK in plasma reflect activation of immunocompetent cells as well as
oxidative, cytokine, and muscular stress due to the half-marathon
(1, 4, 25, 29,
35). This exercise-induced stress response may contribute
to the induction of HSP in leukocytes of athletes after intensive
endurance exercise, which we investigated in this study at the mRNA and
protein level.
Influence of acute strenuous exercise on HSP expression. In our study, we described that strenuous endurance exercise such as a half-marathon stimulated HSP27 and HSP70 expression in leukocytes of human subjects at pretranslational and protein levels detected by RT/PCR and flow cytometry, respectively. HSP may play a protective role in leukocytes against exercise-induced stress, prepare them to survive new environmental challenges, and maintain cellular homeostasis. The increase in HSP expression is accompanied by the maintenance of the proliferative capacity and viability of the cells (13). HSP could further indicate selective mechanisms in protein conservation, regulation of the inflammatory response, and receptor function. HSPs are activated on cellular stress/injury and oxidative, heat, and cytokine stress and participate in the folding and intracellular transport of damaged proteins (7, 11).
The differential regulation of HSP mRNA expression, percent HSP-positive cells, and their MFC intensity started with an initial increase of HSP mRNA in the leukocytes immediately after the half-marathon. It was partially paralleled and followed by a prolonged high (0- to 3-h) protein expression level, mainly in monocytes. The deficiency of MFC increase in granulocytes in the first hours after exercise may be the result of less HSP-specific transcriptional and/or translational activation, potentially due to the short half-life of granulocytes. The stimulation of all HSP-positive cell populations lasted longer and even increased 24 h after exercise. The changes reflect activation of immunocompetent cells, particularly mono- and granulocytes, cells that are capable of producing relevant quantities of ROS as a result of their activation under physical stress (18). A systemic neutrophil activation and degranulation due to the half-marathon was also mirrored in a rise in plasma MPO (1). Together with the parallel, significant increase of IL-8, this is likely the basis for exercise-induced generation of ROS, which may partly be responsible for the HSP reaction. The delayed augmentation of HSP-positive cell counts may arise from an accumulation of activated cells, increased recruitment of the periphery, lower degradation processes, or an activation of the cells due to late effects of muscular stress. The late changes in HSP-positive cells were not reflected at the mRNA level. Although the preparation of cytoplasmic mRNA consisted mainly of granulocytes, there was no correlation between granulocyte counts and HSP mRNA expression. An inflammatory response originating from muscular stress after exercise may be in part responsible for the activation of immunocompetent cells in the peripheral blood. The CK values, a marker of muscular stress, showed enhanced values 24 h postexercise. Hyperthermia and metabolic stress (lactate increase, glycogen depletion) may be additional reasons for HSP induction after heavy exercise (8, 12, 28). The exercise-induced activation of leukocytes may be mediated by acute-phase proteins or oxidative stress due to a systemic inflammatory reaction. TNF-, a proinflammatory cytokine, and IL-8, a marker of
oxidative stress, were stimulated in plasma as a result of the
half-marathon run in this study. An increase of TNF-, interleukin-6,
and interferon-
after intensive endurance exercise has already been
described by several authors (20, 21,
36). Parallel increases of HSP expression, TNF-, and
IL-8 after the half-marathon point to a conceivable relationship
between cytokines and HSP induction in immunocompetent cells. The
pronounced rise especially of IL-8, linked to ROS and reactive nitrogen
intermediate production (25, 33), implies
oxidative stress as a possible stimulator of HSP expression. A
correlation recently detected in leukocytes between the antioxidative
stress protein heme oxygenase-1 and IL-8 after a half-marathon
(19) confirms our association of exercise-induced activation of immunocompetent cells, followed by oxidative and cytokine
stress, resulting in HSP induction.
In vitro heat shock. The exposure of peripheral blood to in vitro heat shock revealed significant effects on HSP mRNA expression. As expected, HSP transcripts were significantly stimulated by heat shock in vitro (30) similar to the effects elicited by exercise-induced stress. Nevertheless, it seems probable that HSPs in leukocytes were synthesized as a result of multiple mechanisms associated with exercise stress, including oxidative, cytokine, and muscular stress, and not only as a result of exercise-induced hyperthermia per se.
It is noteworthy that the heat shock-induced stimulation of HSP mRNA expression was significantly more pronounced in leukocytes of trained compared with untrained individuals. Regular endurance training seems to affect protective mechanisms in immunocompetent cells beneficially. The enhanced heat shock response in the athletes at rest may represent an activation of the protective resources in immune cells from denaturing heat. It may be interpreted as a training-induced mechanism of adaptation or as acquired thermotolerance (7, 15).Training-related effects. The basal HSP expression of the trained athletes at rest displayed a unique pattern, different from that of nontrained individuals. HSP27- and HSP70-positive mono- and granulocytes were significantly diminished in trained compared with untrained persons. HSP27 transcripts were also decreased in the trained subjects, but HSP70 mRNA expression was significantly increased. The decrease in HSP expression may be explained by a lower pro-oxidant state due to intensive training, which is described by several authors (3, 9, 14, 24, 26). Nevertheless, the low HSP27 and the high HSP70 mRNA levels could both be significantly stimulated by a maximal stress such as a half-marathon or by heat shock in vitro, and the mRNAs were also translated, resulting in an enlargement of HSP-positive cells. The higher baseline expression of HSP70 mRNA in athletes as a result of intensive training may be attributed to a unique characteristic of HSP70 mRNA, which is unstable under normal physiological conditions and stabilizes under stress conditions (23). This may also be a mechanism of adaptation to regular, intensive endurance training. One can speculate that the training-stressed cells provide high HSP70 transcript levels for immediate translation whenever necessary. The resulting accumulation of HSP70 proteins themselves may regulate translation via a negative-feedback loop if they are not used for an immediate stress response (5, 16, 37).
The exact function of the differential regulation of HSP at the transcriptional and translational level in response to exercise and to experimental heat stress, as observed in our study, remains to be investigated further. Exercise-induced oxidative, cytokine, and heat stress may be involved in the stress response reported here. The results are potentially valid to monitor beneficial or unfavorable effects of intensive endurance exercise or extensive training and to estimate the relevance of individual stress gene responses in circulating leukocytes.| |
ACKNOWLEDGEMENTS |
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We thank the athletes who volunteered to participate in the study and Prof. E. M. Schneider, University of Ulm (Ulm, Germany) for helpful discussions regarding our manuscript.
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FOOTNOTES |
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This investigation was supported by a grant from the Bundesinstitut für Sportwissenschaft (Koeln, Germany, VF 0407/01/21/97).
Address for reprint requests and other correspondence: E. Fehrenbach, Abteilung Transfusionsmedizin, Eberhard-Karls-Universitaet Tuebingen, Otfried-Mueller-Str. 4/1, D-72076 Tuebingen, Germany (E-mail: elvira.fehrenbach{at}med.uni-tuebingen.de).
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. §1734 solely to indicate this fact.
Received 1 February 2000; accepted in final form 1 April 2000.
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TOP
ABSTRACT
INTRODUCTION
MATERIALS AND METHODS
RESULTS
DISCUSSION
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