Skip to main content

Platelets activation is associated with elevated plasma mitochondrial DNA during cardiopulmonary bypass



Mitochondrial DNA (mtDNA) was reported as a pro-inflammatory agent. In our previous study, elevation of plasma mtDNA was revealed after cardiac surgery with cardiopulmonary bypass (CPB). Platelets were activated during the cardiac surgery and recent study revealed its ability to release mtDNA. Our present study postulated that the elevated plasma mtDNA comes from activated platelets, which plays a critical role in post-CPB inflammatory responses.


Sixty-eight patients who underwent coronary artery bypass graft (CABG) with CPB were enrolled in our study. Blood samples were collected before induction of anaesthesia (T1), at the end of CPB (T2), 12 h post-CPB (T3), 24 h post-CPB (T4), 48 h post-CPB (T5) and 72 h post-CPB (T6). Blood samples were analyzed for the routine blood test and prepared for plasma isolation. MtDNA concentration was measured by rt-PCR, and TNF-α and IL-6 were examined by specific ELISA kits. Subgroup study was analyzed by activation levels of platelet. Basic information, mtDNA level, TNF-α level and IL-6 level were all carefully studied in each quartile.


Activation level of platelets increased and peaked at T2, which decreased gradually from T3 to T6 (P < 0.05). MtDNA increased after CPB, peaked at T3, and then backed from T4 to T6 (P < 0.05). Bivariate correlation between peak activation level of platelets and peak plasma mtDNA level showed a positive correlation between these two parameters (r = 0.683, P < 0.0001). Both TNF-α and IL-6 showed similar patterns as mtDNA, with an increase from T1 to T3 and a decrease from T4 to T6 (P < 0.05). Subgroup analysis further demonstrated that patients with higher activation levels of PLT had higher plasma mtDNA levels and inflammatory level (P < 0.05).


Our study revealed the dynamic changes of activation level of platelets and identified the interesting association between platelets activation and plasma mtDNA, suggesting a novel potential mechanism of activated platelets-induced post-CPB inflammatory responses.

Peer Review reports


Cardiac surgery under cardiopulmonary bypass (CPB) was firstly practiced in 1955 and reported by Kirklin JW, providing a new horizon for modern cardio-thoracic surgeries [1]. CPB can help bypass the circulation out of the heart and the lung, which offers a clear vision and stable condition for operation [2]. Although the low mortality for CPB is already analyzed, many harmful events were still reported. Myocardial ischemic/reperfusion injury (IRI) and abnormal status of circulation are two major causes for post-operative systemic inflammatory responses that take responsibilities for detrimental effects on the heart and distant organs [35]. Much endeavor has already been taken to decrease these negative effects. However, there is still lack of a sufficient way to control post-operative systemic inflammatory responses.

Mitochondria are considered to be organelles evolved both in saprophytic bacteria and endosymbiosis [6]. Mitochondrial DNA (mtDNA) consists of 16569 nucleotide bases which code 13 polypeptides [7]. Containing of CpG DNA repeats, mtDNA is widely studied as a pro-inflammatory agent. Many experiments report elevated plasma mtDNA after injuries, which is released into the circulation causing systemic inflammation [8, 9]. It is demonstrated that plasma mtDNA level can be used to improve risk prediction and predict mortality [10].

Activation of platelets is revealed during the cardiac surgery with CPB [11]. Dysfunction of platelets and severely decreased platelets are also reported after CPB [12]. Many studies are reported to use mean platelet volume/platelet count (MPV/platelet count) to represent the activation level of platelets [13]. It is demonstrated that activated platelets could release many pro-inflammatory cytokines causing systemic inflammatory responses [14]. Recently, Luc H. Boudreau, et al informed that activated platelets could release mtDNA into the circulation and promote inflammation through serving as substrates for bactericidal group IIA [15].

Our previous study has revealed the variation of plasma mtDNA level during and after cardiac surgery with CPB. In the present study, given the mtDNA releasing property of activated platelets, we postulated that activated platelets might, at least partially, take the responsibility for the elevated plasma mtDNA during the cardiac surgery with CPB. The present study aimed to explore whether platelets activation was associated with changes in levels of plasma mtDNA during CPB. Meanwhile, we also examined the relationship between platelet activation and inflammatory cytokines during CPB.


Study population

Sixty-eight patients requiring coronary artery bypass graft (CABG) with CPB were included consecutively in our study from January 2014 to January 2015, who were admitted to the Department of Cardiovascular Surgery, West China Hospital, Sichuan University. Medical history including endocarditis, diabetes, hypertension, any infectious diseases, chronic inflammatory diseases, hematologic disorders that affect platelet count or platelets function, autoimmune diseases, post-operative acute renal failure, low cardiac output syndrome were designed as the excluding criteria. Pre-operative laboratory tests and examinations were carefully arranged and all patients had normal functions of kidney, liver and lung. Informed consents were signed by every patient or their family members. Post-operative standard care in cardiac intensive unit (CICU) were scheduled as the routine element for all patients. This protocol was conducted following the Declaration of Helsinki and approved by the West China Hospital Ethics Committee (No. 2012 (150)).

Collection of blood samples

Blood samples were collected in two EDTA-coated blood collection tubes before induction of anaesthesia (T1), at the end of CPB (T2), 12 h post-CPB (T3), 24 h post-CPB (T4), 48 h post-CPB (T5) and 72 h post-CPB (T6). One blood collection tube was for the routine blood test immediately and results were reported by the Division of Clinical Hematology, West China Hospital, Sichuan University. The other tube was also immediately centrifuged at 1000 rpm/min for 15 min at 4 °C and the supernatant was transferred to a new tube as plasma without touching the pellet or the bottom of the tube. All plasma samples were rapidly stored in −80 °C freezer (Thermo, USA) and ready for the DNA isolation and ELISA assay. All procedures were conducted carefully to avoid contamination.

DNA isolation and rt-PCR assay

The whole plasma DNA was isolated from plasma using the DNeasy Blood and Tissue Kit (#69504, Qiagen) as our previous report [16]. Briefly, 50 μL plasma sample was added to 50 μL phosphate buffered saline (PBS) and then centrifuged at 16000 g for 15 min at 4 °C. 90 μL of supernatant were kept for the next procedures. The rest procedures were performed exactly according to the manufacture’s protocol. At the last step, 200 μL elution buffer was added to resolve the DNA.

Plasma mtDNA levels were measured by SYBR-green dye-based rt-PCR assay using a PRISM 7300 sequence detection system. The primer sequences detecting mtDNA were human NADH dehydrogenase 1 gene: forward CGAGCAGTAGCCCAAACAAT, reverse TGTGATAAGGGTGGAGAGGTT. Plasmid DNA with complementary DNA sequence for human mtDNA was obtained from ORIGENE (SC101172, USA). Concentration of plasma mtDNA were converted to copy number via a DNA copy number calculator (; University of Rhode Island Genomics and Sequencing Center). Plasmid DNA was diluted in 10-fold serial dilutions and used as the standard curve. Every samples were studied three times for quality control.

All samples were measured with standards at the same time. Plasma mtDNA levels were shown in copies per microliter of plasma (copies/μL) according to the following formula:

$$ \mathrm{c} = \mathrm{Q}\ *\ {\mathrm{V}}_{\mathrm{DNA}}/{\mathrm{V}}_{\mathrm{PCR}}*\ 1/{\mathrm{V}}_{\mathrm{ext}} $$

where c is the concentration of plasma mtDNA (copies/μL); Q means quantity of DNA measured by rt-PCR; VDNA means the total volume of plasma DNA solution obtained from extraction, 200 μL in this study; VPCR means the volume of plasma DNA solution for rt-PCR, 1 μL in this study; Vext means the volume of plasma used for extraction, 50 μL in this study.

Plasma TNF-α and IL-6 measurement

Plasma TNF-α and IL-6 was measured by the enzyme-linked immunosorbent assay (ELISA) kits, specifically designed for human TNF-α and IL-6, respectively (Solarbio, China). All procedures were carried out following the standard protocols (included in ELISA kits). Three duplicated samples were set and all samples were measured with serial diluted standards at the same time. Spectrophotometry (VARIOSKAN, Thermo, USA) was used to detect the intensity of the transmitted light. Data was expressed in picogram per mL (pg/mL).

Statistical analysis

All descriptive data was shown as mean ± standard error of the mean (SEM) and analyzed with SPSS statistical software version 20.0 for Windows (SPSS, Inc. Chicago, IL, USA). All descriptive data was near-normal by SPSS analysis. Multiple comparisons were analyzed by the one-way ANOVA followed by Bonferroni’s test. The Pearson correlation coefficient test was performed to analyze the relationship between MPV/platelet count and plasma mtDNA. Data (platelet count, mtDNA, TNF-α, IL-6) collected after T1 was corrected by hematocrit (Hct) at T1 due to the hemodilution during cardiac surgery (Datacorrected = Datacollection × HctT1/HctTx). P < 0.05 was considered as statistically significant.


Baseline information

Basic characteristics, surgical information and laboratory results of all patients were presented in Table 1. All sixty-eight patients were successfully performed CABG with CPB. No patient died or needed a second surgery during the hospitalization. The average age and BMI were (47.5 ± 15.2) years old and (24.1 ± 3.5). During surgery, the average time of aortic cross-clamping and total CPB were (64.3 ± 21.7) min and (96 ± 29.1) min, respectively. On the first day admission, basic laboratory data such as serum creatinine, total cholesterol (TC), high density lipoprotein (HDL), low density lipoprotein (LDL), triglycerides (TG), glucose, red blood cell count (RBC), white blood cell count (WBC), platelet count, MPV, hemoglobin (Hb) and Hct was collected and represented.

Table 1 Baseline information

Dynamic monitoring the activation of platelets

MPV/platelet count ratio was used to represent the activation level of platelets during the cardiac surgery. Through serial six blood samples for each patient, dynamic changes of activation level of platelets were monitored during the cardiac surgery with CPB. As shown in Fig. 1, platelet count, MPV and MPV/platelet count ratio were presented. Compared with T1, platelet count significantly decreased and touched the bottom at T2 (P < 0.05) following a gradually increasing back to the baseline level from T3 to T6. On the contrary, MPV increased significantly and reached the highest level at T2 comparing with T1 (P < 0.05), which dropped back to normal gradually. Therefore, MPV/platelet count climbed to the peak at T2 and decreased gradually (P < 0.05). Our data demonstrated that platelets were activated during the cardiac surgery with CPB and the highest activation level of platelets occurred at the end of CPB.

Fig. 1

Changes of perioperative platelets activation level. Platelets count decreased significantly at the end of CPB (T2) and increased from T3 to T6 (P < 0.05). Mean platelet volume (MPV) increased at T2 and then back to normal gradually (P < 0.05). MPV/platelet count increased significantly at T2 and decreased from T3 to T6 (P < 0.05). *P < 0.05 vs. T1. T1: before induction of anaesthesia; T2: at the end of CPB; T3: 12 h post-CPB; T4: 24 h post-CPB; T5: 48 h post-CPB; T6: 72 h post-CPB. Units of left y axis (platelet count): ×109 per litre; Units of left y axis (MPV): femtoliter (fl)

Plasma mtDNA changes and its correlation with peak MPV/platelet count

Plasma samples were used to examine plasma mtDNA levels by using rt-PCR technique (Data was shown in Fig. 2a). As presented, changes of plasma mtDNA was similar to MPV/platelet count, which increased significantly after T1 and decreased gradually from T4 to T6 (P < 0.05). However, the highest point happened at T3 for plasma mtDNA.

Fig. 2

a Variation of plasma mtDNA during the cardiac surgery with CPB and the correlation between peak activation level of platelets and peak plasma mtDNA level. Plasma mtDNA level increased significantly and peaked at T3, which decreased slowly from T3 to T6 (P < 0.05). b Bivariate correlation study showed a positive correlation between peak activation level of platelets and peak plasma mtDNA level (r = 0.683, P < 0.0001). *P < 0.05 vs. T1. Units of y axis: copies per microliter (copies/μL)

To illustrate the relationship between platelets activation and plasma mtDNA, bivariate correlation analysis was used. Since we excluded other possible complications that might disturb our results, the peak MPV/platelet count and peak plasma mtDNA were used to stand for platelets activation level and mtDNA releasing level, respectively, during the cardiac surgery with CPB. As shown in Fig. 2b, positive correlation was analyzed between these two parameters (r = 0.683, P < 0.001). These data demonstrated a close relationship between platelets activation and plasma mtDNA.

Levels of TNF-α and IL-6

Plasma TNF-α and IL-6 levels were measured by ELISA kits in all plasma samples. Data was presented in Fig. 3. Both TNF-α and IL-6 increased since T2 and got the highest level at T3, followed by a gradual decreasing from T4 to T6 (P < 0.05). Consistence with previous studies, our study confirmed dynamic changes of perioperative plasma TNF-α and IL-6 levels.

Fig. 3

Merged curve of perioperative inflammatory cytokines in the cardiac surgery with CPB. Both TNF-α and IL-6 were elevated significantly after CPB (P < 0.05). Levels of TNF-α and IL-6 peaked at T3 (P < 0.05). *P < 0.05 vs. respective T1. Units of y axis: picogram per milliliter (pg/mL)

Subgroup analysis

According to our study, activation level of platelets peaked at the end of CPB (T2) and the mean value of MPV/platelet count was 0.12 ± 0.019 (0.069–0.162). Distribution of study population was shown in Fig. 4. Subgroups were defined as follow: Quartile 1, MPV/platelet count <0.09 (N = 14); Quartile 2, MPV/platelet count = 0.09–0.11 (N = 17); Quartile 3, MPV/platelet count = 0.11–0.13 (N = 22); Quartile 4, MPV/platelet count >0.13 (N = 15).

Fig. 4

Distribution of study population according to the activation level of platelets

We analyzed the baseline information for each quartile, shown in Table 2. Average age, BMI, time of aortic cross-clamping, total CPB, serum creatinine, TC, HDL, LDL, TG, glucose, RBC, WBC, Hb and Hct were carefully calculated and showed no significance between four quartiles. Meanwhile, plasma mtDNA level, TNF-α and IL-6 at 12 h post-CPB (T3) were also included to compare among four quartiles. Intriguingly, significant differences were observed among four quartiles. In general, patients in the higher MPV/platelet count quartiles had higher level of plasma mtDNA, TNF-α and IL-6 (P < 0.05). The present study indicated that higher levels of plasma mtDNA, TNF-α and IL-6 were related to the higher MPV/platelet count quartiles, further implying that mtDNA might come from activated PLT and play a pro-inflammatory role.

Table 2 Subgroup analysis


In our present study, we first dynamically monitored the activation level of platelets by analyzing MPV/platelet count ratio during the cardiac surgery with CPB, showing that platelets activation level peaked at the end of CPB. In addition, like our previous study, we revealed the variation of plasma mtDNA and inflammatory cytokines (TNF-α and IL-6). To study the possible source of plasma mtDNA, bivariate correlation analysis was used and demonstrated that the peak MPV/platelet count ratio was positively correlated with the peak plasma mtDNA level. Subgroup analysis also suggested that patients with CPB with higher peak MPV/platelet count ratio had higher post-CPB plasma mtDNA level and higher systemic inflammatory level.

During cardiac surgery with CPB, the blood flows out of the vessels and goes through the circuits. A large number of studies demonstrated that exposure of blood to the bypass circuit surface initiated systemic inflammatory responses, taking responsibility for post-CPB inflammation and organ dysfunction [17]. It is well known that the activation of platelets during the CPB could cause post-CPB inflammatory responses. Additionally, some studies revealed that activated platelets played its role in inflammation via expression of P-selectin and CD40 ligand [18, 19]. Recently, Procter NE, et al identified that the hyper-aggregability of platelets could cause inflammation through MPO-related pathway in patients with atrial fibrillation [20]. Therefore, anti-coagulation strategy was widely used in the cardiac surgery with CPB and heparin-coated circuits were also applied to abate the inflammation and coagulation [21]. In our study, we illustrated the dynamic changes of platelets activation during the cardiac surgery with CPB. Unsurprisingly, rapid activation of platelets was shown and activation level peaked at the end of CPB. Meanwhile, post-CPB inflammatory level was also shown in our study and the peak level of inflammatory responses occurred at 12 h post-CPB, which is 12 h later than the peak point of platelets activation. Given the well-known pro-inflammatory properties of activated platelets, our data suggested that activation of platelets might promote post-CPB inflammatory responses.

Although many studies focused on the mechanism between activated platelets and inflammation, it was still not fully understood. In our previous study, a tight and strong relationship between post-CPB plasma mtDNA level and plasma inflammatory cytokines was revealed. Therefore, elevated plasma mtDNA was regarded as a pro-inflammatory agent during the cardiac surgery with CPB and promoted post-CPB inflammatory responses. A study conducted by Luc H. Boudreau, et al suggested that activated platelets can release mitochondria and mtDNA. Transfused patients and in vitro platelets activation study were used to evaluate the mtDNA changes [15]. Platelets, as small discoid anucleate cell fragment from megakaryocytes, contained cytoplasmic organelles, including mitochondria. After the activation of platelets, intracellular components were released via the cytoplasmic granules formation and the fusion with the plasma membrane [22]. Given that the perioperative variation of plasma mtDNA level we studied, it is possible that most of post-CPB plasma mtDNA were from activated platelets. In our study, we found the peak platelets activation time is T2 and peak mtDNA level occurred at T3, which mean that the mtDNA elevation came after the platelets activation. Bivariate correlation analysis was applied to study the correlation between peak platelets activation level and peak plasma mtDNA level. Since the time gap and positive correlation, our results suggested that activated platelets might be the source of plasma mtDNA during the cardiac surgery with CPB.

MtDNA has been widely studied recently, which could cause systemic inflammation when it was released into the circulation [23]. Plasma mtDNA was captured into leukocytes and acts as bacteria to cause inflammatory responses [24]. Studies found that plasma mtDNA level can represent the invasiveness and complexation of surgeries [25]. In vivo study revealed that injection of mtDNA can cause severe systemic inflammatory responses and multiple organ dysfunction [23]. Consistent with our previous study, mtDNA level after cardiac surgery was correlated with inflammatory response level. And in the present study, we concluded that activated platelets may take responsibilities for the elevated mtDNA level. However, many other factors are also considered to account for elevated mtDNA. Many studies reported the myocardial ischemia/reperfusion injuries after cardiac surgery with CPB [26, 27]. During the ischemia/reperfusion injury, myocardial tissue damage may cause mtDNA releases. Also, the damage of surgery itself to the heart can cause tissue damage and mtDNA release.

In order to further study the relationship between activated platelets and plasma mtDNA, we conducted the subgroup analysis. Four quartiles according to platelets activation levels were set. Unsurprisingly, patients with higher platelets activation level presented higher level of plasma mtDNA and suffered higher level of post-CPB inflammation. Levels of TNF-α and IL-6 represented the severity of post-CPB inflammatory responses [28]. Post-CPB inflammation might cause a delay of the recovery and deteriorate the hospital outcomes [29]. Above all, our data revealed the tight association between platelets activation and elevated plasma mtDNA level, suggesting that activated platelets might cause post-CPB inflammation through releasing mtDNA.

Although we got some excellent results, our study still has many limitations. Our study only enrolled sixty-eight patients undergoing CABG with CPB. To further study the relationships among platelets, mtDNA and inflammatory responses, a large-scale study is needed. Additionally, more specific and statistical grouping and subgrouping setting should be designed. Moreover, we still need further experiments or clinic study to achieve the direct evidences to prove our speculation. Finally, our study can only provide a preliminary result about the role of mtDNA in platelets-mediated post-CPB inflammatory responses, but raise a clinical foundation for further relative studies.


Our study demonstrated the positive correlation between platelets activation and peak plasma mtDNA level during the cardiac surgery with CPB, which explains the possible source of abundant plasma mtDNA after CPB. Therefore, in combination with our previous study, we raised a novel potential theory that mtDNA might act as a mediator between platelets and inflammation after cardiac surgery with CPB and platelets might act as a valuable target to modify the inflammation.


  1. 1.

    Kirklin JW, Dushane JW, Patrick RT, Donald DE, Hetzel PS, Harshbarger HG, Wood EH. Intracardiac surgery with the aid of a mechanical pump-oxygenator system (gibbon type): Report of eight cases. Proc Staff Meet Mayo Clin. 1955;30:201–6.

    CAS  PubMed  Google Scholar 

  2. 2.

    Zhang Z, Wu Y, Zhao Y, Xiao X, Liu J, Zhou X. Dynamic changes in hmgb1 levels correlate with inflammatory responses during cardiopulmonary bypass. Experimental and therapeutic medicine. 2013;5:1523–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. 3.

    Banz Y, Rieben R, Zobrist C, Meier P, Shaw S, Lanz J, Carrel T, Berdat P. Addition of dextran sulfate to blood cardioplegia attenuates reperfusion injury in a porcine model of cardiopulmonary bypass. Eur J Cardiothorac Surg. 2008;34:653–60.

    Article  PubMed  Google Scholar 

  4. 4.

    Bel A, Borik W, Davidson S, et al. Inhibition of factor IXa by the pegnivacogin system during cardiopulmonary bypass: a potential substitute for heparin. A study in baboons [J]. Eur J Cardiothorac Surg. 2016;49(2):682–9.

  5. 5.

    Chuah C, Kirkbride R, Alston R, Irons J. Hydrogen ion concentration and coronary artery bypass graft surgery with and without cardiopulmonary bypass. Eur J Cardiothorac Surg. 2013;8:184.

    Article  Google Scholar 

  6. 6.

    Zhang Q, Raoof M, Chen Y, Sumi Y, Sursal T, Junger W, Brohi K, Itagaki K, Hauser CJ. Circulating mitochondrial damps cause inflammatory responses to injury. Nature. 2010;464:104–7.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  7. 7.

    Wallace DC. Mitochondrial DNA in aging and disease. Sci Am. 1997;277:40–7.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Itagaki K, Kaczmarek E, Lee YT, Tang IT, Isal B, Adibnia Y, Sandler N, Grimm MJ, Segal BH, Otterbein LE, Hauser CJ. Mitochondrial DNA released by trauma induces neutrophil extracellular traps. PLoS One. 2015;10:e0120549.

    Article  PubMed  PubMed Central  Google Scholar 

  9. 9.

    Puskarich MA, Shapiro NI, Trzeciak S, Kline JA, Jones AE. Plasma levels of mitochondrial DNA in patients presenting to the emergency department with sepsis. Shock. 2012;38:337–40.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  10. 10.

    Nakahira K, Kyung SY, Rogers AJ, Gazourian L, Youn S, Massaro AF, Quintana C, Osorio JC, Wang Z, Zhao Y, Lawler LA, Christie JD, Meyer NJ, Mc Causland FR, Waikar SS, Waxman AB, Chung RT, Bueno R, Rosas IO, Fredenburgh LE, Baron RM, Christiani DC, Hunninghake GM, Choi AM. Circulating mitochondrial DNA in patients in the icu as a marker of mortality: Derivation and validation. PLoS Med. 2013;10:e1001577. discussion e1001577.

    Article  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Tabata S, Yamaguchi S, Nagamine H, Tomita S, Arai S, Takemura H, Watanabe G. Efficacy of fk633, an ultra-short acting glycoprotein iib/iiia antagonist on platelet preservation during and after cardiopulmonary bypass. Eur J Cardiothorac Surg. 2004;26:289–93.

    Article  PubMed  Google Scholar 

  12. 12.

    Sniecinski RM, Chandler WL. Activation of the hemostatic system during cardiopulmonary bypass. Anesth Analg. 2011;113:1319–33.

    Article  PubMed  Google Scholar 

  13. 13.

    Cho SY, Jeon YL, Kim W, Kim WS, Lee HJ, Lee WI, Park TS. Mean platelet volume and mean platelet volume/platelet count ratio in infective endocarditis. Platelets. 2014;25:559–61.

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Varon D, Shai E. Platelets and their microparticles as key players in pathophysiological responses. J Thromb Haemost. 2015;13 Suppl 1:S40–46.

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Boudreau LH, Duchez AC, Cloutier N, Soulet D, Martin N, Bollinger J, Pare A, Rousseau M, Naika GS, Levesque T, Laflamme C, Marcoux G, Lambeau G, Farndale RW, Pouliot M, Hamzeh-Cognasse H, Cognasse F, Garraud O, Nigrovic PA, Guderley H, Lacroix S, Thibault L, Semple JW, Gelb MH, Boilard E. Platelets release mitochondria serving as substrate for bactericidal group iia-secreted phospholipase a2 to promote inflammation. Blood. 2014;124:2173–83.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  16. 16.

    Qin C, Liu R, Gu J, Li Y, Qian H, Shi Y, Meng W. Variation of perioperative plasma mitochondrial DNA correlate with peak inflammatory cytokines caused by cardiac surgery with cardiopulmonary bypass. J Cardiothorac Surg. 2015;10:85.

    Article  PubMed  PubMed Central  Google Scholar 

  17. 17.

    Ziyaeifard M, Alizadehasl A, Massoumi G. Modified ultrafiltration during cardiopulmonary bypass and postoperative course of pediatric cardiac surgery. Research in cardiovascular medicine. 2014;3:e17830.

    PubMed  PubMed Central  Google Scholar 

  18. 18.

    Henn V, Slupsky JR, Grafe M, Anagnostopoulos I, Forster R, Muller-Berghaus G, Kroczek RA. Cd40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells. Nature. 1998;391:591–4.

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Goddard A, Leisewitz AL, Kristensen AT, Schoeman JP. Platelet activation and platelet-leukocyte interaction in dogs naturally infected with babesia rossi. Vet J. 2015;205(3):387–92.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Procter NEK, Ball J, Ngo DTM, et al. Platelet hyperaggregability in patients with atrial fibrillation [J]. Herz. 2015:1–16.

  21. 21.

    Teligui L, Dalmayrac E, Mabilleau G, Macchi L, Godon A, Corbeau JJ, Denomme AS, Bouquet E, Boer C, Baufreton C. An ex vivo evaluation of blood coagulation and thromboresistance of two extracorporeal circuit coatings with reduced and full heparin dose. Interact Cardiovasc Thorac Surg. 2014;18:763–9.

    Article  PubMed  Google Scholar 

  22. 22.

    Koseoglu S, Flaumenhaft R. Advances in platelet granule biology. Curr Opin Hematol. 2013;20:464–71.

    Article  PubMed  Google Scholar 

  23. 23.

    Gan L, Chen X, Sun T, Li Q, Zhang R, Zhang J, Zhong J. Significance of serum mtdna concentration in lung injury induced by hip fracture. Shock. 2015;44:52–7.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Walko 3rd TD, Bola RA, Hong JD, Au AK, Bell MJ, Kochanek PM, Clark RS, Aneja RK. Cerebrospinal fluid mitochondrial DNA: A novel damp in pediatric traumatic brain injury. Shock. 2014;41:499–503.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  25. 25.

    McIlroy DJ, Bigland M, White AE, Hardy BM, Lott N, Smith DW, Balogh ZJ. Cell necrosis-independent sustained mitochondrial and nuclear DNA release following trauma surgery. The journal of trauma and acute care surgery. 2015;78:282–8.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Minamino T. Cardioprotection from ischemia/reperfusion injury: Basic and translational research. Circ J. 2012;76:1074–82.

    CAS  Article  PubMed  Google Scholar 

  27. 27.

    Hausenloy DJ, Yellon DM. Myocardial ischemia-reperfusion injury: A neglected therapeutic target. J Clin Invest. 2013;123:92–100.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  28. 28.

    Mei YQ, Ji Q, Liu H, Wang X, Feng J, Long C, Cheng B, Xing Y, Li J, Hu D. Study on the relationship of apache iii and levels of cytokines in patients with systemic inflammatory response syndrome after coronary artery bypass grafting. Biol Pharm Bull. 2007;30:410–4.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Kourliouros A, Karastergiou K, Nowell J, Gukop P, Tavakkoli Hosseini M, Valencia O, Mohamed Ali V, Jahangiri M. Protective effect of epicardial adiponectin on atrial fibrillation following cardiac surgery. Eur J Cardiothorac Surg. 2011;39:228–32.

    Article  PubMed  Google Scholar 

Download references


This study was financially supported by the National Natural Science Foundation of China (No. 8150036, No. 81370413, No. 81500213).

Authors’ contributions

CQ and JG carried out the molecular studies and drafted the manuscript. JH and XF performed the statistical analyses. HQ and YL participated in the sample collection. RL participated in coordination and helped to draft the manuscript. WM participated in the design of the study and performed the statistical analysis. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Author information



Corresponding author

Correspondence to Wei Meng.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Qin, C., Gu, J., Hu, J. et al. Platelets activation is associated with elevated plasma mitochondrial DNA during cardiopulmonary bypass. J Cardiothorac Surg 11, 90 (2016).

Download citation


  • Platelets
  • Mitochondrial DNA
  • Inflammation
  • Cardiopulmonary bypass