1. Introduction
Mitochondria are key components in cellular metabolism, cell growth, apoptosis, calcium homeostasis, redox status, etc., and their dysfunction has been implicated as a therapeutic target for various diseases [
1]. Mitochondrial transplantation has been first proposed to be useful for the treatment of ischemia-reperfusion injury of the heart, and it shows promising clinical benefits regarding neonatal congenital heart diseases [
2,
3].
Mitochondrial transplantation enhances oxygen consumption, ATP synthesis, cell viability and post-infarct cardiac function [
3]. Given these interesting findings, many diseases are being investigated as candidates for mitochondrial transplantation in both preclinical and clinical studies [
4]. In sepsis, mitochondrial damage is critical, and therapeutic drugs might be used to enhance mitochondrial function. However, in cases of irreversible damage, mitochondrial transplantation could be a novel strategy [
5]. We previously showed that mitochondrial transplantation could have immune modulation effects in the sepsis model [
6]. Mitochondria are known to be different in terms of number, size, shape, distribution, and feature from cell to cell [
7]. Therefore, the identification of the best mitochondrial donor cell is a very important issue in mitochondrial transplantation [
8]. Skeletal muscle and MSCs have been suggested as an appropriate candidate for mitochondrial isolation [
7]. Skeletal muscle has plenty of mitochondria, so it could be a good source cell for mitochondrial transplantation. MSCs are present in a quiescent state and appear to be primarily glycolytic. However, when transferred to the nutrient-rich artificial culture environment, MSCs become dependent on oxidative phosphorylation [
9]. MSC has advantages for cell therapy or mitochondrial transplantation: viability and regenerative capacity after preservation at −80 °C; simplicity of isolation and cryopreservation; rapid replication; and minimal immunoreactivity [
10]. Hepatocytes are enriched with mitochondria that comprise 13–20% of the liver volume [
11].
With this in mind, we hypothesized that the effects of transplanting mitochondria would vary depending on the cell type from which they were isolated. To test this hypothesis, we used both in vivo and in vitro sepsis models. We isolated mitochondria from three different cell lines: L6 muscle cell line, clone 9 hepatocyte cell line, and MSC, mesenchymal stem cell. We examined the immunomodulatory effects and survival of mitochondrial transplantation using different cell types for mitochondrial isolation (
Figure 1).
3. Discussion
This study is the first to demonstrate the effects of mitochondrial transplantation on sepsis models could vary depending on the cell type, from which mitochondria were isolated. Additionally, we showed that the oxidative phosphorylation function (oxygen consumption rate) of mitochondria differs depending on their origin cell. L6-mitochondria exhibited superior mitochondria function when transplanted into in vitro sepsis model in terms of oxidative phosphorylation. Furthermore, L6-mitochondrial transplantation displayed a more pronounced survival effect in the in vivo sepsis model, compared to MSC or clone 9 cell.
Mitochondria are found in all mammalian cells except in red blood cells [
12]. Classically, the function of mitochondria was considered to produce energy factories. However, it has been known that mitochondria have multiple important functions such as calcium homeostasis, redox status, control of apoptosis, cell proliferation, or immune modulation effect [
13]. Mitochondrial dysfunction was considered the main pathophysiology in various important diseases [
1,
14]. With this background, mitochondrial transplantation has been widely investigated as a therapeutic strategy for many mitochondrial dysfunction [
12,
15]. To perform mitochondria transplantation, it is necessary to isolate healthy mitochondria from cells, which have different characteristics in terms of number, size, shape, distribution, and functions [
7]. Consequently, the effects of mitochondria transplantation might be different depending on the specific cell types from which the mitochondria are isolated.
Previously, we demonstrated the immune modulation effects of mitochondria transplantation on both in vivo and in vitro sepsis models using L6 cells for mitochondria isolation. In the present study, we utilized different healthy cells to isolate the mitochondria, and observed that L6-mitochondria exhibited superior effects when transplanted on the in vitro sepsis model in terms of mitochondrial oxidative phosphorylation. These findings were consistent in the fecal slurry sepsis animal model, with a higher survival rate.
The effects of mitochondrial transplantation were investigated both in terms of oxidative phosphorylation and immune modulation. We hypothesized that mitochondrial transplantation would enhance mitochondrial oxidative phosphorylation, which in turn would promote immune modulation. However, contrary to our expectations, these effects were not correlated. L6-mitochondrial transplantation exhibited a significantly greater enhancement of oxidative phosphorylation compared to clone 9- or MSC-mitochondrial transplantation, but there were no significant differences in immune modulation effects. Interestingly, L6-mitochondrial transplantation resulted in a higher survival rate compared to clone 9- or MSC-mitochondrial transplantation. We did not investigate the exact mechanism by which mitochondrial transplantation influences oxidative phosphorylation. It might simply supply oxidative phosphorylation enzymes although other mechanisms may also be involved. Further investigation is needed to explore these possibilities.
Mitochondria transplantation has been studied in various diseases, especially ischemia-reperfusion injury [
7,
16]. Currently, it is unknown whether the transplantation of L6 mitochondira would have better effects on ischemia-reperfusion injury. Further experiments are needed to discover this.
This study has several limitations. First, we only tested three cell types for mitochondrial isolation. More cell types are needed to determine the best candidate cells for mitochondria isolation. Second, the specific mode of action of mitochondrial transplantation was not elucidated. The mechanism might be complex considering the various processes, in which mitochondria are involved (e.g., energy production, redox status, apoptosis, calcium modulation), and one specific mechanism might not be responsible for the whole beneficial effects. Despite these limitations, this study is the first to investigate the effects of mitochondria transplantation on sepsis depending on the cell types from which they are isolated.
4. Materials and Methods
4.1. Mitochondria Isolation from Different Cell Types and Mitochondrial Transplantation
Mitochondrial isolation methods have been previously described [
6]. We purified mitochondria from L6 (ATCC; CRL-1458, Manassas, VA, USA), clone 9 (ATCC; CRL-1439, Manassas, VA, USA), and umbilical cord mesenchymal stem cells (UC-MSCs; IRB No. 201806-BR-029-03) by differential centrifugation, which yielded mitochondrial extract as determined by bicinchoninic acid (BCA) assay.
L6 and clone 9 cells were homogenized in SHE buffer (0.25 M sucrose, 20 mM HEPES, 2 mM EGTA, 10 mM KCl, 1.5 mM MgCl2, 0.1% defatted bovine serum albumin [BSA], protease inhibitor, pH 7.4) and then centrifuged at 1500× g for 5 min to remove cells and cell debris. After centrifugation, the mitochondria-containing supernatant was subsequently centrifuged at 20,000× g for 10 min. UC-MSCs were homogenized in SHE buffers and centrifuged at 1100× g for 3 min. The supernatant was centrifuged at 12,000× g for 15 min to obtain a mitochondrial pellet and then resuspended the pellet in SHE buffers without BSA. Finally, the mitochondrial suspension was centrifuged at 20,000× g for 10 min. All centrifugation steps are performed at 4 °C.
The mitochondrial suspension (in 10 µg/10 μL of PBS) and LPS were added slowly to each tube of recipient cells (1 × 105) suspended in 500 μL of RPMI 1640 supplemented with 10% fetal bovine serum [FBS], 1% penicillin-streptomycin [P/S]. After cell seeding into 48-well plates, we centrifuged it at 1500× g for 5 min and then incubated at 37 °C and 5% CO2.
4.2. ATP Assay
ATP content and ATP synthesis in isolated mitochondria from L6, clone 9, and MSC were assessed using a CellTiter-Glo Luminescent Cell Viability Assay (Promega, Madison, WI, USA). To detect ATP content, 10 μg of isolated mitochondria was incubated with CellTiter-Glo reagent at room temperature for 10 min. To measure ATP synthesis, 5 mM of ADP solution was added to 10 μg of isolated mitochondria and then incubated at 37 °C for 45 min. After incubation, the samples were incubated with CellTiter-Glo reagent at room temperature for 10 min. All experiments were performed protected from light. The luminoscence was measured on a luminometer (BioTex, Winooski, VT, USA).
4.3. Stimulation of THP-1 with LPS
The hyperinflammation model was induced by treating THP-1 cells (ATCC, Manassas, VA, USA) with 50 ng/mL lipopolysaccharide (LPS) for 4 h. To estimate the anti-inflammatory effect of mitochondrial transplantation, THP-1 cells were co-incubated with LPS and isolated mitochondria in each cell type. The endotoxin tolerance model was stimulated with 10 ng/mL LPS for 4 h as the first stimulus, followed by resting in a fresh medium without LPS for 16 h. Cells were re-stimulated with 10 ng/mL LPS for another 4 h. To assess the immune-modulation effect of mitochondrial transplantation, cells were treated with purified mitochondria during each LPS exposure. After incubation, cell culture supernatants were collected, and TNF-alpha secretion was measured using enzyme-linked immunosorbent assay (ELISA).
4.4. Measurement of Oxygen Consumption Rate
After being cultured for 24 h with LPS and isolated mitochondria, OCR was measured in THP-1 cells using a Seahorse XF analyzer and a Seahorse XF Cell Mito Stress Test kit (Agilent, Santa Clara, CA, USA). THP-1 cells were suspended in Seahorse XF RPMI medium (10 mM glucose, 1 mM sodium pyruvate, and 2 mM L-glutamine) and seeded in Cell-Tak coated XFe96 microplates (1 × 105 cells/well). Cells were then equilibrated in a non-CO
2 incubator for 1 h at 37 °C. The mitochondrial inhibitors (1.5 µM oligomycin, 2 µM FCCP, and 0.5 µM rotenone and antimycin) were serially injected to each well during the assay. It begins with measuring the base level of OCR, as the complex III inhibitor oligomycin injects, the OCR is rapidly decreased. This will be reversed by the injection of FCCP, an uncoupling agent that can dissipate the proton gradient and maximize the OCR. Finally, followed by the injection of Rotenone/antimycin A, the OCR decreases again. Parameters calculated in the form of a bar chart include ATP-linked respiration, proton leak, basal respiration, maximal respiration, and spare respiratory capacity. Basal respiration shows the energetic demand of cells under basal conditions, the oxygen consumption of basal respiration is used to meet ATP synthesis and results in mitochondrial proton leak. ATP-linked respiration is reflected by the decrease in OCR following the injection of the ATP synthase inhibitor oligomycin, which is the portion of basal respiration. The remaining basal respiration not coupled to ATP synthesis after oligomycin injection represents the proton leak, which can be a sign of mitochondrial damage. Maximal respiration represents the maximum capacity that the electron respiratory chain can achieve. The maximal oxygen consumption rate is measured by the injection of the uncoupler FCCP. Spare respiration is the difference between maximal and basal respiration, which reflects the capability of the cells to respond to changes in energetic demand and indicates the fitness of the cells. Non-mitochondrial respiration is oxygen consumption due to cellular enzymes other than mitochondria after the injection of rotenone and antimycin A [
17]. The OCR data were analyzed using the Seahorse Wave 2.6.1 Software.
4.5. In Vivo Rat Sepsis Model
This study was approved by the Institutional Animal Care and Use Committee of the authors’ institute (IACUC-220052), in accordance with the National Institutes of Health Guidelines. This study was carried out in compliance with the ARRIVE guidelines. Male Sprague-Dawley rats weighing 270–330 g were used. The rats were housed in a controlled environment (Room temperature 20~24 °C, humidity 40~60%) with access to standard food and water ad libitum for 7 days before the experiment.
We used a body weight-adjusted polymicrobial sepsis model according to a previous study [
18]. In brief, we used inhalation anesthesia with isoflurane for the short term and then injected intramuscular Zoletil (50 mg/kg) and Xylazine (10 mg/kg) before experiments. Feces were collected from donor rats. A midline laparotomy was performed, and the cecum was extruded. A 0.5 cm incision was made in the antimesenteric surface of the cecum and it was squeezed to expel feces. The collected feces were weighed and diluted with 5% dextrose saline at a ratio of 1:3. This fecal slurry was vortexed to make a homogeneous suspension before administration into the intraperitoneal cavity. In sepsis induction, rats were anesthetized as above, and 0.5 cm midline laparotomy was performed, and fecal slurry was administered into the peritoneal cavity. The volume of fecal slurry given to each animal was adjusted on the body weight of the recipient rat. We administered subcutaneous fluid resuscitation (30 mL/kg 5% dextrose saline) and imipenem was injected subcutaneously at a dose of 25 mg/kg twice daily for 2 days. We did not use painkillers. Thereafter, the rats were randomly assigned to 4 groups, mitochondrial transplantation (L6, clone 9, MSC) and control groups (
Figure 2A). Randomization was done by a research assistant, who was not performing the main procedure. The researcher who was performing the main procedures was blind to the allocated groups. The body weight of rats could be a confounder, so we randomized it with the body weight-stratified method. We did not think other confounders could affect the results with this study design, so it was not controlled.
Mitochondria or DPBS were administered 1 h after sepsis induction at a dose of 200 µg via the tail vein. Survival was monitored every 12 h for 14 days. During the observation period, an employee of the animal research center monitored animals twice per day, and if the animal seemed close to death, they notified the research team, who made a decision for euthanasia.
4.6. Quantification of Cytokines
The levels of the cytokines TNF-α (ab181421, Abcam, Waltham, MA, USA) in THP-1 cell homogenates were measured using ELISA kits according to the manufacturer’s instructions. The optical density at 450 nm was detected by a VersaMax microplate reader (SoftMax Pro 7.1 software, Molecular Devices, San Jose, CA, USA).
4.7. Serum Alanine Aminotransferase (ALT) and Creatinine Concentration in Plasma
The ALT and creatinine levels in the plasma sample were determined by an automated chemistry analyzer (Beckman Coulter, Brea, CA, USA) [
19].
4.8. Arterial Blood Gas Analysis
Arterial blood samples were analyzed using an ABL 90 blood gas analyzer (radiometer, Copenhagen, Denmark). Blood was drawn into a syringe containing heparin and analyzed within 10 min or cooled immediately [
19].
4.9. Statistical Analysis
Data were expressed as mean ± standard deviation (SD). The normality for the distribution of variables was verified by the Shapiro–Wilk test. A One-way ANOVA with Bonferroni post hoc tests was used to compare means in the normally distributed data. If the distributions are not normal, the data were analyzed using the Kruskal–Wallis test. Survival probabilities were calculated using the Kaplan–Meier method. All p-value < 0.05 was considered significant. Statistical analysis was performed using EZR software, version 1.54 (Saitama Medical Center, Jichi Medical University, Saitama, Japan).