Exogenous Mitochondrial Transfer in Differentiating Brown Adipocytes and AGPAT2-Deficient Preadipocytes

摘要

Exogenous mitochondria of human and murine origin can be internalized by differentiating preadipocytes and tracked throughout adipogenic differentiation using imaging and genetic tools. While these mitochondria physically interact with the endogenous mitochondrial network, they do not increase the expression of markers associated with mature brown adipocytes.

摘要

Mitochondria are key signaling hubs; however, whether mitochondrial mass expansion is mechanistically required for differentiation remains an open question. AGPAT2 catalyzes the conversion of lysophosphatidic acid into phosphatidic acid, and its deficiency leads to adipose tissue deficiency and impaired adipogenesis associated with reduced mitochondrial mass. The impact of mitochondrial mass expansion on adipogenesis was assessed by transferring exogenous mitochondria into differentiating brown adipocytes. Whether mitochondrial transfer could rescue the impaired adipogenesis of AGPAT2-deficient cells was also investigated. Human and murine mitochondria were successfully transferred and incorporated into the endogenous mitochondrial network of differentiating mouse preadipocytes and persisted throughout brown adipogenesis. Adipogenic differentiation was required for the retention of transferred mitochondria. Mitochondrial transfer did not modify the expression of molecular markers of mature brown adipocytes or lipid droplet content, although it affected the relative distribution of lipid droplet size in a species-dependent manner. In Agpat2^-/- preadipocytes, mitochondrial transfer failed to rescue adipogenesis, indicating that mitochondrial mass expansion alone is insufficient to reverse the mechanisms leading to lipodystrophy in this model. These results indicate that, although exogenous human and murine mitochondria can be incorporated into the mitochondrial network of differentiating adipocytes, they do not directly influence the adipogenic program.

引言

Beyond their primary bioenergetic roles, mitochondria serve as signaling hubs in multiple cellular processes, including cell differentiation^1,2,3,4. Brown adipose tissue (BAT) possesses a notably high mitochondrial mass to support its thermogenic activity, highlighting its role in whole-body energy balance and in the pathogenesis of obesity⁵. While mitochondrial mass is regulated by the balance between biogenesis and mitophagy, it remains unclear whether mitochondrial mass expansion during brown adipocyte differentiation is functionally required for adipogenesis or merely a consequence of the process.

Physiological mitochondrial transfer between cells has been documented both in vitro and in vivo, where it contributes to tissue adaptation under pathological conditions, including adipose tissue dysfunction associated with obesity and insulin resistance^6,7. Furthermore, artificial mitochondrial transfer in vitro has been shown to enhance the respiratory capacity of recipient cells⁸. Together, these findings support the concept that mitochondrial transfer can modify cellular metabolic function and may contribute to tissue adaptation under conditions of bioenergetic stress^9,10,11. Compared with pharmacological or genetic strategies that stimulate endogenous mitochondrial biogenesis by activating nuclear and mitochondrial transcriptional programs, mitochondrial transfer directly delivers organelles to recipient cells, enabling rapid modification of mitochondrial mass independently of transcriptional manipulations^12,13. This approach is critical for correcting defects in mitochondrial diseases but also allows to study mitochondrial actions without the potential off-target effects of pharmacological or genetic approaches¹⁴.

In the present study, we investigated the effect of artificially increasing the mitochondrial mass by exogenous mitochondrial transfer in differentiating brown adipocytes. This approach enabled direct assessment of the impact of mitochondrial mass on the adipogenic program. To achieve this, mitochondrial transfer protocols originally developed for mesenchymal stem cells were adapted¹⁵ using both human hepatic cells and murine preadipocytes as mitochondrial donors. A method for tracking human mitochondria in differentiating mouse cells was developed using genetic tools combined with imaging techniques, demonstrating that mitochondria from both origins are incorporated into the endogenous mitochondrial network and persist throughout adipogenic differentiation.

To model defective adipogenesis associated with low mitochondrial mass, differentiating brown adipocytes derived from 1-acylglycerol-3-phosphate-O-acyltransferase 2 (AGPAT2)-deficient (Agpat2^-/-) mice were used. AGPAT2 is highly expressed in adipose tissue, where it catalyzes the formation of phosphatidic acid in the glycerolipid biosynthesis pathway. AGPAT2 deficiency causes severe lipodystrophy in both humans and mice and impairs adipogenesis in white and brown adipocyte models in association with reduced mitochondrial mass^16,17,18. Incorporation of exogenous mitochondria into differentiating preadipocytes slightly altered lipid droplet size distribution but did not increase the expression of mature brown adipocyte markers or rescue the adipogenic impairment of Agpat2^-/- preadipocytes.

方案

Animal procedures were approved by the Institutional Animal Care and Use Committee at Pontificia Universidad Católica de Chile, protocol 210609003. Wild-type and Agpat2^-/- P0.5 neonatal mice of both sexes, derived from a mixed C57BL/6J and 129J genetic background, were used in this study. Personal Protective Equipment (PPE): Wear a laboratory coat, safety glasses, and nitrile gloves. See Supplemental File 1 for additional protocol details and Table 1 for the buffers required for this protocol.

All toxic chemical waste generated during electron microscopy preparation, paraformaldehyde fixation, and nucleic acid extraction must be strictly segregated into designated, clearly labeled streams in compliance with institutional Environmental Health and Safety (EHS) regulations. Under no circumstances should any of these reagents be discharged into the laboratory sink or public sewage system. All hazardous chemical waste generated must be segregated according to institutional EHS classifications.

1. Cell culture

1. Isolation, differentiation, and maintenance of primary adipocytes (iBAT)
   NOTE: See Supplemental File 1 for a brief description of the procedures and Table 1 for the composition of the required solutions. A complete and detailed explanation of our in vitro brown adipogenic differentiation protocol can be found in Figueroa et al.¹⁹.
   1. Isolate preadipocytes from the interscapular brown adipose tissue (iBAT) of neonatal (P0.5) mice following the surgical and enzymatic digestion procedures described by Figueroa et al.¹⁹.
   2. Differentiate and maintain the brown adipocyte culture according to the differentiation cocktail and media exchange schedule.
      NOTE: For a successful adipogenic differentiation, it is critically important that cultures reach 90–100% confluence before initiating the adipogenic induction.
2. HepG2 culture
   1. Culture HepG2 cells in DMEM supplemented with 10% fetal bovine serum, 100 U/mL penicillin, 100 µg/mL streptomycin, and 0.25 µg/mL amphotericin B. Maintain the cells at 37 °C in a humidified incubator with 5% CO₂.
      NOTE: These cells grow in clusters and may appear subconfluent despite high density due to multilayered growth.

2. Mitochondrial isolation and transference

1. Mitochondrial isolation
   NOTE: Perform all steps in a biosafety cabinet at 4 °C or on ice. Use the preparation within 2 h.
   1. Seed 2 × 10⁶ donor cells (HepG2 or preadipocytes) in 100 mm culture dishes. Grow cells until they reach 80% (HepG2) or 100% (preadipocytes) confluence.
   2. Stain donor cells with 100 nM MitoTracker Deep Red FM in FBS-free medium for 30 min at 37 °C in a 5% CO₂ incubator.
   3. Wash the cells 2x with growth medium to remove excess dye.
   4. Detach cells using trypsin, collect the suspension, and centrifuge at 300 × g for 5 min at 4 °C.
   5. Resuspend the pellet in 1 mL of mitochondrial isolation buffer (MIB) supplemented with BSA, protease inhibitors, and phosphatase inhibitors. Disrupt the plasma membrane by passing the suspension through a tuberculin syringe 5x. Homogenize the suspension by passing it through an insulin syringe at least 10x until the solution is light-brown and lacks visible clumps.
      NOTE: For western blot analysis, aliquot 50 µL of the total lysate and store at -20 °C.
2. Centrifuge the homogenate at 900 × g for 11 min at 4 °C.
   NOTE: If the supernatant after the 900 × g spin is not cloudy, cellular lysis is likely incomplete.
   1. Collect the supernatant and centrifuge at 10,000 × g for 10 min at 4 °C to pellet the mitochondria. Wash the mitochondrial pellet 3x with MIB supplemented with BSA.
   2. Perform a final resuspension in 100 µL of BSA-free MIB. Quantify protein concentration using a BCA protein assay.
3. Mitochondrial transfer assay (MTA) in preadipocytes
   1. Seed recipient preadipocytes at 5 × 10⁵ cells/well in 12-well plates (with 18 mm coverslips for microscopy) 24 h prior to the assay.
   2. Add isolated donor mitochondria directly to the recipient medium at a ratio of 10 µg of mitochondrial protein per 10⁵ cells. Rock the plates gently to distribute the mitochondria. Incubate cells for 24–120 h (corresponding to days 1, 3, and 5 of differentiation) at 37 °C in a humidified incubator with 5% CO₂ prior to analysis.

3. Mitochondrial oxygen consumption and MTA efficiency

1. Mitochondrial respirometry
   1. Set the external circulating water bath to 25 °C and ensure stable thermal equilibrium in the chamber jacket before initiating any measurements.
   2. Perform a two-point liquid phase calibration using the instrument's acquisition software.
      1. Air-saturation calibration (High Point): Add 500 µL of air-saturated demineralized water to the chamber. Set the magnetic stirrer to 60 rpm and record the signal until it stabilizes at a plateau (>1,500 mV).
      2. Zero-oxygen calibration (Low Point): Add a small (~3 mm diameter) amount of sodium sulfite to the chamber to displace any remaining air. Record until the signal drops to a stable baseline plateau (~1% of the basal signal, ~20 mV).
   3. Initiate real-time recording (total run time: ~10 min).
   4. Record for 3 min until a stable linear reading is achieved.
   5. Resuspend isolated mitochondria in 200 µL of mitochondrial assay buffer (MAS)²⁰ supplemented with 5 mM glutamate and 2.5 mM malate.
      NOTE: For the present work, the pellet of total mitochondria was extracted from two 100 mm cell-plates.
   6. Transfer the suspension to the Oxygraph chamber and close the chamber sealing plunger tightly, ensuring no air bubbles remain.
   7. Record oxygen consumption for 3 min.
   8. Add 150 µM ADP to trigger mitochondrial coupled respiration and measure ATP synthesis-coupled respiration for 3 min.
   9. Manually define the stable, linear segments corresponding to each respiratory phase. Extract the automated slope values calculated by the software, expressed as oxygen consumption rates in nmol∙mL^-1∙min^-1.
      NOTE: For interplate chamber cleaning, rinse the chamber 2x with 1 mL of demineralized water and ensure the interior is completely dry. Add 100 µL of PBS to the chamber before proceeding to the next plate.
2. Flow cytometry
   NOTE: Keep all samples on ice throughout the procedure to preserve cellular and bioenergetic integrity.
   1. Isolate mitochondria and perform mitochondrial transfer assay (MTA), as described in Sections 2.1 and 2.2, respectively, in 35 mm culture dishes, using donor cells previously labeled with MitoTracker Deep Red FM.
   2. Aspirate the culture medium and wash the cell monolayer once with 1 mL of sterile PBS.
   3. Add 500 µL of 0.25% Trypsin-EDTA and incubate the dishes at 37 °C until complete cell detachment is observed under a microscope.
   4. Neutralize trypsin by adding 1 mL of complete growth medium (DMEM with 10% FBS). Transfer the entire volume to a 15 mL conical tube and centrifuge at 300 × g for 5 min at 4 °C.
   5. Discard the supernatant by aspiration and retain the cell pellet. Resuspend the pellet in 500 µL of ice-cold PBS by gentle pipetting.
   6. Analyze the samples using a flow cytometer equipped with a 640 nm laser (see Supplemental File 1 for details on flow cytometry acquisition and analysis).
      1. Define the cell population using Forward Scatter (FSC) vs. Side Scatter (SSC) plots and apply a gating strategy to exclude debris and cell doublets.
      2. Quantify the fluorescence intensity in the far-red channel (670/30 nm emission filter) to detect internalized MitoTracker-labeled mitochondria.
      3. Perform analysis using Floreada.io (see Supplemental File 1 for gating protocol details).
         NOTE: Include a negative control (recipient cells without MTA) to set the baseline for background auto-fluorescence.
3. Confocal and electron microscopy
   1. Live cell imaging assay
      1. Seed primary preadipocytes derived from P0.5 neonatal mice into 12-well plates containing 18 mm coverslips, following the specific cell density and media requirements detailed in Section 1.
      2. Isolate mitochondria and execute the mitochondrial transfer assay (MTA) using donor cells previously labeled with MitoTracker Deep Red FM, as specified in Section 2.
      3. Maintain the recipient cultures in a humidified incubator at 37 °C with 5% CO₂ for 24 h to allow for mitochondrial uptake.
      4. Prepare a 70 nM MitoTracker Green working solution by diluting the stock in FBS-free culture medium.
      5. Aspirate the growth medium from the 12-well plates and replace it with the 70 nM MitoTracker Green solution. Incubate the plates for 25 min at 37 °C in a humidified incubator with 5% CO₂ to counterstain the total mitochondrial network.
      6. Remove the staining solution and wash the coverslips 2x with 1 mL of warm, complete culture medium.
      7. Replace the final volume with phenol red-free complete medium to minimize background auto-fluorescence during acquisition.
      8. Transfer the coverslips or the plate to the confocal microscope stage. Set the microscope’s incubation chamber to maintain a constant environment of 37 °C and 5% CO₂.
      9. Capture images immediately using appropriate excitation/emission settings for both far-red (MitoTracker Deep Red FM) and green (MitoTracker Green) channels. See Supplemental File 1 for additional details.
         NOTE: Perform all staining and handling steps under low-light conditions to prevent photobleaching of the fluorophores. Use a high-numerical aperture (NA) oil-immersion objective (60x or 100x) for optimal resolution of mitochondrial morphology.
   2. Confocal immunofluorescence assay with fixed cells
      NOTE: Following cell fixation, toxic paraformaldehyde and glutaraldehyde solutions are classified as non-halogenated organics. Nucleic acid extraction byproducts require strict segregation: phenol/chloroform mixtures must be disposed of as halogenated organics, while guanidinium-based buffers are classified as corrosive organics.
      1. Seed primary preadipocytes derived from P0.5 neonatal mice into 12-well plates containing 12 mm coverslips, as described in Section 1.
      2. Isolate mitochondria and perform the mitochondrial transfer assay (MTA) following the procedures specified in Section 2.
      3. Incubate the cultures for 24 h to allow for mitochondrial uptake.
      4. Induce brown adipogenic differentiation by following the protocol described in Supplemental File 1 and refer to Table 1 for the required buffers’ composition.
      5. Fix the cells on day 7 of differentiation (168 h). Aspirate the culture medium and add 500 µL of 4% paraformaldehyde (PFA) per well. Incubate for 20 min at room temperature.
      6. Wash the coverslips 2x by adding 1 mL of ice-cold PBS per well. Permeabilize and block the cells by incubating the coverslips in PBS containing 0.05% saponin and 0.2% BSA for 1 h at room temperature. Place the plate on an orbital shaker under gentle agitation.
      7. Wash the cells 2x with 1 mL of PBS. Stain the nuclei and lipid droplets simultaneously. Apply 1 µg/mL Hoechst 33342 and 1 µg/mL BODIPY prepared in the blocking/permeabilization buffer. Incubate for 30 min at room temperature, ensuring the plate is protected from light.
      8. Wash the coverslips 2x with 1 mL of ice-cold PBS. Mount the coverslips onto clean glass slides. Dispense 10 µL of mountant onto the slide and place the coverslip cell-side down onto the mounting medium. Allow the samples to dry overnight in a dark environment at room temperature before imaging.
      9. Acquire images using a confocal microscope. Use two fluorescence channels calibrated for the emission spectra of Hoechst and BODIPY. See Supplemental File 1 for additional imaging details.
      10. Perform lipid droplet analysis using ImageJ v1.54s. Open the lipid droplet channel, identify individual droplets manually using the Freehand selections and ROI Manager tools, and calculate the droplet area using the Analyze | Measure command.
      11. Process and analyze the resulting data using the R scripts provided in Supplemental File 2 within the RStudio v4.5.2 environment.
          NOTE: Acquire exactly five images per coverslip at 10x magnification to ensure representative sampling. Use R version 4.5.2 or higher for compatibility with the provided scripts.
   3. Transmission electron microscopy (TEM)
      NOTE: For electron microscopy byproducts, highly toxic osmium tetroxide and arsenic-containing sodium cacodylate buffers must be collected as toxic heavy metal waste, whereas uranyl acetate is managed separately as radioactive heavy metal waste under institutional radiation safety protocols.
      1. Centrifuge the isolated mitochondria, from Section 2, at 10,000 × g for 10 min at 4 °C to obtain a compact pellet.
      2. Fix the pellet by adding 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer (pH 7.0). Incubate for 2 h at 4 °C.
         NOTE: Always handle glutaraldehyde stock solutions and perform initial fixation steps inside a chemical fume hood. Wear nitrile gloves and goggles for eye protection. Avoid any contact with heating sources, as heated glutaraldehyde releases highly irritating vapors.
      3. Wash the mitochondrial preparation for 3 × 10 min with 0.05 M sodium cacodylate buffer, and centrifuge briefly to retain the pellet between buffer changes.
      4. Post-fix the sample by adding 1% aqueous osmium tetroxide (OsO₄). Incubate for 15 min at room temperature.
         NOTE: Osmium tetroxide must only be opened and handled inside a certified, fully functional chemical fume hood. Wear a lab coat, safety goggles or a full-face shield, and thick or double-nitrile gloves (change gloves immediately if any splash occurs, as OsO₄ can penetrate thin nitrile over time).
      5. Wash the sample for 3 × 5 min with double-distilled water. Stain the pellet with 1% aqueous uranyl acetate for 15 min.
         NOTE: Work on disposable plastic-backed bench paper. Dedicate a specific area of the lab for radioactive staining. Wear double gloves, a lab coat, and safety goggles. Wash hands thoroughly after completing the procedure.
      6. Dehydrate the preparation using a graded ethanol series. Incubate the pellet in 30%, 50%, 70%, 95%, and 100% ethanol for 5 min at each concentration.
      7. Embed the mitochondrial fractions. Incubate in a 1:1 Epon/ethanol solution for 30 min, followed by pure Epon resin for 1 h.
      8. Transfer the samples to embedding molds and polymerize in a 60 °C oven for 48 h.
      9. Attach the resin blocks to the ultramicrotome and cut ultrathin sections (80 nm).
      10. Collect sections onto grids. Stain the grids with 1% aqueous uranyl acetate for 4 min. Rinse with double-distilled water.
      11. Stain with lead citrate for 5 min following Reynolds’ method²¹. Rinse thoroughly. Visualize the grids using the TEM. See Supplemental File 1 for details on the Reynolds’ method and TEM image acquisition.

4. Molecular quantification

1. Mitochondrial DNA (mtDNA) standard curve
   1. Seed HepG2 cells into five 100 mm culture dishes. Incubate the cultures until they reach 80% of confluence.
   2. Isolate the mitochondria from the harvested cells by following the technical procedure detailed in Section 2.
   3. Extract total DNA from the resulting mitochondrial pellet using the acid-guanidinium-phenol-chloroform method as described in Section 4.2.6. Measure the DNA concentration and evaluate purity ((A₂₆₀/A₂₈₀ and (A₂₆₀/A₂₃₀ ratios) using a microvolume UV-Vis spectrophotometer.
   4. Prepare a serial dilution series using nuclease-free water as the diluent. Dilute the DNA stock to achieve final amounts of 1, 10^-1, 10^-2, 10^-3, 10^-4, and 10^-5 ng per reaction volume. Vortex each dilution for 5 s to ensure complete homogeneity before proceeding to the next step in the series.
      NOTE: Adjust the concentration range of the standard curve based on the specific sample concentration and the final PCR reaction volume.
2. Detection of Human mtDNA in recipient cells
   1. Seed primary preadipocytes derived from P0.5 neonatal mice into 60 mm culture dishes, following the density and media conditions specified in Section 1.
   2. Isolate mitochondria from donor HepG2 cells and execute the mitochondrial transfer assay (MTA) as detailed in Section 2.
   3. Incubate the cultures for 24 h at 37 °C and 5% CO₂.
   4. Induce brown adipogenic differentiation for 24–120 h (at days 1, 3, and 5) by following the media exchange protocol described in Section 1.
   5. Aspirate the culture medium and wash the cells 2x with 2 mL of ice-cold PBS.
   6. Extract total DNA using the acid-guanidinium-phenol-chloroform method²².
      NOTE: Always aliquot and perform phase separation inside the fume hood to avoid inhaling toxic phenol vapors. Use double-nitrile gloves or heavy-duty chemical-resistant gloves.
   7. Perform phase separation and discard the entire aqueous phase located above the interphase.
      CRITICAL STEP: Remove the aqueous phase completely to prevent contamination and ensure high DNA purity for downstream qPCR.
   8. Add 0.3 mL of 100% ethanol per 1 mL of the initial extraction reagent. Cap the tube and mix vigorously by inversion.
   9. Let it stand for 3 min at room temperature and centrifuge at 2,000 × g for 5 min at 4 °C to pellet the DNA.
   10. Transfer the phenol–ethanol supernatant to a separate tube for potential protein isolation. Resuspend the DNA pellet in 1 mL of 0.1 M sodium citrate (in 10% ethanol, pH 8.5) per 1 mL of extraction reagent used.
   11. Let it stand for 30 min at room temperature, gently inverting it a few times, and centrifuge at 2,000 × g for 5 min at 4 °C. Discard the supernatant.
   12. Repeat the sodium citrate wash steps two additional times.
   13. Wash the resulting pellet with 2 mL of 75% ethanol per 1 mL of initial extraction reagent.
   14. Let it stand for 20 min at room temperature and centrifuge at 2,000 × g for 5 min at 4 °C.
   15. Discard the supernatant and air-dry the pellet for 10 min. Solubilize the DNA by adding 0.3–0.6 mL of 8 mM NaOH and pipetting up and down repeatedly until the pellet disappears.
   16. Centrifuge at 12,000 × g for 10 min at 4 °C to remove any insoluble debris. Transfer the supernatant to a sterile tube and adjust the pH to 7–8 using HEPES.
   17. Measure DNA concentration and purity ((A(260)/A(280) and (A(260)/A(230) ratios) using a microvolume UV-Vis spectrophotometer.
   18. Dilute the template to a final amount of 15 ng of total DNA in nuclease-free water. Perform quantitative real-time PCR (qPCR) for human mtDNA using optical 96-well plates as specified in Section 4.3.
   19. Analyze the amplification results by applying a logarithmic regression model.
       NOTE: Conduct the logarithmic regression analysis using DNA concentration and corresponding threshold cycle (Ct) values as variables.
3. RT-qPCR for gene expression
   1. Cell preparation and differentiation
      1. Seed primary preadipocytes derived from P0.5 neonatal mice in 60 mm culture dishes as detailed in Section 1.1.
      2. Isolate mitochondria and perform the mitochondrial transfer assay (MTA) following the procedures in Section 2. Incubate the cultures for 24 h.
      3. Induce brown adipogenesis for 24–120 h (sampling at days 1, 3, and 5 of differentiation) according to the protocol in Section 1.
   2. Total RNA isolation
      1. Remove the culture medium and add 1 mL of Acid-guanidinium-phenol-chloroform extractant reagent per 1 × 10⁶ cells directly to the dish. Homogenize the samples by repeated pipetting until the lysate is uniform.
         NOTE: Always aliquot and perform phase separation inside the fume hood to avoid inhaling toxic phenol vapors. Use double-nitrile gloves or heavy-duty chemical-resistant gloves.
      2. Add 0.2 mL of chloroform per 1 mL of extractant reagent used. Cap the tubes securely and shake vigorously by hand for 15 s. Let it stand for 3 min at room temperature and centrifuge at 12,000 × g for 15 min at 4 °C.
      3. Transfer the upper aqueous phase carefully to a new nuclease-free tube. Avoid contact with the interphase. Keep the samples on ice.
      4. Add 0.5 mL of isopropanol per 1 mL of extractant reagent used. Mix gently by inversion and incubate for 10 min at room temperature.
      5. Centrifuge at 12,000 × g for 10 min at 4 °C to pellet the RNA. Discard the supernatant by inversion.
      6. Wash the RNA pellet with 1 mL of 75% ethanol. Vortex briefly and centrifuge at 7,500 × g for 5 min at 4 °C.
      7. Discard the supernatant and air-dry the RNA pellet for 10 min at room temperature. Resuspend the pellet in 30 µL of nuclease-free water. Incubate the samples at 60 °C for 15 min to ensure complete solubilization.
      8. Determine RNA concentration and purity (A₂₆₀/A₂₈₀ ratios) using a microvolume UV-Vis spectrophotometer.
      9. Verify RNA integrity via agarose gel electrophoresis.
   3. DNase treatment
      1. Add 0.1 volumes of 10× DNase buffer and 1 µL of DNase enzyme to each RNA sample. Mix gently by pipetting. Incubate the reactions at 37 °C for 30 min.
      2. Resuspend the DNase Inactivation Reagent by flicking or vortexing until the slurry is homogeneous. Add the Inactivation Reagent (0.1 volumes of the RNA sample or 2 µL, whichever is greater) and mix thoroughly. Incubate for 5 min at room temperature. Flick the tubes 3x during this period to maintain the reagent in suspension.
      3. Centrifuge at 10,000 × g for 1.5 min. Transfer the RNA-containing supernatant to a new tube.
         CRITICAL STEP: Ensure no DNase Inactivation Reagent is carried over, as it inhibits subsequent cDNA synthesis.
   4. Reverse transcription (RT)
      1. Quantify the treated RNA and dilute in nuclease-free water to use up to 2 µg of total RNA per 20 µL reaction.
      2. Prepare the RT master mix on ice following the manufacturer’s instructions. Dispense the mix into reaction tubes and add the RNA samples.
      3. Load into a thermal cycler and run the reverse transcription program as specified by the kit manufacturer.
   5. Quantitative real-time PCR (qRT-PCR)
      1. Use the cDNA generated in Section 4.3.4 as the PCR template. Dilute the cDNA in nuclease-free water to a working concentration of 20 ng per 10 µL reaction. Keep all the reagents on ice.
      2. Prepare a master mix containing SYBR Green, primers, and nuclease-free water. Include excess volume for pipetting loss. Dispense 10 µL of the reaction mixture into each well of an optical qPCR plate.
      3. Seal the plate with optical adhesive film and centrifuge briefly to collect the liquid at the bottom. Load the plate into a real-time PCR instrument and perform amplification using fast cycling mode.
      4. Determine the threshold cycle (Ct) values and perform relative quantification using the ΔΔCt method. Include a melting curve analysis at the end of the run to verify amplification specificity.
         NOTE: Normalize target mRNA abundance to 36B4 mRNA levels as the endogenous housekeeping gene. Run the qPCR plates within 2 h of setup; otherwise, store the sealed plates at 4 °C.
4. Western blot
   1. Quantify protein concentration from whole-cell and mitochondrial extracts (refer to Sections 2.1.8 and 2.1.12) using a BCA assay.
   2. Prepare 30 µg of protein per sample and add the appropriate volume of SDS-PAGE sample loading buffer (e.g., Laemmli buffer).
   3. Denature the samples by heating at 95 °C for 5 min (or follow specific temperature requirements for membrane proteins.
   4. Load the samples into the wells of a polyacrylamide gel. Separate proteins by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE) at a constant voltage (e.g., 80–120 V) until the dye front reaches the bottom of the gel.
   5. Activate a PVDF membrane by immersing it in 100% methanol for 1 min, followed by equilibration in transfer buffer.
   6. Assemble the transfer sandwich, ensuring the absence of air bubbles between the gel and the membrane.
   7. Transfer the proteins onto the PVDF membrane by electroblotting at 400 mA for 2 h. Maintain the system at 4 °C throughout the process.
   8. Block non-specific binding sites by incubating the membrane in 5% non-fat milk prepared in Tris-buffered saline containing 0.1% Tween 20 (TBS-T) for 1 h at room temperature.
   9. Incubate the membrane with primary antibodies (diluted 1:1,000 in blocking solution) overnight at 4 °C under gentle agitation.
   10. Wash the membrane 3 × 15 min with TBS-T.
   11. Incubate with horseradish peroxidase (HRP)-conjugated secondary antibodies for 2 h at room temperature.
   12. Wash the membrane 3x with TBS-T, followed by a final 5-min wash with 1× TBS.
   13. Visualize the protein bands using an enhanced chemiluminescence (ECL) substrate. Capture the signal using a digital imaging system.
       NOTE: Adjust the polyacrylamide gel percentage (e.g., 8%, 10%, or 12%) based on the molecular weight of the target proteins. If the electrotransfer apparatus lacks an active cooling system, replace ice containers every hour and keep the chamber submerged in an ice bath. Store membranes in 1× TBS at 4 °C if visualization is delayed.

结果

Mitochondrial extraction and structural and respiratory integrity

To evaluate the impact of increased mitochondrial mass on brown adipogenesis, a mitochondrial transfer assay (MTA) was performed in undifferentiated preadipocytes (Figure 1A). Mitochondria were isolated from primary murine preadipocytes (mMito) and from the human hepatic HepG2 cell line (hMito). Western blot analysis demonstrated that both preparations were highly enriched in the mi...

讨论

Biological implications of mitochondrial transfer in adipogenesis

Our results show that although exogenous mitochondria from both human and murine sources can be incorporated into the endogenous mitochondrial network of differentiating preadipocytes, an artificial increase in mitochondrial mass is insufficient to drive the brown adipogenic program. These findings suggest that the mitochondrial expansion characteristic of brown adipogenesis is a consequence of cellular differe...

材料

本文使用的材料清单

姓名	公司	目录编号	评论
100 mm板	SPL生命科学	10101SPL
10x Tris/甘氨酸缓冲液	BioRad	1610734
12 mm玻璃盖玻片	Marienfeld	111520
12孔板	SPL生命科学	30012SPL
16% 甲醛水溶液	Invitrogen	28908
18 mm玻璃盖玻片	HART	-
24孔板	SPL生命科学	30024SPL
3,3',5-三碘-L-甲状腺素钠盐 (T3)	Sigma	T6397
3-异丁基-1-甲基黄嘌呤（IBMX）	Calbiochem	410957
30% 丙烯酰胺/双丙烯酰胺溶液，37.5:1	BioRad	1610158
35 mm板	SPL生命科学	20035SPL
6孔板	SPL生命科学	30006SPL
60 mm培养皿	SPL生命科学	20060SPL	用于初级前脂肪细胞和 DNA/qPCR 实验; 供应商/编号未提供
AccuRuler RGB Plus 预染蛋白标准	Maestrogen	02102-250
ACK 裂解缓冲液	Gibco	A10492-01
Actrapid 100 UI/mL (胰岛素)	Novo Nordisk	A10AB01
ADP	Merck	117105
琼脂糖	FERMELO BIOTEC	FER00AL200G	用于 RNA 完整性验证; 供应商/编号未提供
铵过硫酸盐	BioRad	1610700
抗兔 IgG, HRP 连接抗体	Cell Signaling	7074
抗大鼠 IgG, HRP 连接抗体	Cell Signaling	7077
抗生素-抗真菌剂	Gibco	15240062
Axio Observer 倒置显微镜支架	Carl Zeiss	431007-9901-000	从补充方法中添加
BCA 蛋白测定试剂盒	Thermo Scientific	D49328
BD 细胞仪设置和追踪珠	BD Biosciences	-	从补充方法中添加; 编号未提供
BD FACSDiva 软件 v8.0.3	BD Biosciences	-	从补充方法中添加
BD LSRFortessa X-20 细胞分析仪	BD Biosciences	-	现有条目标准化以匹配补充文件
BioRender	BioRender	-	用于创建图 1 工作流程
Blotting 级阻滞剂	BioRad	170-6404
BODIPY 493/503	Invitrogen	D3922
牛血清白蛋白 (BSA)	Sigma	A1470
CaCl2	Calbiochem	208291
cDNA 逆转录试剂盒	Invitrogen	4374966
细胞筛 100 μm, 尼龙	Falcon	352360
细胞筛 40 μm, 尼龙	Falcon	352340
II 型胶原酶	Gibco	17101-015
地塞米松	Sigma	D4902
DMEM 粉末, 高葡萄糖, 丙酮酸	Thermo Scientific	12800017
DMEM/F-12, 不含苯酚红	Thermo Scientific	21041025
DMEM/F-12, 粉末	Gibco	12500062
DMSO	Sigma	D8418	诱导培养基的溶剂; 供应商/编号未提供
EMBed-812 包埋套装 (Epon)	Electron Microscopy Sciences	14120
绝对乙醇	Merck	100983
乙二醇-双(β-氨乙基醚)-N,N,N',N'-四乙酸四钠盐 (EGTA)	Merck	324626
FAST SYBR MASTER MIX	Thermo Scientific	4385612
FCCP	Sigma	C2920
胎牛血清	Capricorn Scientific	BS-16A
Floreada.io	Floreada.io	-	流式细胞术分析软件
Fluoromount-G	Thermo Scientific	7984-25
GAPDH 抗体	Santa Cruz	sc-32233
葡萄糖	Gibco	15023-021
谷氨酸	Sigma	G1626
25% 丙烯醛水溶液	Electron Microscopy Sciences	16210
山羊抗小鼠 IgG (H+L) 次级抗体, HRP	Invitrogen	62-6520
GraphPad Prism v10.6.1	GraphPad Software	-	统计/对数回归分析软件
Halt 蛋白酶和磷酸酶抑制剂鸡尾酒 100X	Thermo Scientific	78442
HEPES	Biological Industries	41-122-100
组蛋白 H3 (1G1)	Santa Cruz	sc-517576
Hoechst 33342	Life Technologies	H3570
ImageJ v1.54s	NIH	-	脂滴图像分