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Table 1 Summary of the mitochondrial transplantation studies described in the present review

From: Therapeutic potential of mitochondrial transplantation in modulating immune responses post-cardiac arrest: a narrative review

Species

Disease models

Targeted organs

Mitochondrial sources

Transplantation methods and timings

Immune response-related outcomes

Refs.

New Zealand white rabbits (male)

Focal ischemia

Heart

Autograft:

Pectoralis major muscle

Direct injection 8 times, 1 min before reperfusion

No significant increase in serum inflammatory markers, No anti-mitochondrial antibodies in serum

[80]

Yorkshire pigs (female)

Focal ischemia

Heart

Autograft:

Pectoralis major muscle

Direct injection 8 times, 1 min before reperfusion

No significant increase in serum cytokines

[81]

Wistar rats (male)

Focal ischemia

Heart

Allograft:

Muscle

Direct injection, upon reperfusion

Modulated autophagic activity, decreased pro-inflammatory cytokines

[71]

1) Wistar rats

2) patient-derived hLCLs

1) Poly I:C MIA

2) Schizophrenia

1) Brain

2) Cell

1) Allograft: Brain

2) hLCLs

1) IC

2) Co-culture

MTx to Poly I:C MIA showed improved immune balance

MTx to healthy hLCLs exhibited immune imbalance, and stress-related chemokine release

[79]

ICR mice (male)

Depression

Brain

Allograft:

Hippocampus

IV, upon or 6 h after LPS injection

Decreased oxidative stress and inflammatory cytokine levels, improved mood-related behavior

[75]

SD rats

Focal ischemia

Spinal cord

Allograft:

Soleus muscle

Direct injection 2 times,

Following SCI

Alleviated cellular apoptosis and inflammation responses

[72]

SD rats (male)

Tendinopathy

Tendon

Allograft:

L6 rat myoblast cell lines

Direct injection, 2 weeks after collagenase injection

Reduced inflammation, and apoptosis; Decreased pro-inflammatory cytokines, increased anti-inflammatory cytokines

[76]

SD rats (male)

Osteoarthritis

Knee joint

BMSCs from tibia and femur

Direct injection into joint cavity,

Once a week for 6 weeks

Increased the production of ATP, inhibited apoptosis, and decreased the production of ROS

[77]

C57BL/6 mice (male)

Sepsis

Whole body

Allograft:

Pectoralis major muscle

IV (tail vein), 120 min after CLP

Reduced inflammation, enhanced bacterial clearance, decreased pro-inflammatory cytokines, and increased anti-inflammatory cytokines

[69]

BALB/C mice (male)

Sepsis

Whole body

UC-MSCs

IV, upon or 30 min after LPS injection

Inhibited the LPS-induced production of pro-inflammatory cytokines/ chemokines, Inhibited the NFκB signaling pathway

[78]

  1. hLCLs human lymphoblastoid cell lines, Poly I:C MIA polyinosinic:polycytidylic acid maternal immune activation, IC intracerebral injection, MTx mitochondrial transplantation, ICV intracerebroventricular injection, IV intravenous injection, LPS lipopolysaccharide, SD Sprague–Dawley, SCI spinal cord injury, BMSCs bone marrow mesenchymal stem cells, ATP adenosine triphosphate, ROS reactive oxygen species, CLP Cecal ligation and puncture, UC-MSCs umbilical cord-derived mesenchymal stem cells, NFκB nuclear factor kappa-light-chain-enhancer of activated B cells