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Table 1 The application potential of stem/progenitor cell-derived extracellular vesicles in kidney diseases

From: Application potential of stem/progenitor cell-derived extracellular vesicles in renal diseases

Stem cell type releasing EVs

Animal models

Transferring materials

Target cells

Biogenesis mechanisms

Biological effects

References

EPC

Anti-Thy1.1glomerulonephritis rat model

miRNA

Injured glomerular cells

Inhibit leukocyte infiltration and mesangial cell activation

Improve kidney function

[36]

IRI rat model

miRNA (miR-126 and miR-296)

Hypoxic renal resident cells

Alter the proliferative phenotype of hypoxic renal resident cells and promote angiogenesis

Protect the kidney from ischemic acute injury

[18, 51]

SCID mice

mRNA associated with NOS and PI3K/AKT

ECs

Activate the PI3K/AKT signaling pathway

Trigger neovascularization, promote angiogenesis

[17]

BMMSC

IRI rat model

miR-218

Injured ECs

Enhance endothelial cell migration and stimulate a reparative phenotype

Treat microvascular endothelial injury

[64]

IRI rat model

Chemokine receptors and complement-related proteins

Macrophage and apoptotic cells

Inhibit macrophage activity and promote phagocytosis of apoptotic cells

Prevent early renal injury

[37]

Rat renal transplant model for acute rejection

EVs

–

Induce accumulation of T cells and B cells in renal tissue

Immunomodulatory of the immune system

[41]

IRI rat model

Adhesion molecules, mRNA and miRNA

TECs

Reduce TECs apoptosis and increase TECs proliferation

Protect from AKI and from subsequent chronic renal damage

[62]

Type 2 diabetic mice and insulin-resistant diabetic mice model

EVs

TECs

Suppress the EMT of TECs

Attenuated renal fibrosis

[68]

UUO mouse model

miRNA

Proximal TECs

Enhanced inhibition of TGF-β1-induced EMT

Improve renal function

[66]

UUO mouse model

miRNA-let7c

Damaged kidney cells

Reduce collagen accumulation and fibrotic-related gene expression

Alleviate kidney fibrosis

[80]

hWJMSC

IRI rat model

miRNA

ECs

Inhibit the expression of CX3CL1 and reduce the quantity of CD68+macrophages

Ameliorate renal injury in both the acute and chronic stage

[43]

USC

Type I diabetic rat model

Growth factors, TGF-β1, angiopoietin, and BMP-7

–

Inhibit podocyte apoptosis and promote vascular regeneration and cell survival

Prevent kidney injury from diabetes

[55]

ECFC

IRI rat model

miR-486-5p

ECs

Target at PTEN/Akt pathway

Protect the kidney from IRI injury

[56,57,58]

HLSC

SCID mouse model of AKI

EVs

Tubular cell

Stimulate proliferation and inhibit cell apoptosis

Promote AKI recovery

[59]

GlMSC

IRI rat model

miRNAs

TECs

Activate TEC proliferation

Promote the recovery of AKI

[60]

RCSC

–

HLA-G, costimulatory molecules and adhesion molecules

DCs

Suppress immune response

Tumor immune escape and immune tolerance

[76]

–

Genes associated with matrix remodeling, cell migration, tumor growth, and angiogenesis

MSCs

Induce a pro-tumorigenic phenotype

Promote tumor growth

[77]

RCSC(CD105+ cells)

SCID mice

Proangiogenic mRNA and miRNA

Epithelial cells and ECs

Trigger angiogenesis and promote the formation of premetastatic niche

Promote renal cancer progression and lung metastases

[79]

  1. EVs extracellular vesicles, EPC endothelial progenitor cells, MSC mesenchymal stromal cells, BMMSC bone marrow-derived mesenchymal stem cells, hWJMSC human Wharton-Jelly MSCs, USC urine-derived stem cells, ECFC endothelial colony-forming cells, HLSC human liver stem cells, GlMSC MSC-derived from the glomeruli, RCSC renal cancer stem cells, IRI ischemia-reperfusion injury, SCID severe combined immunodeficient, UUO unilateral ureteral obstruction, AKI acute kidney injury, NOS nitric oxide synthase, BMP-7 bone morphogenetic protein-7, ECs endothelial cells, TECs tubular epithelial cells, DCs dendritic cells, EMT epithelial–mesenchymal transition