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Table 1 Selected cases of modified MSCs application and therapeutic outcome

From: Improved therapeutics of modified mesenchymal stem cells: an update

Modification element

Condition

Results

References

Decorin

Radiation-induced lung injuries

↓Lymphocyte infiltration and apoptosis

↑Proliferation of epithelial cells and inhibition of fibrosis

Effective induction of interferon-γ expression and inhibition of collagen type III α1 expression

[118]

miRNA

Lung fibrosis

Distinctive expression in cytokines and CD45-positive cells

Quick weight gain and improved survival rate

[121]

CCR1

Injured myocardium

Augmented cell survival, migration and engraftment

Significant reduction in infarct size, reduced cardiomyocytes apoptosis and increased capillary density in injured myocardium

Inhibited cardiac remodeling and restored cardiac function 4 weeks after injury

[21]

Betacellulin

Hyperglycemia

Increased insulin production levels

Ameliorated hyperglycemia

[131]

Deferoxamine

Diabetes

Upregulation of CXCR4/CCR2 and higher activity of MMP-2/MMP-9

Increase migration and subsequent homing

[85]

Sox11

Bone fracture

Increased differentiation, migration, and viability of MSCs under oxidative stress

[104]

Activate of BMP/Smad signaling pathway, Runx2, and CXCR4

Accelerating bone fracture healing

ACE2

Injured endothelium

Decreased inflammatory mediators, reduced paracellular permeability, and enhanced survival of endothelial cells

Restore endothelial function

[108]

Integrin α4

Cerebral embolism (stroke)

Increased transendothelial migration of MSCs

Decreased cell aggregation and ameliorated evoked cerebral embolism in stroke rats

[105]

miR‐122

Liver fibrosis

Suppressed the proliferation of and collagen maturation in HSCs

Enhanced the therapeutic efficacy of MSCs

[106]

  1. Different molecules and factors have been associated with modifying MSCs towards encouraging better therapeutic outcome. Applied modified MSCs have been documented across many human conditions in the experimental settings with promising results. This table enlists some of these diseases, elements used in the modification, and the key resultant outputs upon modified MSCs administration
  2. CCR1 c-c chemokine receptor type 1, Sox11 sry-related high-mobility group box 11, BMP bone morphogenetic protein, Runx2 runt-related transcription factor 2, CXCR cxc chemokine receptor, ACE2 angiotensin‐converting enzyme 2, HSCs hepatic stellate cells, MMP matrix metalloproteinase