MATR3

Gene

2 papers3 findings

  • 1 lab
  • Animals2

Effects

2

Atherosclerotic lesion area

downin mice1

1 study
  1. MATR3 decreases atherosclerotic lesion area in mice (Deficiency increased lesion area by 1.41-fold).

    “endothelial cell-specific Matrin-3 deficiency increased atherosclerotic lesion area by 1.41-fold”

    Animalsshown by endothelial cell-specific Matrin-3 deficiency in atherosclerosis on a low-density lipoprotein receptor-knockout background

    Protein loss in vessel-lining cells increased plaque area in mice

    FASEB journal : official publication of the Federation of American Societies for Experimental BiologyOct 18, 2026

Cellular senescence

downin human cells1

1 study
  1. MATR3 decreases cellular senescence in human cells.

    “Here, we found that Matrin-3 silencing induces endothelial senescence”

    Cellsshown by Matrin-3 silencingendothelial cell

    Protein loss in vessel-lining cells increased plaque area in mice

    FASEB journal : official publication of the Federation of American Societies for Experimental BiologyOct 18, 2026

More on Cellular senescence

Associations

1

Plasma low-density lipoprotein cholesterol

downin mice1

1 study
  1. MATR3 is associated with plasma low-density lipoprotein cholesterol in mice.

    “was associated with increased plasma low-density lipoprotein cholesterol and triglycerides, increased hepatic cholesterol and triglycerides”

    Animalsshown by endothelial Matrin-3 deficiency in a mouse model of atherosclerosis

    Protein loss in vessel-lining cells increased plaque area in mice

    FASEB journal : official publication of the Federation of American Societies for Experimental BiologyOct 18, 2026

More on Plasma low-density lipoprotein cholesterol

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FASEB Journal

Protein loss in vessel-lining cells increased plaque area in mice

Mice lacking Matrin-3 in vessel-lining cells had a 1.41-fold increase in artery plaque area compared with mice without the deficiency.Mice lacking Matrin-3 in vessel-lining cells had a 1.41-fold increase in artery plaque area compared with mice without the deficiency.

Mouse studyMechanisms