Macrophages are essential for CTGF-mediated adult β-cell proliferation after injury

Molecular Metabolism

Volumn 4, Issue 8, 2015, Pages 584-591

  Riley, Kimberly G ^b   Pasek, Raymond C ^c   Maulis, Matthew F ^c   Dunn, Jennifer C ^c   Bolus, W Reid ^a,b   Kendall, Peggy L ^c   Hasty, Alyssa H ^a,b   Gannon, Maureen ^a,b,c  

^a DEPARTMENT OF VETERANS AFFAIRS   (United States)

^b VANDERBILT UNIVERSITY   (United States)

^c VANDERBILT UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

CTGF; Macrophages; Proliferation; Regeneration; T cells; cell

Indexed keywords

CD19 ANTIGEN; CD38 ANTIGEN; CD40 ANTIGEN; CD45 ANTIGEN; CHEMOKINE RECEPTOR CCR2; COMPLEMENT COMPONENT C3; CONNECTIVE TISSUE GROWTH FACTOR; INTERLEUKIN 12P40; MONOCYTE CHEMOTACTIC PROTEIN 1; PADGEM PROTEIN; RANTES; TUMOR NECROSIS FACTOR ALPHA; VASCULAR CELL ADHESION MOLECULE 1;

ADAPTIVE IMMUNITY; ANTIBODY LABELING; ARTICLE; CD4+ T LYMPHOCYTE; CELL DIVISION; CELL EXPANSION; CELL MATURATION; CELL PROLIFERATION; CELL REGENERATION; CONTROLLED STUDY; DIABETES MELLITUS; EXTRACELLULAR MATRIX; GENE EXPRESSION; GLUCOSE HOMEOSTASIS; HUMAN; HUMAN CELL; IMMUNE SYSTEM; IMMUNOHISTOCHEMISTRY; IMMUNOMODULATION; INNATE IMMUNITY; MACROPHAGE; MACROPHAGE ACTIVATION; PANCREAS ISLET BETA CELL; PHENOTYPE; PRIORITY JOURNAL; T LYMPHOCYTE; T LYMPHOCYTE ACTIVATION; UPREGULATION;

EID: 84937738268     PISSN: None     EISSN: 22128778     Source Type: Journal    
DOI: 10.1016/j.molmet.2015.05.002     Document Type: Article

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