Human adipose-derived stromal cells accelerate diabetic wound healing: Impact of cell formulation and delivery

Tissue Engineering - Part A

Volumn 16, Issue 5, 2010, Pages 1595-1606

  Amos, Peter J ^a   Kapur, Sahil K ^b   Stapor, Peter C ^a,c   Shang, Hulan ^b   Bekiranov, Stefan ^d   Khurgel, Moshe ^e   Rodeheaver, George T ^b   Peirce, Shayn M ^a   Katz, Adam J ^b  

^a University of Virginia   (United States)

^b UNIVERSITY OF VIRGINIA   (United States)

^c TULANE UNIVERSITY   (United States)

^d UNIVERSITY OF VIRGINIA   (United States)

^e BRIDGEWATER COLLEGE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AGGLOMERATION; ANIMAL CELL CULTURE; BIOACTIVITY; CELLS; ENZYME ACTIVITY; ENZYME INHIBITION; MONOLAYERS; PROTEINS; SUSPENSIONS (FLUIDS);

AFTER-TREATMENT; BIOLOGICAL ACTIVITIES; CELL SUSPENSION; CELL TYPES; CULTURE SUPERNATANT; CUTANEOUS WOUNDS; DELIVERY METHODS; DIABETIC ULCERS; EXTRACELLULAR MATRIX PROTEIN; GENE ARRAYS; HEPATOCYTE GROWTH FACTOR; HUMAN ADIPOSE; IN-VITRO; IN-VIVO; LEPTIN RECEPTORS; MATRIX METALLOPROTEINASE-2; MATRIX METALLOPROTEINASES; MONOLAYER CULTURE; SURGICAL PROCEDURES; TENASCIN; THERAPEUTIC EFFECTS; THERAPEUTIC POTENTIALS; WOUND CLOSURE; WOUND HEALING;

CELL CULTURE;

MUS;

MESSENGER RNA; SCLEROPROTEIN;

ADIPOCYTE; ADIPOSE TISSUE; ANIMAL; ARTICLE; CELL AGGREGATION; CHEMISTRY; CULTURE TECHNIQUE; CYTOLOGY; DIABETES MELLITUS; DRUG DELIVERY SYSTEM; ENZYME LINKED IMMUNOSORBENT ASSAY; GENE EXPRESSION REGULATION; GENETICS; HUMAN; MALE; MASS SPECTROMETRY; METABOLISM; METHODOLOGY; MOUSE; MULTICELLULAR SPHEROID; PATHOLOGY; STROMA CELL; TIME; TRANSPLANTATION; WOUND HEALING;

ADIPOCYTES; ADIPOSE TISSUE; ANIMALS; CELL AGGREGATION; CELL CULTURE TECHNIQUES; DIABETES MELLITUS; DRUG DELIVERY SYSTEMS; ENZYME-LINKED IMMUNOSORBENT ASSAY; EXTRACELLULAR MATRIX PROTEINS; GENE EXPRESSION REGULATION; HUMANS; MALE; MASS SPECTROMETRY; MICE; RNA, MESSENGER; SPHEROIDS, CELLULAR; STROMAL CELLS; TIME FACTORS; WOUND HEALING;

EID: 77953831397     PISSN: 19373341     EISSN: 1937335X     Source Type: Journal    
DOI: 10.1089/ten.tea.2009.0616     Document Type: Article

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