TY - JOUR
T1 - Ligament-derived matrix stimulates a ligamentous phenotype in human adipose-derived stem cells
AU - Little, Dianne
AU - Guilak, Farshid
AU - Ruch, David S.
PY - 2010/7/1
Y1 - 2010/7/1
N2 - Human adipose stem cells (hASCs) can differentiate into a variety of phenotypes. Native extracellular matrix (e.g., demineralized bone matrix or small intestinal submucosa) can influence the growth and differentiation of stem cells. The hypothesis of this study was that a novel ligament-derived matrix (LDM) would enhance expression of a ligamentous phenotype in hASCs compared to collagen gel alone. LDM prepared using phosphate-buffered saline or 0.1% peracetic acid was mixed with collagen gel (COL) and was evaluated for its ability to induce proliferation, differentiation, and extracellular matrix synthesis in hASCs over 28 days in culture at different seeding densities (0, 0.25×106, 1×106, or 2×106 hASC/mL). Biochemical and gene expression data were analyzed using analysis of variance. Fisher's least significant difference test was used to determine differences between treatments following analysis of variance. hASCs in either LDM or COL demonstrated changes in gene expression consistent with ligament development. hASCs cultured with LDM demonstrated more dsDNA content, sulfated-glycosaminoglycan accumulation, and type I and III collagen synthesis, and released more sulfated-glycosaminoglycan and collagen into the medium compared to hASCs in COL (p≤0.05). Increased seeding density increased DNA content incrementally over 28 days in culture for LDM but not COL constructs (p≤0.05). These findings suggest that LDM can stimulate a ligament phenotype by hASCs, and may provide a novel scaffold material for ligament engineering applications.
AB - Human adipose stem cells (hASCs) can differentiate into a variety of phenotypes. Native extracellular matrix (e.g., demineralized bone matrix or small intestinal submucosa) can influence the growth and differentiation of stem cells. The hypothesis of this study was that a novel ligament-derived matrix (LDM) would enhance expression of a ligamentous phenotype in hASCs compared to collagen gel alone. LDM prepared using phosphate-buffered saline or 0.1% peracetic acid was mixed with collagen gel (COL) and was evaluated for its ability to induce proliferation, differentiation, and extracellular matrix synthesis in hASCs over 28 days in culture at different seeding densities (0, 0.25×106, 1×106, or 2×106 hASC/mL). Biochemical and gene expression data were analyzed using analysis of variance. Fisher's least significant difference test was used to determine differences between treatments following analysis of variance. hASCs in either LDM or COL demonstrated changes in gene expression consistent with ligament development. hASCs cultured with LDM demonstrated more dsDNA content, sulfated-glycosaminoglycan accumulation, and type I and III collagen synthesis, and released more sulfated-glycosaminoglycan and collagen into the medium compared to hASCs in COL (p≤0.05). Increased seeding density increased DNA content incrementally over 28 days in culture for LDM but not COL constructs (p≤0.05). These findings suggest that LDM can stimulate a ligament phenotype by hASCs, and may provide a novel scaffold material for ligament engineering applications.
UR - http://www.scopus.com/inward/record.url?scp=77954492887&partnerID=8YFLogxK
U2 - 10.1089/ten.tea.2009.0720
DO - 10.1089/ten.tea.2009.0720
M3 - Article
C2 - 20406104
AN - SCOPUS:77954492887
SN - 1937-3341
VL - 16
SP - 2307
EP - 2319
JO - Tissue Engineering - Part A
JF - Tissue Engineering - Part A
IS - 7
ER -