TY - JOUR
T1 - Donor Sex and Passage Conditions Influence MSC Osteogenic Response in Mineralized Collagen Scaffolds
AU - Kolliopoulos, Vasiliki
AU - Tiffany, Aleczandria
AU - Polanek, Maxwell
AU - Harley, Brendan A. C.
N1 - Research funding
National Institute of Dental and Craniofacial Research. Grant Numbers: R21 DE026582, R01 DE030491
National Institute of Arthritis and Musculoskeletal and Skin Diseases. Grant Number: R01 AR077858
Chemistry-Biology Interface Research Training Program at the University of Illinois. Grant Number: T32 GM070421
Carl R. Woese Institute for Genomic Biology
Chemical and Biomolecular Engineering Dept. at the University of Illinois at Urbana-Champaign
National Science Foundation. Grant Numbers: DGE-1746047, DGE-1144245
National Institutes of Health,. Grant Number: T32 GM070421
PY - 2024/7/22
Y1 - 2024/7/22
N2 - Contemporary tissue engineering efforts often seek to use mesenchymal stem cells (MSCs) due to their multi-potent potential and ability to generate a pro-regenerative secretome. While many have reported the influence of matrix environment on MSC osteogenic response, few have investigated the effects of donor and sex. Here, a well-defined mineralized collagen scaffold is used to study the influence of passage number and donor-reported sex on MSC proliferation and osteogenic potential. A library of bone marrow and adipose tissue-derived stem cells from eight donors to examine donor viability in osteogenic capacity in mineralized collagen scaffolds is obtained. MSCs displayed reduced proliferative capacity as a function of passage duration. Further, MSCs showed significant sex-associated variability in osteogenic capacity. Notably, MSCs from male donors displayed significantly higher cell proliferation while MSCs from female donors displayed significantly higher osteogenic response via increased alkaline phosphate activity, osteoprotegerin release, and mineral formation in vitro. The study highlights the essentiality of including donor-reported sex as an experimental variable and reporting culture expansion in future studies of biomaterial regenerative potential.
AB - Contemporary tissue engineering efforts often seek to use mesenchymal stem cells (MSCs) due to their multi-potent potential and ability to generate a pro-regenerative secretome. While many have reported the influence of matrix environment on MSC osteogenic response, few have investigated the effects of donor and sex. Here, a well-defined mineralized collagen scaffold is used to study the influence of passage number and donor-reported sex on MSC proliferation and osteogenic potential. A library of bone marrow and adipose tissue-derived stem cells from eight donors to examine donor viability in osteogenic capacity in mineralized collagen scaffolds is obtained. MSCs displayed reduced proliferative capacity as a function of passage duration. Further, MSCs showed significant sex-associated variability in osteogenic capacity. Notably, MSCs from male donors displayed significantly higher cell proliferation while MSCs from female donors displayed significantly higher osteogenic response via increased alkaline phosphate activity, osteoprotegerin release, and mineral formation in vitro. The study highlights the essentiality of including donor-reported sex as an experimental variable and reporting culture expansion in future studies of biomaterial regenerative potential.
KW - bone tissue engineering
KW - donor variability
KW - mesenchymal stem cells
KW - sex variation
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U2 - 10.1002/adhm.202400039
DO - 10.1002/adhm.202400039
M3 - Article
C2 - 39036820
SN - 2192-2640
JO - Advanced Healthcare Materials
JF - Advanced Healthcare Materials
M1 - 2400039
ER -