TY - JOUR
T1 - Ultrasound-assisted liposuction provides a source for functional adipose-derived stromal cells
AU - Duscher, Dominik
AU - Maan, Zeshaan N.
AU - Luan, Anna
AU - Aitzetmüller, Matthias M.
AU - Brett, Elizabeth A.
AU - Atashroo, David
AU - Whittam, Alexander J.
AU - Hu, Michael S.
AU - Walmsley, Graham G.
AU - Houschyar, Khosrow S.
AU - Schilling, Arndt F.
AU - Machens, Hans Guenther
AU - Gurtner, Geoffrey C.
AU - Longaker, Michael T.
AU - Wan, Derrick C.
N1 - Publisher Copyright:
© 2017 International Society for Cellular Therapy
PY - 2017/12
Y1 - 2017/12
N2 - Background aims Regenerative medicine employs human mesenchymal stromal cells (MSCs) for their multi-lineage plasticity and their pro-regenerative cytokine secretome. Adipose-derived mesenchymal stromal cells (ASCs) are concentrated in fat tissue, and the ease of harvest via liposuction makes them a particularly interesting cell source. However, there are various liposuction methods, and few have been assessed regarding their impact on ASC functionality. Here we study the impact of the two most popular ultrasound-assisted liposuction (UAL) devices currently in clinical use, VASER (Solta Medical) and Lysonix 3000 (Mentor) on ASCs. Methods After lipoaspirate harvest and processing, we sorted for ASCs using fluorescent-assisted cell sorting based on an established surface marker profile (CD34+CD31–CD45–). ASC yield, viability, osteogenic and adipogenic differentiation capacity and in vivo regenerative performance were assessed. Results Both UAL samples demonstrated equivalent ASC yield and viability. VASER UAL ASCs showed higher osteogenic and adipogenic marker expression, but a comparable differentiation capacity was observed. Soft tissue healing and neovascularization were significantly enhanced via both UAL-derived ASCs in vivo, and there was no significant difference between the cell therapy groups. Conclusions Taken together, our data suggest that UAL allows safe and efficient harvesting of the mesenchymal stromal cellular fraction of adipose tissue and that cells harvested via this approach are suitable for cell therapy and tissue engineering applications.
AB - Background aims Regenerative medicine employs human mesenchymal stromal cells (MSCs) for their multi-lineage plasticity and their pro-regenerative cytokine secretome. Adipose-derived mesenchymal stromal cells (ASCs) are concentrated in fat tissue, and the ease of harvest via liposuction makes them a particularly interesting cell source. However, there are various liposuction methods, and few have been assessed regarding their impact on ASC functionality. Here we study the impact of the two most popular ultrasound-assisted liposuction (UAL) devices currently in clinical use, VASER (Solta Medical) and Lysonix 3000 (Mentor) on ASCs. Methods After lipoaspirate harvest and processing, we sorted for ASCs using fluorescent-assisted cell sorting based on an established surface marker profile (CD34+CD31–CD45–). ASC yield, viability, osteogenic and adipogenic differentiation capacity and in vivo regenerative performance were assessed. Results Both UAL samples demonstrated equivalent ASC yield and viability. VASER UAL ASCs showed higher osteogenic and adipogenic marker expression, but a comparable differentiation capacity was observed. Soft tissue healing and neovascularization were significantly enhanced via both UAL-derived ASCs in vivo, and there was no significant difference between the cell therapy groups. Conclusions Taken together, our data suggest that UAL allows safe and efficient harvesting of the mesenchymal stromal cellular fraction of adipose tissue and that cells harvested via this approach are suitable for cell therapy and tissue engineering applications.
KW - ASCs
KW - Lysonix
KW - VASER
KW - adipose-derived stromal cells
KW - adult mesenchymal stromal cells
KW - cell therapy
KW - regenerative medicine
KW - ultrasound-assisted liposuction
UR - http://www.scopus.com/inward/record.url?scp=85029225420&partnerID=8YFLogxK
U2 - 10.1016/j.jcyt.2017.07.013
DO - 10.1016/j.jcyt.2017.07.013
M3 - Article
C2 - 28917626
AN - SCOPUS:85029225420
SN - 1465-3249
VL - 19
SP - 1491
EP - 1500
JO - Cytotherapy
JF - Cytotherapy
IS - 12
ER -