Possibility of using the infrapatellar (Hoffa’s) fat pad as a source of autologous stem cells
Anastasia V. Korel1, Irina I. Kim2, Elena L. Strokova1, Natalia Yu. Pakhomova1, Arkady F. Gusev1, Alla M. Zaydman1
1Novosibirsk Research Institute of Traumatology and Orthopedics n.a. Ya.L. Tsivyan, Novosibirsk, Russia akorel@niito.ru 2Research Institute of
Clinical and Experimental Lymphology - Branch of Federal Research Center
Institute of Cytology and Genetics of SB RAS, Novosibirsk, Russia kii5@yandex.ru
Keywords: infrapatellar (Hoffa’s) fat pad, adipose tissue, CD markers, differentiation, mesenchymal stem cells
Abstract
Stem cells are the basis
for the creation of tissue-engineered structures in regenerative
medicine. The most well-studied sources of stem cells are the embryo and
bone marrow. The use of embryonic cells is associated with ethical
problems, and the collection of bone marrow is accompanied by invasive
procedures. Using adipose tissue as a source of stem cells avoids these
problems. But the collection of adipose tissue requires additional
interventions, which does not exclude the occurrence of cosmetic
defects. Aim of the study was to investigate the possibility of using
mesenchymal stem cells (MSCs) isolated from the infrapatellar (Hoffa’s)
fat pad. Material and methods. As a source of MSCs, tissue samples of
Hoffa’s fat pad removed during the operation were used (8 cases), as a
control - MSCs isolated from human adipose tissue (6 cases). MSCs were
isolated using an enzymatic method. At the 3rd passage, phenotyping with
specific antibodies against CD34, CD45, CD73, CD90, CD105 was performed
by flow cytometry. Differentiation in the chondro- and osteogenic
direction was carried out at the 3rd passage with the appropriate
differentiation media. Chondrogenic differentiation was confirmed by
staining with alcian blue, osteogenic - staining according to von Kossa.
Results and discussion. Statistically significant decrease in CD105
expression, increase in CD73, CD34 expression and lack of adequate
differentiation under standard conditions of differentiation media by
MSCs isolated from the Hoffa’s fat pad compared to control was found.
The data obtained indicate a discrepancy between the cells isolated from
the Hoffa’s fat pad and the requirements for MSCs. Conclusion. The
infrapatellar (Hoffa’s) fat pad cannot be used as a source of
standardized MSCs.
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