High efficient isolation and systematic identification of human adipose-derived mesenchymal stem cells
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Developing efficient methods to isolate and identify human adipose-derived mesenchymal stem cells (hADSCs) remains to be one of the major challenges in tissue engineering.
We demonstrate here a method by isolating hADSCs from abdominal subcutaneous adipose tissue harvested during caesarian section. The hADSCs were isolated from human adipose tissue by collagenase digestion and adherence to flasks.
The yield reached around 1 × 106 hADSCs per gram adipose tissue. The following comprehensive identification and characterization illustrated pronounced features of mesenchymal stem cells (MSCs). The fibroblast-like hADSCs exhibited typical ultrastructure details for vigorous cell activities. Karyotype mapping showed normal human chromosome. With unique immunophenotypes they were positive for CD29, CD44, CD73, CD105 and CD166, but negative for CD31, CD34, CD45 and HLA-DR. The growth curve and cell cycle analysis revealed high capability for self-renewal and proliferation. Moreover, these cells could be functionally induced into adipocytes, osteoblasts, and endothelial cells in the presence of appropriate conditioned media.
The data presented here suggest that we have developed high efficient isolation and cultivation methods with a systematic strategy for identification and characterization of hADSCs. These techniques will be able to provide safe and stable seeding cells for research and clinical application.
KeywordsMajor Histocompatibility Complex Mesenchymal Stem Cell Human Adipose Tissue Endothelial Differentiation Adipose Tissue Sample
List of abbreviations
adipose-derived mesenchymal stem cells
mesenchymal stem cells
endothelial cell growth medium 2
fluorescein-activated cell sorting
fetal bovine serum
kinase insert domain receptor
low glucose-Dulbecco's modified Eagle's medium
major histocompatibility complex
semi-quantitive reverse transcriptase-polymerase chain reaction
vascular endothelial growth factor-165.
Mesenchymal stem cells have been widely used in experimental and clinical research because of their unique biological characteristics and advantages [1, 2, 3, 4]. In a previous study, we have developed standardized techniques for the isolation, culture, and differentiation of bone marrow-derived mesenchymal stem cells [5, 6, 7]. Recent reports have shown that the widely-spreaded human adipose tissue provides abundant source of mesenchymal stem cells, which can be easily and safely harvested as compared with human bone marrow [8, 9, 10]. The adipose tissue from abdominal surgery or liposuction is usually rich in stem cells which can meet the needs of cell transplantation and tissue engineering . Meanwhile, these stem cells have high ability for proliferation and multilineage differentiation [12, 13]. Therefore, human adipose-derived mesenchymal stem cell (hADSC) is becoming a potential source for stem cell bank and an ideal source of seeding cells for tissue engineering. Although some labs have successfully isolated hADSCs from adipose tissues, there is still no any widely-accepted efficient method for isolating and culturing highly homogenous and undifferentiated hADSCs. The comprehensive methods for identification and characterization of hADSCs have not been fully established yet. The aim of current study was to develop high efficient methods to isolate and identify hADSCs.
Human adipose tissue was obtained at caesarian section from the abdominal subcutaneous tissue of obese women delivered, in the maternity department at Jilin University (age range: 23-41 years; mean = 32 years old). The subjects were healthy without any regular medication. Informed consent was obtained from the subjects before the surgical procedure. The study protocol was approved by the Ethic Committee of Jilin University. After being removed, ~5 g adipose tissue sample is relocated in a sterilized bottle filled with 0.1 M phosphate-buffered saline (PBS) at 4°C within 24 h prior to use.
Isolation of hADSCs and Cell Culture
The procedure followed the description by Zuk et al.  with some modifications. The adipose tissue sample was extensively washed with sterile PBS containing 1000 U/ml penicillin and 1000 μg/ml streptomycin to remove contaminating blood cells. The specimen was then cut carefully. Connective tissue and blood vessels were removed and the tissue was cut into 1 mm3 pieces. The extracellular matrix was digested with 0.1% collagenase Type I (Invitrogen, USA) at 37°C, and shaken vigorously for 60 min to separate the stromal cells from primary adipocytes. The collagenase Type I activity was then neutralized by adding an equal volume of Low glucose-Dulbecco's modified Eagle's medium (L-DMEM, Hyclone, USA) containing 10% fetal bovine serum (FBS, Invitrogen, USA). Dissociated tissue was filtered to remove debris, and centrifuged at 1500 rpm for 10 min. The suspending portion containing lipid droplets was discarded and the cell pellet was resuspended and washed twice. Contaminating erythrocytes were lysed with an osmotic buffer, and the remaining cells were plated onto 6-well plate at a density of 1 × 106/ml. Plating and expansion medium consisted of L-DMEM with 10% FBS, 100 U/ml penicillin, and 100 mg/L streptomycin. Cultures were maintained at 37°C with 5% CO2. The medium was replaced after 48 hours, and then every 3 days. Once the adherent cells were more than 80% confluent, they were detached with 0.25% trypsin-0.02% EDTA, and re-plated at a dilution of 1:3.
Transmission Electron Microscopy
1 × 107 hADSCs or endothelial differentiated hADSCs were washed twice in 0.1 M PBS, and then were centrifuged at 1500 rpm for 10 min. The pellet was pre-fixed in 4% glutaraldehyde at 4°C overnight, then post-fixed in 1% osmium tetroxide at 4°C for 60 min and further dehydrated in acetone and embedded in epoxy resin. Conventional ultrathin sections were prepared in Uranyl acetate. After double-stained in lead citrate, they were observed and photographed under transmission electron microscope (JEM-1200EX) (JEOL Ltd., USA).
G-banding karyotype analysis
To analyze the karyotype of hADSCs within 12 passages, cell division was blocked in mitotic metaphase by 0.1 μg/ml colcemid for 2 h. Then the cells were trypsinized, resuspended in 0.075 M KCl solution, and incubated for 30 min at 37°C. The cells were fixed with methanol and acetic acid mixed by 3:1 ratio. G-band standard staining was used to observe the chromosome. Karyotypes were analyzed and reported according to the International System for Human Cytogenetic Nomenclature.
2 × 105 hADSCs were incubated with primary antibodies against human CD29, CD45, CD73, CD105, CD166, HLA-DR (Biolegend, USA) and CD31, CD34, CD44 (BD Biosciences, USA). All antibodies were diluted 1:100 and incubated with cells for 30 min at room temperature. We used same-species, same-isotype irrelevant antibody as negative control. The cells were then washed twice in PBS and incubated with fluorescein isothiocyanate (FITC)-conjugated secondary antibodies (1:50 dilution) for 30 min at 4°C. After two washing steps, cells were resuspended in 300 μl PBS for flow cytometric analysis and analyzed by fluorescein-activated cell sorting (FACS) Calibur (BD Biosciences, USA).
Indirect Immunofluorescence assay
All hADSCs were processed as described previously . Monoclonal antibodies against specific CD markers and lineage-specific proteins were used. The fluorescence signals were detected by laser scanning confocal microscope (Olympus FV500, Japan).
Analysis of growth kinetics and cell cycle
Using cell counting, we analyzed the proliferative capacity of hADSCs from different passages. The cells were seeded onto 24-well culture plates with 5 × 103 cells per well and counted daily by trypan blue exclusion for one week and cell growth curves were recorded. The cell population doubling time (DT) of hADSCs was calculated with the Patterson formula . For cell cycle anaysis, 1 × 107cells were collected, fixed for 20 min at 4°C in 70% ethanol, and stained with 50 μg/ml propidium iodide (PI) at 4°C for 30 min. DNA content was analyzed by FACS Calibur using Cell Quest software (BD Biosciences, USA) in 24 h. Under these conditions, quiescent cells (G0/G1) were characterized by the minimal RNA content and uniform DNA content. The results of the study were expressed as mean ± standard error, and statistical comparisons were made using the two-sided Student's t-test.
Once culture-expanded cells reached ~80% confluent, they were cultured in adipogenic medium for 2 weeks. The medium consisted of L-DMEM supplemented with 10% FBS, 1 μmol/L dexamethasone, 50 μmol/L indomethacin, 0.5 mM 3-isobutyl-1-methyl-xanthine and 10 μM insulin. At the end of the culture, the cells were fixed in 4% Paraformaldehyde for 20 min and stained with Oil red-O solution to show lipid droplets in induced cells [5, 13, 15]. To quantify retention of Oil red O, stained adipocytes were extracted with 4% Igepal CA630 (Sigma-Aldrich, USA) in isopropanol for 15 min, and absorbance was measured by spectrophotometry at 520 nm.
The hADSCs were induced for 4 weeks in osteogenic medium containing L-DMEM, 10% FBS, 0.1 μM dexamethasone, 200 μM ascorbic acid, 10 mM β-glycerol phosphate . After induction, osteoblasts were confirmed by cytochemical staining with alkaline phosphatase (ALP) to detect the alkaline phosphatase activity, and then were stained with 40 mM Alizarin Red S dye (pH 4.2) to detect mineralized matrix according to the protocol described previously [16, 17]. Phosphatase Substrate Kit (Pierce, IL, USA) containing PNPP (p-nitrophenyl phosphate disodium salt) was used to quantify the ALP activity in cell cultures. PNPP solution was prepared by dissolving two PNPP tablets in 8 ml of distilled water and 2 ml of diethanolamine substrate buffer. Cells were plated at 5000 per well in 96 well plates and cultured in OBM for 2 weeks. After washing twice with PBS, cells were incubated with 100 μl/well PNPP solution at room temperature for 30 min. 50 μl of 2 N NaOH was added to each well to stop the reaction. Non-cell plated wells treated by the same procedure were used as blank control. The absorbance was measured at 405 nm in a kinetics ELISA reader (Spectra MAX 250, Molecular Devices, CA, USA).
Osteogenic or adipogenic specific marker-osteopontin (OPN) or PPARγ-2 gene expression was detected by semi-quantitative reverse transcriptase-polymerase chain reaction (sqRT-PCR). Total RNA was extracted from uninduced hADSCs and induced hADSCs with Trizol reagent (Invitrogen, USA). Using total RNA as template, reverse transcription reactions were carried out with oligo dT-adaptor primer. Then semi-quantitative PCR amplification was performed for human OPN and PPARγ-2. The primers used are listed below: OPN specific primers, 5'-CCAAGTAAGTCCAACGAAAG-3' and 5'-GGTGATGTCCTCGTCTGTA-3'; PPARγ-2 specific primers, 5'-CATTCTGGCCCACCAACTT-3' and 5'-CCTTGCATCCTTCACAAGCA-3'; β-actin specific primers, 5'-CATGTACGTTGCTATCCAGGC-3' and 5'-CTCCTTAATGTCACGCACGAT-3'. PCR cycles were as follows: 94°C for 2 minutes, (94°C for 30 seconds, 55°C for 30 seconds, 72°C for 1 minute) × 35 cycles, 72°C for 5 minutes. The PCR products were analyzed by electrophoresis on 1.5% agarose gel and image acquisition and data analysis were accomplished with Digital Gel Image System (Tanon, China).
Endothelial differentiation and immunocytochemical analysis
Endothelial differentiation was induced as described previously with some modifications [18, 19, 20]. A 24-well cell culture plate was coated with fibronectin (FN) (5 μg/cm2) (BD Bioscience, USA) in each well. 1 × 104 hADSCs were seeded in plates and incubated for up to 15 days in endothelial differentiation medium containing endothelial growth medium (EGM2-MV) (Lonza, USA) supplemented with 50 ng/mL vascular endothelial growth factor-165 (VEGF165) (PeproTech, USA), 100 U/mL penicillin, and 100 μg/mL streptomycin. 15 days after endothelial differentiation started, the cells were fixed with 4% paraformaldehyde for 10 min at room temperature, and rinsed with PBS. The fixed cells were then incubated for 1 hour at 37°C with mouse antibodies against human CD31 or CD34 (BD Bioscience, USA), KDR (NeoMarker, USA) at 1:500 dilution. After incubation in a blocking solution containing 1% normal goat serum, they were incubated with secondary antibodies. A streptavidin-biotin peroxidase detection system was used to detect antibody binding.
Isolation method gave high yield of hADSCs with normal morphological characters
Under the transmission electron microscope, most of the hADSCs showed irregular morphology of nuclear located at one side of the cell, and the cytoplasm contained numerous mitochondria and rough endoplasmic reticulums (Figure 1C). Abundant microvilli extended from cell surface into the cytoplasm and formed inclusion body-like structures (Figure 1D).
Karyotypes of two hADSC cultures were analyzed and reported according to the International System for Human Cytogenetic Nomenclature. Both results showed normal female chromosome type (46, XX) with no chromosome abnormalities observed (Figure 1E).
The cells from different passages expressed same MSC-specific markers
After indirect immunofluorescent staining, hADSCs were observed by laser confocal scanning microscope. Cells that were assayed with monoclonal antibodies against the 6 MSC-specific markers showed green fluorescence, which confirmed the results above (Figure 2C).
Growth kinetics indicated high capacity of proliferation
The hADSCs had good mutilineage differentiate potential
Seeding cell is one of the key elements in tissue engineering. Recent reports have shown that hADSCs can be easily harvested from adipose tissue without ethical concern or problems of transplant rejection, and these cells have high proliferation rates for in vitro expansion with multilineage differentiation capacity [8, 9, 10, 11, 12, 13]. Because of these favorable characteristics, there is considerable interest in the applications of hADSCs. Since Rodbell first isolated preadipocytes from adipose tissue  a variety of methods have been developed, but the purity of isolated hADSCs is not high and the methods for identification have not been fully developed. Therefore, developing high efficient methods to isolate and identify hADSCs would be very valuable.
As demonstrated in the present manuscript we have established a simple and effective way to obtain high-purity hADSCs by using collagenase digestion and adherence screening. Isolated hADSCs proliferated at a high rate and maintained a multipotentdifferentiation capacity in vitro for up to 12 passages.
Since no unique molecular marker for mesenchymal stem cells has been established we used multiple surface markers for hADSCs identification. Mesenchymal stem cells bind to extracellular matrix through surface antigens which involve in cell-cell and cell-matrix interactions , we therefore selected adhesion molecules, including CD44, CD166, CD29 (a member of the integrin family), and mesenchymal markers (such as CD73 and CD105). The results showed that the positive staining rate was 95% or more, and the hematopoietic/leukocytic/endothelial markers such as CD31, CD34, CD45 and the major histocompatibility complex (MHC) class II (HLA-DR) were negative. These data not only excluded endothelial cell contamination, but also suggested that the clinical application of hADSCs can bypass MHC restriction. Consequently they were suitable for allograft procedures, consistent with the report of Aust . In addition, the phenotypes of hADSCs showed no significant difference between different passages, indicating that the cells can be stably amplified in vitro for several passages. Ultrastructural imaging suggested that hADSCs were quite active with high capacity of protein synthesis and nutrients uptake as reported before . Most cells were in resting period of cell cycle agreeing with the characteristics of human bone marrow-derived mesenchymal stem cells . The doubling time was also consistent with stem cell characteristic, namely, a high degree of proliferation. No chromosomal abnormalities were observed in hADSCs of passage 12, providing an experimental basis for the safely clinical application of these cells. Furthermore, our studies showed that hADSCs could differentiate into osteoblasts, adipocytes and endothelia, which are typical mesenchymal stem cell characteristics.
Taken together, this study developed an efficient method for isolation and cultivation of a large amount of hADSCs. It also established a systemic and comprehensive strategy to identify and characterize these cells. These data will significantly contribute to tissue engineering by providing abundant seeding cells with high quality.
This study was supported by a grant from the National 863 Program (No. 2004AA205020) and the National Natural Science Foundation of China (No. 30700872). We sincerely thank Dr. William Orr (Professor, Department of Pathology, University of Manitoba, Canada) for facilitating preparation of this manuscript.
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