Apoptosis is an obstacle to the differentiation of adipose-derived stromal cells into astrocytes

Xiaodong Yuan, Qiaoyu Sun, Ya Ou, Shujuan Wang, Wenli Zhang, Hongliang Deng, Xiaoying Wu, Lili Zhang

1 Department of Neurology, Kailuan General Hospital, Hebei United University, Tangshan, Hebei Province, China

2 Department of Electron Microscopy, Hebei United University, Tangshan, Hebei Province, China

Apoptosis is an obstacle to the differentiation of adipose-derived stromal cells into astrocytes

Xiaodong Yuan1, Qiaoyu Sun1, Ya Ou1, Shujuan Wang1, Wenli Zhang2, Hongliang Deng1, Xiaoying Wu1, Lili Zhang1

1 Department of Neurology, Kailuan General Hospital, Hebei United University, Tangshan, Hebei Province, China

2 Department of Electron Microscopy, Hebei United University, Tangshan, Hebei Province, China

Xiaodong Yuan, Department of

Neurology, Kailuan General Hospital, Hebei United University, Tangshan

063000, Hebei Province, China,

yxd68@sohu.com.

Previous studies have demonstrated that nerve cells differentiated from adipose-derived stromal cells after chemical induction have reduced viability; however, the underlying mechanisms remained unclear. In this study, we induced the differentiation of adult adipose-derived stromal cells into astrocytes using chemical induction. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and flow cytometry showed that, with increasing induction time, the apoptotic rate gradually increased, and the number of living cells gradually decreased. Immunohistochemical staining demonstrated that the number of glial fibrillary acidic protein-, caspase-3- and caspase-9-positive cells gradually increased with increasing induction time. Transmission electron microscopy revealed typical signs of apoptosis after differentiation. Taken together, our results indicate that caspase-dependent apoptosis is an obstacle to the differentiation of adipose-derived stromal cells into astrocytes. Inhibiting apoptosis may be an important strategy for increasing the ef fi ciency of induction.

nerve regeneration; adult adipose-derived stromal cells; cell apoptosis; caspase-dependent apoptosis; cell differentiation; astrocytes; caspase-9; caspase-3; neural regeneration

Yuan XD, Sun QY, Ou Y, Wang SJ, Zhang WL, Deng HL, Wu XY, Zhang LL. Apoptosis is an obstacle to the differentiation of adipose-derived stromal cells into astrocytes. Neural Regen Res. 2014;9(8)：837-844.

Introduction

Adipose-derived stromal cells are stem cells with multidirectional differentiation potential, and have numerous advantages, including strong proliferative ability, low immunogenicity and no legal or ethical issues (Zuk et al., 2001, 2002; McIntosh et al., 2006; Liu et al., 2007; Wu et al., 2013; Cao et al., 2014). Previous studies have shown that adult adipose-derived stromal cells can be successfully transformed into neurons and astrocytes (Safford et al., 2002; Ashjian et al., 2003; Yoshimura et al., 2007; Liu et al., 2010; Ye et al., 2010; Ou et al., 2011a, b). Astrocytes participate in various physiological process and brain development, and help maintain a stable environment for neurons. They also play a very important role in repair and regeneration after brain injury and neurodegeneration (Pekny and Nilsson, 2005; Jacobsen et al., 2006; Di Giorgio et al., 2007; Holden, 2007; Van Den Bosch and Robberecht, 2008). The in vitro induction of these astroglia has provided a new way for the treatment of clinical nervous system damage and neurodegenerative disorder (Kang et al., 2003; Goldman, 2005; Nakagami et al., 2006). However, when 3-isobutyl-1-methylxanthine was used to induce adipose-derived stromal cell differentiation, the survival time of the resulting astrocytes was only approximately 30 days (Liu et al., 2010; Ou et al., 2011b), limiting further research and clinical applications.

Our previous experiments showed that apoptosis is a major cause of death of neurons originating from adipose-derived stromal cells (Cai et al., 2011; Lu et al., 2012). Studies have shown that there are two types of apoptosis; caspase-dependent and caspase-independent (Daniel, 2000; Vittar et al., 2010; Zhang et al., 2011). In caspase-dependent apoptosis, the caspase family of proteases mediates apoptosis (Gil and Esteban, 2000; Chen and Wang, 2002; Kavitha et al., 2012). The caspases include two types of caspases (Ren et al., 2012; Tatsuta et al., 2013); initiators, such as caspase-9, which cleave and activate other caspases (von Roretz et al., 2013), and effectors, such as caspase-3, which cleave various substrates and decompose cell structure or inactivate enzymes (Kang et al., 2010; Wirawan et al., 2010). As an “executioner”protease, caspase-3 plays an important role in apoptosis (Compton and Cidlowski, 1986; Adrain et al., 2001; Slee et al., 2001). Previous studies have shown that caspase-dependent apoptosis occurs during adipose-derived stromal cell differentiation into neurons (Lu et al., 2012). Therefore, in this study, we investigated caspase-dependent apoptosis during adipose-derived stromal cell differentiation into astrocytes.

Materials and Methods

Extraction and culture of adult adipose-derived stromal cells

Figure 1 Changes in cell morphology before and after ADSC induction (inverted phase contrast microscope).

Figure 3 Positive expression rate of glial fi brillary acidic protein (GFAP), caspase-3 and caspase-9 in adult adipose-derived stromal cells differentiated at different time points (immunocytochemistry).

Figure 4 Survival rate of adult adipose-derived stromal cells differentiated at different time points assessed with MTT.

Volunteers were 13 healthy adults, aged 20-35 years, from the Physical Check-up Center, Kailuan General Hospital, Tangshan, Hebei Province, China. Needle aspiration was used to extract abdominal subcutaneous adipose tissue of adult volunteers without endocrine or hematological diseases. 10-30 mL adipose tissue was collected each time. Written informed consent from the volunteers was obtained. The protocol was approved by the Medical Ethics Committee of Kailuan General Hospital of Hebei United University, China.

Figure 2 Expression of GFAP, caspase-3 and caspase-9 at various time points after adipose-derived stromal cells differentiation (immunocytochemical staining, inverted phase contrast microscope, × 200).

Based on the method of Ye et al. (2010) and other experimental protocols, 0.1% collagenase type I (Solarbio, Beijing, China) was added, and the tissue was placed in a 37°C water bath for digestion for 1 hour and then centrifuged at 1,000 r/min for 5 minutes. Supernatant was aspirated out. The undigested tissues and the underlying cells were stirred to mix, and then fi ltered through a 100-mesh sieve. The samples were centrifuged at 1,000 r/min for 5 minutes, and the supernatant was removed. The remaining cell pellet was seeded into culture fl asks at a density of 8 × 103/cm2and placed in a 37°C, 5% CO2humidified incubator. The culture medium was replaced after 48 hours to remove residual erythrocytes and non-adherent impurities. The culture medium was replaced every 2-3 days. About 10-14 days after the cells reached 90% con fl uence, trypsin-ethylenediaminetetraacetic acid was used for digestion, and cells were passaged at a 1:2 ratio. Morphological changes in cells were observed using an inverted phase contrast microscope (Olympus, Tokyo, Japan).

Adult adipose-derived stromal cell differentiation into astrocytes

Passage 3-6 adipose-derived stromal cells, in good condition, were digested with trypsin-ethylenediaminetetraacetic acid and slides were prepared. When the cells reached 70-80% con fl uence, the medium was removed, inducer was added, and morphological changes were observed after 48 hours and 7, 14 and 21 days under the inverted phase contrast microscope. Inducer components: 0.5 mmol/L 3-isobutyl-1-methylxanthine (Sigma, St. Louis, MO, USA), 1 μmol/L dexamethasone, 10 μmol/L insulin, 200 μmol/L indomethacin, 10 mmol/L hydroxyethyl piperazine ethanesulfonic acid (Hyclone, Logan, UT, USA), 2 mmol/L glutamine, 1% non-essential amino acids, 0.5% absolute ethyl alcohol, 10% fetal bovine serum (Hyclone), 100 U/mL penicillin and 100 μg/mL streptomycin, and 85% high-glucose Dulbecco’s modi fi ed Eagle’s medium (DMEM) (Hyclone).

Glial fi brillary acidic protein, caspase-3 and caspase-9 expression in the induced cells

At 48 hours, and 7, 14 and 21 days after induction, cells were fi xed in 4% paraformaldehyde for 30 minutes, permeabilized using 0.1% TritonX-100 for 8 minutes, and incubated with 3% H2O2for 10 minutes. Cells were then incubated in working solutions of primary antibodies-rabbit anti-human glial fi brillary acidic protein (1:100; Beijing Biosynthesis Biotechnology, Beijing, China), caspase-9 (1:100; Beijing Biosynthesis Biotechnology) and rabbit anti-human caspase-3 monoclonal (1:100; Boster, Wuhan, Hubei Province, China) at 4°C overnight, and then with goat anti-rabbit IgG-horseradish peroxidase (1:50; Beijing Zhongshan Goldbridge, Beijing, China) for 30 minutes at 37°C. Labeling was visualized with 3,3′-diaminobenzidine (Beijing Zhongshan Golden BridgeBiotechnology), and cells were then stained with hematoxylin. Immunoreactive cells were counted at high magni fi cation (× 100). Five fields were quantified per sample. Three samples in each group were observed under the inverted phase contrast microscope.

3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay for cell viability after induction

Adipose-derived stromal cells at passages 3-6 were digested and seeded onto 12-well culture plates, and inoculated at a density of 1 × 105cells/well. At 48 hours, and 7, 14 and 21 days after induction, cells in each well were incubated with 5 mg/mL MTT (Sigma), 100 μL, at 37°C for 4 hours. The liquid in the well was discarded, and 1,000 μL dimethyl sulfoxide was added to each well. The plates were then agitated at a low speed of 1,000 r/min for 15 minutes. 100 μL aliquots of the solutions were transferred to a 96-well plate and the absorbance at 490 nm was measured using a microplate reader (Thermo Scientific, Pittsburgh, PA, USA). The absorbance is directly proportional to the number of living cells (Wyllie, 1980). Each experiment was repeated fi ve times.

Quanti fi cation of early apoptotic cells by fl ow cytometry

The cells induced for 48 hours, and 7, 14 and 21 days were digested and collected. A single cell suspension was prepared at a concentration of 1 × 106/mL and centrifuged at 1,000 r/min for 5 minutes. The supernatant was discarded, and then 190 μL buffer (Invitrogen, Carlsbad, CA, USA) and 10 μL PI dye solution (Invitrogen) were added. The samples were protected from light and quanti fi ed by fl ow cytometry (BD FACSCalibur, San Jose, CA, USA) within 1 hour. Each experiment was repeated three times.

Ultrastructural characteristics of astrocytes and apoptotic cells after induction

The cells induced for 14 days were digested, centrifuged, and fi xed in 3% glutaraldehyde and 1% osmic acid, followed by propionaldehyde dehydration and epoxy resin embedding. Cells were sliced using a microtome (Abnova, Walnut, CA, USA) and stained with 2% uranyl acetate and lead citrate. The ultrastructure of cells was observed and photographed with a transmission electron microscope (H7650, Hitachi, Tokyo, Japan).

Statistical analysis

All experimental data were analyzed using SPSS 13.0 (SPSS, Chicago, IL, USA). Measurement data were expressed as mean ± SD. Intragroup differences were compared using one-way analysis of variance followed by Student-Newman-Keuls test. Values of P ＜ 0.05 were considered statistically signi fi cant.

Results

Morphological changes in cells differentiated from adipose-derived stromal cells

Primary cultured adipose-derived stromal cells adhered at 24 hours, and were observed under the inverted phase contrast microscope. Cells had a triangular and short fusiform appearance (Figure 1A). After 48 hours of culture, the cells had a long fusiform shape, similar to that of the fi broblasts. At 7-10 days, a large number of long spindle-shaped cells were arranged in a whorl pattern (Figure 1B). When passaged to the third generation, adipose-derived stromal cells were almost fusiform. At 24 hours after induction, the cytoplasm retracted to the nucleus (Figure 1C). At 48 hours after induction, round, polygonal or irregular-shaped cells were surrounded by a halo. Parts of cell bodies stretched out slender processes and multiple branches. The cytoplasm was uniform, the nucleus was oval or round, and nucleoli were visible. At 7 days after induction, some of the cells showed the shape of typical astrocytes. Simultaneously, cell protrusions were more extensive, slender branches increased in number and displayed a reticular appearance. The cytoplasm was uniform, the nucleus was large, oval or round, and more biased towards one side of the cell body. Nucleoli were clearly visible (Figure 1D). At 14 days after induction (Figure 1E), cell morphology showed no signi fi cant changes from that at 7 days. At 21 days after induction, the number of cells was significantly reduced (Figure 1F). Cells were triangular or irregularly shaped, and cell protrusions were shorter and less numerous than at 14 days of induction. The nucleus showed no signi fi cant changes compared with day 14.

Expression of glial fi brillary acidic protein, caspase-3 and caspase-9 during adipose-derived stromal cell differentiation

At 48 hours of induction, glial fi brillary acidic protein expression was observed in a part of the cytoplasm by immunocytochemical staining. The number of glial fi brillary acidic protein-positive cells gradually increased (P ＜ 0.05), and peaked at 14 days. At 21 days, there was no signi fi cant difference in the number of glial fi brillary acidic protein-positive cells compared with 14 days (P ＞ 0.05). Expression of caspase-3 and caspase-9 was mainly observed in the cytoplasm. The number of caspase-3- and caspase-9-positive cells gradually increased over the induction period (P ＜ 0.05; Figures 2, 3).

Cell survival after adult adipose-derived stromal cell differentiation

MTT assay showed that the survival rate of cells gradually decreased over time: at 48 hours, and 7, 14 and 21 days of induction (P ＜ 0.05; Figure 4).

Early apoptosis after adult adipose-derived stromal cell differentiation

Flow cytometry revealed that at 48 hours, and 7, 14 and 21 days after induction, the apoptotic rate was 4.43 ± 0.26%, 7.80 ± 0.53%, 11.93 ± 0.34% and 14.72 ± 0.43%, respectively. The apoptotic rate gradually increased over time: at 48 hours, and 7, 14 and 21 days (P ＜ 0.05; Figure 5).

Apoptosis and ultrastructural features of astrocytes differentiated from adipose-derived stromal cells

Under the transmission electron microscope, at 14 days after differentiation, the cell bodies of astrocytes were roundor oval. The membrane surface was not smooth, and there were numerous processes. There were varying amounts of bundles of fibers, endoplasmic reticulum, lysosomes and mitochondria in the cytoplasm. Mitochondrial volume was large, and nuclei were oval or irregularly shaped, having 1 or 2 nucleoli, more euchromatin, and reduced and dispersed heterochromatin. The cell bodies of apoptotic astrocytes narrowed, processes from the cell membrane were noticeably decreased or missing, and the surface was smooth. In the cytoplasm, mitochondria exhibited swelling, volume was increased, and the cristae were ruptured and vacuolated. Nuclei were irregular; the nuclear membranes were wrinkled and retracted or even showed karyolysis. Chromatin was reduced, but the amount of heterochromatin was increased. The nuclear chromatin was condensed, and often accumulated near the edges of the nuclear membrane, with blocky or crescent-shaped bodies (Figure 6).

Discussion

Numerous studies have shown that adipose-derived stromal cells can successfully differentiate into astrocytes in vitro (Safford et al., 2002; Ashjian et al., 2003; Liu et al., 2010; Ou et al., 2011b). The induced cells have the typical morphology of astrocytes and express specific markers, and have a characteristic ultrastructure and electrophysiological properties (Ou et al., 2011a). However, our previous experiments showed that many cells died during adipose-derived stromal cell differentiation, and the number of viable cells decreased with increasing length of induction (Liu et al., 2010; Ou et al., 2011b), thereby limiting further research and hindering the application of astrocytes differentiated from adipose-derived stromal cells. Indeed, in the present study, although the expression rate of glial fi brillary acidic protein, the speci fi c marker of astrocytes, reached a peak of 79.2% at 14 days, the number of viable cells had decreased. Therefore, it is necessary to perform further research on the mechanisms of cell death during the differentiation of adipose-derived stromal cells into astrocytes, and to optimize cell differentiation protocols to improve the survival rate of astrocytes differentiated from adipose-derived stromal cells.

Apoptosis is a process of programmed cell death (Wyllie, 1980; Johansson et al., 2010; Giansanti et al., 2011; Freire, 2012; Igder et al., 2013; Tognon et al., 2013). Our previous studies showed that apoptosis is a major cause of the death of neurons differentiated from adipose-derived stromal cells (Cai et al., 2011; Lu et al., 2012). As the preferred method for early detection of apoptotic cells, Annexin V/PI double-staining and fl ow cytometry can be used to analyze early apoptotic cells ef fi ciently (Nicoletti et al., 1991; Grebeňová et al., 2004; Samsel et al., 2004; Suárez et al., 2004; Guo et al., 2011; Wlodkowic et al., 2013). Therefore, we studied cell death rate in the early stage by fl ow cytometry. The results demonstrated that the death rate increased over time, peaking at 21 days of induction. This further con fi rmed that apoptosis is a major cause of cell death.

Apoptosis includes caspase-dependent apoptosis and caspase-independent apoptosis (Liu et al., 2013). In caspase-dependent apoptosis, the caspase family is a key mediator of cell death. As the preferred method for detecting apoptosis (Zhou et al., 2012), transmission electron microscopy plays a crucial role in its detection (Ji et al., 2011; Würstle et al., 2012). Our fi ndings revealed that caspase-dependent apoptosis is a major apoptotic pathway during cell differentiation. Furthermore, the numbers of caspase-9- and caspase-3-positive cells increased over time and were associated with apoptosis of astrocytes differentiated from adipose-derived stromal cells. The expression rate of caspase-9, the main initiation factor of apoptosis (Fombonne et al., 2012; White et al., 2012; Brentnall et al., 2013; Qin et al., 2013), reached 30.27% at 21 days of induction. However, for caspase-3, the rate was 46.47%, signi fi cantly higher than that for caspase-9, suggesting a significant amplification effect. For both caspase-3 and caspase-9, expression is mainly in the cytoplasm, especially around the nucleus; however, there is no signi fi cant expression in the protrusions of the induced cells. The expression of caspase-9 was less than the expression of executioner caspase-3, suggesting an amplification effect in the process of induction.

During the differentiation of adipose-derived stromal cells into astrocytes, expression of glial fi brillary acidic protein, an important marker of astrocytes (Bernal and Peterson, 2011; Sokolowski et al., 2011; Yeh et al., 2011; Sukumari-Ramesh et al., 2012; Hoppe et al., 2013), is evenly detected in the cytoplasm as well as in the protrusions. Glial fi brillary acidic protein bundles are evenly distributed in the cytoplasm as well as in the cell processes of normal astrocytes differentiated from adipose-derived stromal cells. More organelles are observed, including mitochondria, endoplasmic reticulum and lysosomes. There is more euchromatin and less heterochromatin in nuclei, and the heterochromatin is dispersed. In contrast, in the cytoplasm of apoptotic cells, the mitochondria, concentrated around the nuclei, were signi fi cantly swollen, the cristae were ruptured, and vacuolization was observed. The membranes of nuclei were wrinkled, and some were fragmented. The chromatin was condensed and distributed at the membrane, with a block or crescent shape, typical of apoptosis. Finally, cell morphological changes, including shrinkage, and a decrease or even disappearance of protrusions and microvilli occur.

In summary, adipose-derived stromal cells can differentiate into astrocytes using a chemical inducer mainly consisting of 3-isobutyl-1-methylxanthine. The number of living cells decreases over the duration of induction. Caspase-dependent apoptosis is the main pathway of apoptosis during induction.

Acknowledgments:The author would like to thank Yang XL and Bo Y of Cosmetic Plastic Surgery Center from Kailuan General Hospital in China. Constant supports and technical assistance have been offered generously by teachers from the Experimental Center of Hebei United University in China.

Figure 5 Quantitative distribution of early apoptosis of Adipose-derived stromal cells at various time points after differentiation, as detected by fl ow cytometry.

Figure 6 Ultrastructural characteristics of adipose-derived stromal cells-differentiated astrocytes and apoptotic cells at 14 days (transmission electron microscopy).

Author contributions:Yuan XD was responsible for writing the manuscript, study design, concept, implementation and data arrangement. Sun QY, Ou Y and Zhang LL performed the whole experiment. Wang SJ and Deng HL assisted in data collection and analysis. Zhang WL was responsible for images analysis of electron microscopy. Wu XY provided instruments, equipment and reagents. All authors approved the final version of the paper.

Con fl icts of interest:None declared.

Peer review:This study found that caspase-dependent apoptosis is a reason for the death of astrocytes differentiated from adipose-derived stromal cells. The inhibition of this kind of apoptosis may be an important measure to promote the induction effects of astrocytes. This provides a substance basis for treatment and repair of brain injury and neurodegenerative disease using astrocytes.

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Copyedited by Patel B, Frenchman B, Yu J, Qiu Y, Li CH, Song LP, Zhao M

Retraction Notice

The following article from Neural Regeneration Research, ‘Brain-derived neurotrophic factor inhibits glucose intolerance after cerebral ischemia’ by Shu et al., published on Volume 8, Issue 25, Pages 2370-2378 has been retracted by agreement between the authors and the journal. The retraction has been agreed because the figures and corresponding descriptions included in the article is a duplication of the paper by Harada et al. that had already appeared in J Pharmacol Sci, 118, 109-116; 2012.

One of the conditions of submission of a paper for publication is that authors declare explicitly that their work is original and has not been submitted for or appeared in a publication elsewhere. As such this article represents a violation of the journal’s publishing policies.

Reference

Shu XL, Zhang YS, Xu H, Kang K, Cai DL (2013) Brain-derived neurotrophic factor inhibits glucose intolerance after cerebral ischemia. Neural Regen Res 8:2370-2378.

10.4103/1673-5374.131600

http://www.nrronline.org/

Accepted: 2014-03-28