Exp Neurobiol 2013; 22(4): 283-300
Published online December 30, 2013
© The Korean Society for Brain and Neural Sciences
Hyo Eun Moon1,2,3, Seung Hee Yoon5, Yong Suk Hur6, Hyung Woo Park1,2,3, Ji Young Ha5, Kyung-Hee Kim5, Jung Hee Shim5, Seung Hyun Yoo6, Jin H. Son5, Seung Leal Paek1,2,3,8, In Keyoung Kim1, Jae Ha Hwang1, Dong Gyu Kim1, Han-Joon Kim4, Beom Seok Jeon4, Sung Sup Park7 and Sun Ha Paek1,2,3*
1Department of Neurosurgery, 2Cancer Research Institute, 3Ischemic/Hypoxic Disease Institute, Seoul National University College of Medicine, 4Department of Neurology, Seoul National University College of Medicine, Seoul 110-744, 5Department of Brain & Cognitive Sciences, College of Pharmacy, Brain Disease Research Institute, Ewha Woman’s University, Seoul 120-750, 6Department of Biochemistry, Inha University School of Medicine, Incheon 402-751, 7Department of Laboratory Medicine, Seoul National University Hospital, Seoul 110-744, Korea, 8Department of Neurosurgery, Mayo Clinic, USA
Correspondence to: *To whom correspondence should be addressed.
TEL: 82-2-2072-3993, FAX: 82-2-744-8459
Mitochondrial dysfunction in dopaminergic neurons of patients with idiopathic and familial Parkinson's disease (PD) is well known although the underlying mechanism is not clear. We established a homogeneous population of human adipose tissue-derived mesenchymal stromal cells (hAD-MSCs) from human adult patients with early-onset hereditary familial Parkin-defect PD as well as late-onset idiopathic PD by immortalizing cells with the hTERT gene to better understand the underlying mechanism of PD. The hAD-MSCs from patients with idiopathic PD were designated as "
Keywords: hTERT, hAD-MSC, immortalization, Parkinson’s disease, diagnosis
Parkinson's disease (PD) is characterized by the selective loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNpc) as well as by complex interactions between susceptible genes and various environmental risk factors [1-3]. Aberrant mitochondrial forms and functions are widely accepted pathogenic mechanisms in a subset of people with PD [2, 3]. Mitochondrial dysfunction in the dopaminergic neurons of idiopathic and familial PD is well known although the underlying mechanisms are not clear. The most direct evidence for disrupted mitochondrial metabolism has come from studies using autopsy tissues and other tissue samples and from
Multipotent mesenchymal stromal cells (MSC) from human adipose tissue represent an excellent source of progenitor cells for cell therapy and tissue engineering [17, 18]. Human adipose tissue is a rich source of MSC providing an abundant and accessible source of adult stem cells. Here, we isolated human adipose tissue-derived mesenchymal stromal cells (hAD-MSCs) from patients with idiopathic PD designated as "
In culture, normal human cells have a finite lifespan ultimately ceasing to proliferate in a process called replicative senescence . Telomeres are specific structures found at the ends of chromosomes in eukaryotes, which protect the chromosome ends . Telomerase is a ribonucleoprotein that synthesizes and directs the telomeric repeats onto the 3' end of existing telomeres using its RNA component as a template . Human telomerase reverse transcriptase (hTERT) is the catalytic component of a functional telomerase complex, which is important in maintaining cell immortality. In humans, telomere shortening limits the proliferative potential of somatic cells, and the introduction of hTERT is a valuable method that circumvents the attenuated mitotic competence of somatic cells associated with TERT inactivation .
In the present study, for the first time, to overcome the cellular senescence of primary cultured AD-MSCs from PD patients, we established hTERT-immortalized wild type, idiopathic and Parkin-defect mesenchymal stromal cell lines isolated from the adipose tissues of PD patients. Then, we used these immortalized cell lines to investigate mitochondrial abnormalities in the idiopathic and Parkin-defect PD cell lines compared to the wild type cell line. This study suggests that the hTERT-immortalized hAD-MSC cell lines established from patients with idiopathic and familial Parkin-defect PD could be good cellular models to evaluate mitochondrial dysfunction to better understand the pathogenesis of PD and to develop early diagnostic markers and effective therapy targets for the treatment of PD.
This study was approved by the institutional review board of the Biomedical Research Institute of Seoul National University Hospital (IRB No. 0707-024-212). Written informed consent was obtained from the patients. Subcutaneous adipose tissue was acquired during the Deep Brain Stimulation (DBS) surgery performed in patients with idiopathic and Parkin-defect PD and compared with non-PD patients with pituitary adenomas. The primary hAD-MSCs were obtained from the abdominal subcutaneous adipose tissues of two non-PD patients, which were a 48-year-old female and a 28-year-old male with pituitary adenomas, from the subclavicular subcutaneous adipose tissues of two idiopathic PD patients, which were a 65-year-old female and a 68-year-old male, and from the subclavicular subcutaneous adipose tissues of two Parkin-defect PD patients which were a 26-year-old female and a 36-year-old female. The primary hAD-MSCs of the PD and non-PD patients were isolated from adipose tissues as previously described  and maintained in Mesenchymal Stem cell Expansion medium (Millipore, Billerica, MA, USA). The culture medium was replaced every 3 days. Phenotypical characterization and quantitative analyses of the putative hAD-MSCs were previously described . Simultaneously, the brain cortex tissues of early onset and idiopathic PD patients were obtained from DBS surgery (IRB No. H-0812-046-266) and immediately frozen and stored at -80℃ in a deep freezer while that of non-PD resected from patients was from normal brain tissue banking (IRB No. H-0805-036-243).
The day before transfection, cells were replated in a 24-well plate without antibiotics so that they would reach 90% confluence on the day of transfection. For each well, 50 µL of serum-free OPTI-MEM I Medium (Gibco BRL, Grand Island, NY, USA) containing 1 µg of pGRN145 plasmid (Geron Corporation, Menlo Park, USA) was combined with 50 µL of OPTI-MEM I Medium containing LIPOFECTAMINE LTX Reagent (Gibco BRL, Grand Island, NY, USA). The pGRN145 construct consisted of a mammalian expression vector containing the hTERT open reading frame minus the 5' and the 3' UTR under the control of the myeloproliferative sarcoma virus promoter (MPSV LTR). The mixture was then added to each well and the plate was gently shaken. After 24 h of incubation at 37℃, the culture medium was changed with fresh medium. After 48 h, the transfected cells were plated in medium containing Hygromycin-B in PBS (30 µg/mL, Invitrogen, Carlsbad, CA, USA) for two to three weeks. After treatment, cell death occurs rapidly allowing for the selection of transfected cells and single-cell derived clones were selected and expanded. After which, the concentration of Hygromycin-B was reduced to 10 µg/mL.
The telomerase activity was assayed with TRAP using the TRAPEZE® Telomerase Detection Kit (Chemicon International, Temecula, CA, USA). Cultured cells were solubilized in 200 µL of CHAPS lysis buffer (10 mM Tris-HCl pH 7.5, 1 mM MgCl2, 1 mM EGTA, 0.1 mM Benzamidine, 5 mM β-mercaptoethanol, 0.5% CHAPS, 10% Glycerol). Five hundred nanograms of protein from each sample buffer were used in the TRAP assay. The assay mixture in TRAP buffer (20 mM Tris-HCl pH 8.3, 1.5 mM MgCl2, 63 mM KCl, 0.05% Tween-20, 1 mM EGTA) contained the following: 50 µM dNTPs, 2 µg/mL TS primer, primer mix and 5 U/µL Tag polymerase (Promega). To test the specificity of the telomerase assay, 2 µL of cell extracts were pre-incubated at 85℃ for 10 min and then added to heat inactivated control mixtures. Two microliters containing 500 cells of TSR8 (control template) were used as a positive control for telomerase activity. As negative controls, 2 µL of primary
To establish whether the immortalized lines were euploidy, the cells were subjected to metaphase mitotic arrest using Colcemid (Gibco) stock solution. After which, the cells were harvested by centrifugation at 1,500 rpm, subjected to hypotonic shock with 0.075 M KCl, and fixed by adding Carnoy's fixative (3:1 methanol:acetic acid) and Giemsa staining (GTG banding). Prepared cell slides were then analyzed with the Karyotype Analysis program ChIPS-Karyo (Chromosome Image Processing System) (GenDix, Inc. Seoul, Korea).
The activity was determined in isolated mitochondrial preparations. We measured complex I activity as described in  with some modifications. We measured complex I spectrophotometrically at 600 nm in an incubation volume of 240 µL containing 25 mM potassium phosphate, 3.5 g/L BSA, 60 µM DCIP, 70 µM decylubiquinone, 1.0 µM antimycine-A and 3.2 mM NADH, pH 7.8. The obtained mitochondrial samples (1 µg/10 µL) were added to buffer without NADH. We preincubated the samples in the mixture for 3 min at 37℃. After adding 5 µL of 160 mM NADH, the absorbance was measured at 30-s intervals for 5 min at 37℃. After 5 min, we added 2.5 µL of rotenone (1 mM in dimethylsulfoxide and diluted to 100 µM in 10 mM Tris, pH 7.6) and measured the absorbance at 30-s intervals for 5 min at 37℃.
The activity was determined in isolated mitochondrial preparations. We measured the complex II activity as described in  with some modifications. We measured the complex II activity spectrophotometrically at 600 nm in an incubation volume of 240 µL containing 80 mM potassium phosphate, 1 g/L BSA, 2 mM EDTA, 0.2 mM ATP, 10 mM succinate, 0.3 mM potassium cyanide, 60 µM DCIP, 50 µM decylubiquinone, 1 µM antimycine-A and 3 µM rotenone, pH 7.8. Specifically, the obtained mitochondrial samples (1 µg/10 µL) were added to buffer without succinate and potassium cyanide. We preincubated the samples in the mixture for 10 min at 37℃. After adding 20 µL of 1.5 M succinate and 0.75 µL of 0.1 M KCN, the absorbance was measured at 30-s intervals for 5 min at 37℃. Blanks were measured in the presence of 5 mM malonate that was added before preincubation.
The activity was determined in isolated mitochondrial preparations. We measured the complex IV activity as described in  with some modifications. We measured the complex IV activity spectrophotometrically at 550 nm in an incubation volume of 240 µL containing 30 mM potassium phosphate, 2.5 mM dodecylmaltoside and 34 µM ferrocytochrome c, pH 7.4. Specifically, the obtained mitochondrial samples (1 µg/10 µL) were added to the buffer and their absorbance was immediately measured at 30-s intervals for 5 min at 30℃. Blanks were measured in the presence of 1 mM KCN.
The activity was determined in isolated mitochondrial preparations. We measured the citrate synthase activity as described in  with some modifications. We measured the citrate synthase activity spectrophotometrically at 412 nm in an incubation volume of 240 µL containing 50 mM Tris-HCl, 0.2 mM 5,5'-dithiobis-(2-nitrobenzoic acid), 0.1 mM acetyl-CoA and 0.5 mM oxaloacetate, pH 7.5. Specifically, the obtained mitochondrial samples (1 µg/10 µL) were added to the buffer without oxaloacetate. We preincubated the samples in the mixture for 5 min at 30℃. After adding 2.5 µL of 50 mM oxaloacetate, the absorbance was measured at 30-s intervals for 5 min at 37℃. The assay was initiated by the addition of oxaloacetate, and an equivalent volume of water was added to the controls.
Cells were washed in cold PBS and lysed in lysis buffer (cell signaling) and PMSF at 4℃. The lysates were clarified by centrifugation to remove the insoluble components at 15,000 g for 20 min at 4℃. The protein content of the cell lysates were normalized with Bradford reagent (Bio-Rad). Equal amounts of proteins, which were the same amounts used for the immortalized cells, were loaded onto a SDS-PAGE gel, electrophoresed, transferred to a PVDF membrane (Millipore) and blocked with 5% non-fat dry milk in TBST. The immunoreactive proteins on the membrane were detected with chemiluminescence using the ECL-Plus substrate (GE Healthcare, Buckinghamshire, USA) on X-ray films. Antibodies for HSP60, HSP90, Cytochrome b5 and GRP78 were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Prohibitin and β-actin (Santa Cruz) were used as internal controls. Western blot analysis was performed with the National Institutes of Health image processing and analyzing program (ImageJ, v1.38; http://rsb.info.nih.gov/ij/).
Cells grown on culture dishes were washed in PBS and fixed with 0.1% glutaraldehyde and 4% paraformaldehyde in PBS at 4℃ for 2 h. The cells were collected and centrifuged at 2,000 g for 3 min at 4℃ to obtain pellets. The prepared pellets were re-suspended in warm agar (1% in PBS) and centrifuged at 2,000 g for 3 min at 4℃ to obtain the pellets again. Then, the pellets were washed with PBS three times, and the cell pellets embedded with agar were fixed again with 1% osmium tetroxide for 2 h and washed with PBS three times. The cell pellets embedded with agar were dehydrated with an ethanol series and fixed again with Epon 812. The ultrathin (70 nm) sections were collected on Formvar/carbon-coated nickel grids, and the grids were stained with 2.5% uranyl acetate for 7 min followed by lead citrate for 2.5 min, and then, the sections were observed with a JEOL JEM-1011 electron microscope.
hAD-MSCs (1.5 × 104 cells) were seeded on gelatin-coated glass coverslips (NUNC, Rochester, USA). The next day, Mitotracker (Invitrogen, final 10 nM) in medium was added to the cells for 20 min at RT. The cells were washed with media and PBS and fixed with 4% PFA for 10 min at RT. After washing with PBS three times, the fluorescence was visualized with a confocal laser scanning microscope (Carl Zeiss LSM 510META, Carl Zeiss, Jena, Germany).
The cells were fixed with 4% paraformaldehyde in PBS. After permeabilization with 0.3% Triton X-100 in PBS and blocking with 10% normal goat serum (NGS) in 0.1% BSA/PBS for 1 h, immunofluorescent staining was performed using the primary antibody anti-mitochondria (Millipore Corporation, Billerica, MA, USA). Subsequently, the cover glasses were incubated for 1 h at RT with a fluorescent-labeled secondary antibody anti-FITC (Alexa488-labeled, raised in mouse; Jackson ImmunoResearch Laboratories, West Grove, PA, USA) and mounted with Vectashield medium containing 4',6-diamidino-2-phenylindole (DAPI; Vector Laboratories Inc., Burlingame, CA, USA). The fluorescence was visualized using a confocal laser scanning microscope (Carl Zeiss LSM 510META, Carl Zeiss, Jena, Germany).
Human brain tissues in a nitrogen tank were thawed and placed for seven days in a 50 ml conical tube containing ice-cold 4% paraformaldehyde. The human brain tissues were then cut into 15-µm thick sections on a freezing cryostat (Leica CM3000, Leica, Solms, Germany). The brain sections were washed in distilled water followed by washing with PBS three times for five minutes each and permeabilized with PBS containing 0.05% (vol/vol) saponin and 5% (vol/vol) NGS for 15 min. Non-specific binding was blocked with 1.5% NGS for 15 min. This was followed by application of the mouse monoclonal anti-mitochondria antibody (Millipore Corporation, Billerica, MA, USA) incubated overnight at 4℃. After being washed three times in PBS for five minutes each, the sections were incubated with the fluorescent-labeled secondary antibodies Alexa 594 goat anti-mouse or rabbit IgG (1:500) for 1 h at RT followed by washing with PBS. The fluorescently labeled slices were analyzed on a Meta confocal microscope (LSM 510; Carl Zeiss MicroImaging, Inc., Jena, Germany) equipped with four lasers.
Statistical analysis was performed with GraphPad Prism v. 5.0 (GraphPad Software, San Diego, CA, USA). Summary data are expressed as the means±standard deviation (SEM). The significance of the differences between the means was determined with unpaired Student's t-tests and ANOVA. A difference with a p-value<0.05 was considered significant while a p-value<0.001 was considered highly significant.
To assess the utility of hTERT overexpression as a means of immortalizing adipose tissue-derived mesenchymal stromal cells, subcutaneous adipose tissues were obtained from PD patients treated with DBS surgery. The hAD-MSCs were isolated from human adult patients with early-onset hereditary familial Parkin-defect PD as well as late-onset idiopathic PD for comparison with non-PD patients with pituitary adenomas. The hAD-MSCs from patients with idiopathic PD were designated as "
There was significant induction of strong telomerase activity during the immortalization of the hAD-MSCs. Fig. 1B shows the chromosomal structures of the cells obtained immediately after the immortalization and after culturing the immortalized
Mitochondrial structural defects are considered as one of underlying mechanisms associated with PD, the morphologies of the mitochondria were examined in the primary and immortalized
Mitochondrial dysfunction is mainly characterized by the generation of reactive oxygen species (ROS), a decrease in mitochondrial complex I enzyme activity, cytochrome-c release, ATP depletion and caspase 3 activation . The Parkin protein is consists of 465 amino acids with a molecular weight of 52 kDa and functions as a RING-type ubiquitin protein ligase, which possibly impairs the activity of the ubiquitin-proteosomal system and antioxidant defenses and enhances OS. Systemic mitochondrial complex I deficiency has long been implicated in the pathogenesis of idiopathic PD, which may generate additional OS in nigral neurons . Here, the activity of the mitochondrial respiratory enzymes was investigated in patients with idiopathic and Parkin deficiency (Fig. 3). Both of the immortalized idiopathic and Parkin-defect cells exhibited significant reductions in the mitochondrial complex I activity by 52.7% (p<0.0001) and 34.9% (p<0.001), in complex II by 44.2% (p<0.0001) and 39.9% (p<0.0001), and in complex IV by 51.8% (p<0.0001) and 39.0% (p<0.001), respectively, compared to the wild type cells (Fig. 3A). The immortalized idiopathic cells had greater reductions in the mitochondrial complex I, II, and IV activities than that of the Parkin-defect cells. The expression level of proteins for the mitochondrial preparations of the immortalized cells were normalized with the mitochondrial marker prohibitin, not with the cytosolic marker actin (Fig. 3B).
After investigating the key roles of mitochondrial dysfunction in PD pathogenesis in the established wild type, idiopathic and Parkin-defect mesenchymal stromal cells isolated from the adipose tissues of PD patients, comparative Western blot analyses were first performed to identify the expression of specific marker proteins (Fig. 4). There was a slight increase in a mitochondrial chaperone heat shock protein 60 (HSP60) in the immortalized cells (Fig. 4A). In addition, the altered expression of a molecular chaperone heat shock protein 90 (HSP90) was observed in the immortalized cells (Fig. 4B). Moreover, cytochrome b5, a ubiquitous electron transport hemoprotein, and GRP78, a central regulator of endoplasmic reticulum homeostasis, showed a slight increase in the mitochondrial fraction of the idiopathic and Parkin-defect immortalized cells (Fig. 4C). The expression level of proteins for the mitochondrial preparations of the immortalized cells were normalized with the mitochondrial marker prohibitin, not with the cytosolic marker actin (Fig. 4C).
Defective mitochondrial function and increased OS are known to have key roles in the pathogenesis of PD, which contribute to the selective loss of dopaminergic neurons in PD. Mitochondrial abnormalities have mainly been reported in various non-dopaminergic cells and tissue samples from human patients as well as transgenic mouse and fruit fly models of PD [4, 6]. Thus, mitochondria represent a promising target for the development of PD biomarkers. Biochemical detection methods for potential biomarkers of PD include genetic screening, mitochondrial complex I measurements, and α-synuclein levels and its isoforms in the blood [2, 3]. However, the limited availability of dopaminergic cell lines has prevented investigation of mitochondrial abnormalities in PD. For the first time, we have established hTERT-immortalized wild type, idiopathic and Parkin-defect MSCs isolated from the adipose tissues of PD patients. In order to overcome the cellular senescence of primary cultured hAD-MSCs of PD patients, the wild type, idiopathic and Parkin-defect MSCs were isolated from the adipose tissues of PD patients which were immortalized by hTERT. These hTERT-immortalized hAD-MSC cell lines established from patients with idiopathic and familial Parkin-defect PD had different activities in mitochondria function and in the morphologies of their structures, which could help in understanding better the pathogenesis of PD. Finally, these hTERT-immortalized hAD-MSC cell lines described in this study had altered PD specific markers, which could contribute to the development of early diagnostic markers and effective therapy targets for PD. One possible concern is that we used the control patients with pituitary adenomas. However, we may not consider that the adipose tissue taken from the abdominal sites of patients with pituitary adenomas had the characteristics of a tumor linked to mitochondrial changes. We usually collected normal adipose tissues from the patients to reconstruct the sellar floor after transsphenoidal adenomectomy. Therefore, we might suppose that the abdominal adipose tissue-derived mesenchymal cells of two patients with pituitary adenomas were normal cells.
Exogenous hTERT expression has been shown to extend both safely and effectively cellular lifespan and remove senescence as a major obstacle in tissue engineering and cell based therapies . Unexpectedly, we produced transformed immortalized cell lines with a chromosome abnormality. The karyotypes of these immortal cell lines were determined as aneuploidy with abnormal numbers of chromosomes ranging between 62~68. An extra or missing chromosome is a common cause of genetic disorders. Some cancer cells generally have abnormal numbers of chromosomes. According to the chromosomal numbers after culturing the six immortalized cell lines for one and two years, the structural phenotypes were similar with the only in difference being in the chromosomal numbers such as 3n=69. Therefore, we suggest that these one- and two-year cultures are the same immortalized cell lines with both cell lines having their variation in chromosomal numbers confirmed. Okubo et al. showed in detail that a change in the karyotypes of human B-lymphoblastoid cell lines transformed by Epstein-Barr virus during the process of immortalization was correlated to the development of telomerase activity using eight immortalized cell lines . It remains to be elucidated whether the chromosomal rearrangement is the cause of the immortalization accompanied by the strong telomerase activity or is a result of the immortalization process . Moreover, Belgiovine et al.  reviewed telomerase immortalization of somatic cells and its consequences and examined the complex role of telomerase in tumorigenesis. Cell lines with neoplastic transformation of telomerase expression can be useful models for studying molecular changes in human carcinogenesis.
There could be a possible correlation between chromosomal instability and the hTERT activity of the cell lines in this study. In the literature, there have been several reports on chromosomal instability driven by the hTERT activity. Fauth et al.  immortalized a panel of normal mammary fibroblasts and endothelial cells with the catalytic subunit of telomerase (hTERT) and a temperature-sensitive mutant of the SV40 large-tumor (tsLT) oncoprotein in different orders in early- and late-passage stocks. They maintained the immortalized cell lines in continuous culture for up to 90 passages, equivalent to >300 population doublings (PDs) post-explantation during 3 years of continuous propagation. They karyotyped the cultures at different passages. The cultures that received hTERT first followed by tsLT maintained a near-diploid karyotype for more than 150 PDs. However, in late-passage stocks (>200 PDs), the metaphase cells were mostly aneuploid. In contrast, the reverse order of gene transduction resulted in a marked early aneuploidy and chromosomal instability, already visible after 50 PDs. Tsuruga et al.  established two immortalized hepatocyte lines called HHE6E7T-1 and HHE6E7T-2 from human adult hepatocytes by introducing HPV16 E6/E7 and hTERT. Karyotype analysis showed that the HHE6E7T-1 cells remained near diploid but the HHE6E7T-2 cells showed severe aneuploidy at 150 PDs. Wen et al.  reported on the telomere-driven karyotypic complexity with p16INK4a inactivation in TP53-competent immortalized bone marrow endothelial cells by hTERT transduction. They showed a specific association between the p16INK4 inactivation and the evolution of karyotypic complexity in the TP53-competent cells. These results show that complex karyotypes can evolve in TP53-competent cells and provide evidence that p16INK4a functions as a gatekeeper to prevent telomere-driven cytogenetic evolution.
Although these immortalized cells had chromosomal aberrations, the telomerase activity was identified in six immortal cell lines over two years and in different passages in the extracts of human cells; however, three pre-immortal cell lines showed no telomerase activity and had normal diploid karyotypes. These methods were used to measure the telomerase activity in dividing cultures of various immortal cell lines and normal somatic cells derived from human adipose tissues. These results suggest that the telomerase activity is involved in telomerase maintenance, linking this enzyme to cell immortality. In this study, hAD-MSCs had mostly normal diploid karyotypes before immortalization; however, all had abnormal karyotypes after immortalization accompanied by strong telomerase activity. The pre- and post-immortalization of hAD-MSCs will be an effective system to study the mechanisms of not only the immortalization of hAD-MSCs, but also PD. These immortalized hAD-MSC cell lines established from patients with idiopathic and familial Parkin-defect PD while artificial could be used as a good cellular model to evaluate mitochondrial dysfunction in the pathogenesis of PD.
Previously, we investigated selective gene expression profiles derived from primary cultured AD-MSCs from PD patients with Parkin-defect PD as well as idiopathic PD using transcriptome cDNA microarray analysis . Our data was only preliminary; however, high throughput microarray screening using these cell lines has identified functional groups of genes affected by mitochondria dysfunction and OS. We analyzed PD-related differentially regulated genes by OS in
Heat shock proteins (HSPs or molecular chaperones) can either aid in the folding and maintenance of newly translated proteins or lead to the degradation of misfolded and destabilized proteins . HSPs are particularly important in PD because aberrant protein aggregation and neuron degeneration are common pathophysiologies of PD. HSPs have two main cellular functions. One is to promote the function of the ubiquitin-proteasome system (UPS) and the other is to inhibit apoptotic activity in PD . HSP60 is a mitochondrial chaperone that is constitutively expressed in the mitochondrial matrix. It functions to catalyze the proper folding and assemble of proteins imported into the mitochondria and to correct mis-folded proteins that have been damaged by OS . HSP90 has been recently identified as the predominant chaperone implicated in α-synuclein (AS)-evoked pathologies . Uryu et al.  showed that HSP90 together with ubiquitin massively co-localizes
Cytochrome b5 functions as an electron transfer component in a number of oxidation reactions . Increased cytochrome b5 levels in idiopathic and Parkin-defect cells may be because of compensatory mechanisms in response to the defective electron flows from ETC enzyme dysfunction. Specifically, increased cytochrome b5 may help to facilitate electron transfer from NADH to cytochrome c . The ER stress response, also termed the unfolded protein response (UPR), serves to protect cells against the toxic build-up of un-/mis-folded proteins. The first step in UPR is the recognition of unfolded proteins by the HSP70-class chaperone glucose regulated protein 78, also known as BiP (GRP78/BiP). Recently, Gorbatyuk et al. suggested that the molecular chaperone GRP78/BiP plays a neuroprotective role in α-synuclein-induced Parkinson-like neurodegeneration . Our data showed increased levels of GRP78 in the idiopathic and Parkin-deficient cells, which possibly could also explain the compensatory mechanisms.
In conclusion, for the first time, we have established hTERT-immortalized wild type, idiopathic and Parkin-defect mesenchymal stromal cells isolated from the adipose tissues of patients. We have showed that the hTERT-immortalized hAD-MSC cell lines established from patients with idiopathic and familial Parkin-defect PD could be used as good cellular models to evaluate mitochondrial dysfunction to understand better the pathogenesis of PD and to develop early diagnostic markers and effective therapy targets for PD. Noticeably, PD-specific mitochondrial dysfunction included reduced complex I, II, and IV enzyme activities, abolished cristae and accumulated mitochondria that were damaged. The OS-induced pathological signaling involves the altered expressions of PD specific markers. Further functional characterization of mitochondria DNA and whole genome sequencing analysis may help to explain the complex pathogenesis of PD in dopamine neurons and in the development of novel therapeutic agents for PD.