Real-time monitoring of circadian clock oscillations in primary cultures of mammalian cells using Tol2 transposon-mediated gene transfer strategy
- Kazuhiro Yagita†1, 2, 5Email author,
- Iori Yamanaka†2, 5, 6,
- Noriaki Emoto3, 5,
- Koichi Kawakami4, 5 and
- Shoichi Shimada1, 5
© Yagita et al; licensee BioMed Central Ltd. 2010
Received: 22 May 2009
Accepted: 22 January 2010
Published: 22 January 2010
The circadian rhythm in mammals is orchestrated by a central pacemaker in the brain, but most peripheral tissues contain their own intrinsic circadian oscillators. The circadian rhythm is a fundamental biological system in mammals involved in the regulation of various physiological functions such as behavior, cardiovascular functions and energy metabolism. Thus, it is important to understand the correlation between circadian oscillator and physiological functions in peripheral tissues. However, it is still difficult to investigate the molecular oscillator in primary culture cells.
In this study, we used a novel Tol2 transposon based Dbp promoter or Bmal1 promoter driven luciferase reporter vector system to detect and analyze the intrinsic molecular oscillator in primary culture cells (mouse embryonic fibroblasts, fetal bovine heart endothelial cells and rat astrocytes). The results showed circadian molecular oscillations in all examined primary culture cells. Moreover, the phase relationship between Dbp promoter driven and Bmal1 promoter driven molecular rhythms were almost anti-phase, which suggested that these reporters appropriately read-out the intrinsic cellular circadian clock.
Our results indicate that gene transfer strategy using the Tol2 transposon system of a useful and safe non-viral vector is a powerful tool for investigating circadian rhythms in peripheral tissues.
The circadian clock is driven by a stable and robust self-sustaining molecular oscillator. This oscillation machinery resides in most of the cells in our body, and even cultured cell lines also have an intrinsic circadian oscillator [1–3]. The molecular oscillation of circadian clock consists of interlocked positive and negative transcription/translation feedback loops (TTFL) involving a set of clock genes, and clock-controlled output genes that link the oscillator to clock-controlled processes . CLOCK and BMAL1 are basic-helix-loop-helix (bHLH) PAS transcription factors that heterodimerize and transactivate the core clock components such as Period (Per1,2,3), Cryptochrome (Cry1 and Cry2) and Rev-Erbα [4–6]. Then, PER and CRY proteins suppress the activity of the CLOCK/BMAL1, whereas REV-ERB α suppresses Bmal1 gene expression.
Promoters of clock genes that show cyclic transcription often contain circadian enhancers such as E-box and RRE (Ror responsive element), and these circadian enhancer-containing promoters can drive cyclic expression of luciferase gene as a reporter . Using the bioluminescence reporters, we recently established real-time circadian clock analysis system in living cells .
It is important to investigate the correlation between circadian oscillator and physiological functions in each differentiated cell. However, it is difficult to investigate the molecular oscillator of primary culture cells because of the difficulty to read-out the intrinsic circadian rhythm. In this study, we describe the successful detection and analysis of the intrinsic molecular oscillator in primary culture cells such as mouse embryonic fibroblasts (MEF), fetal bovine heart endothelial cells (FBHE) and rat astrocytes using Tol2 transposon-based vector system. The Tol2 transposon system is a useful method to generate stably transfected luciferase-expressing cells even in primary culture cells. We were able to monitor circadian clock oscillations by real-time monitor system. We propose that the Tol2 transposon-based vector system is a simple and safe non-viral technique that can be used for various types of cells.
Efficiency of Tol2 transposon-based gene transfer
Since these results suggested that Tol2 transposon-based vector system markedly improved transgenic efficiency in cultured mammalian cell line, we next examined whether Tol2 transposon was effective also in stable transfection into primary cultures of MEF, rat astrocytes and FBHE cells. Among these, rat astrocytes were difficult to evaluate the efficiency of stable transfection, because they did not form colonies and the viability rate after transfection was too low for meaningful quantitative analysis. In this assay, Bmal1:luc-pT2A plasmid was used to exclude possible plasmid-specific events. Quantitative analysis showed extremely high efficient stable transfection rates in not only rat-1 cell line but also both MEF and FBHE cells (Fig. 2C). In addition to Dbp:luc-pT2A vector, the Bmal1:luc-pT2A vector also allowed the generation of stably transfected rat-1 cell line with over 18-fold higher efficiency, under Tol2 transposase expression. Strikingly, the expression of transposase allowed the generation of both MEF and FBHE cells stably transfected with Bmal1:luc-pT2A with extremely higher efficiency (24-fold and 21-fold, respectively) (Fig. 2C). These results also indicate that our Tol2 transposon system is an useful tool for gene transfer into mammalian primary culture cells.
Real-time monitor of circadian clock oscillation in Dbp:luc or Bmal1:luc stably transfected primary culture cells
In this study, first we showed that the Tol2 transposon system is a useful technique in generating stable transfected primary culture cells and, second, we demonstrated that the Tol2 transposon system is applicable to the study of circadian clock oscillations.
The Tol2 transposon was originally discovered from Medaka fish (Orzyias latipes) . An active autonomous member of Tol2 was first identified by the analysis using zebrafish embryos . Since then, the Tol2 transposon system has been mainly used for random insertion mutagenesis and transgene in zebrafish . Although recent reports have indicated that the transposon systems such as piggyBac and SleepingBeauty in addition to Tol2 are also active in mammalian cells [15, 16], few studies have been reported that utilized the Tol2 system for transfection to mammalian primary culture cells. In the present study, we showed that the Tol2 transposon system is a useful tool in generating stable transfected primary culture cells such as MEF and fetal bovine heart endothelial cells.
As previously reported, transfection of primary cells have been also performed by using retroviral vectors . Comparing with the retroviral vectors, the number of the stably transfected cells obtained after selection culture is small in Tol2 transposon system. However, the handling is easier because Tol2 transposon system requires only co-transfection of two plasmids. Furthermore, it is much safer than retroviral vectors. These features should be enough reason to choose the Tol2 transposon system for many researchers instead of retroviral vector system.
We demonstrated that the Tol2 transposon system is applicable to the study of circadian clock oscillation. In this study, we were able to detect circadian clock oscillations in primary culture cells including MEF, astrocytes and FBHE cells expressing Bmal1 promoter- or Dbp promoter-driven luciferase. All generated cells exhibited robust daily cycles of bioluminescence, and there was no obvious difference of observed features between Tol2-system and usual DNA transfection methods experienced before [8, 18].
In obtained stably transfected cells using Tol2 system, the oscillation phase was almost identical; even different types of cells such as FBHE cells and astrocytes were stably integrated with Bmal1:luc reporter by the Tol2 system (Fig. 3A-D). Moreover, as seen in endogenous gene expression patterns, these cells showed almost opposite phases of Bmal1:luc driven rhythms and Dbp:luc driven rhythms (Fig. 3E). These phase-relationship of circadian oscillation indicate that the integrated reporter correctly read-out the intrinsic circadian clock system.
In addition, our results are the first to demonstrate circadian clock oscillations in primary endothelial cells in real-time manner. Previous studies suggested the importance of circadian regulation of endothelial function for various kinds of physiological and pathological events such as blood pressure and endothelial proliferation . However, little is known about the molecular relationship between circadian clock and endothelial function, because it has been difficult to analyze the circadian oscillation of primary endothelial cells.
Viral vector system is also very high-efficient gene transfer tools. Getting together, Tol2 transposon based vector system is useful and safe tool to investigate the circadian clock in various types of primary culture cells.
The Tol2 transposon-based assay system described in this study should enhance the biological analysis of molecular oscillator of circadian clock and the function of primary culture cells such as MEFs, rat astrocytes and fetal bovine heart endothelial cells. We were able to monitor the circadian clock oscillations by real-time monitor system in these cells. We propose that the Tol2 transposon-based vector system is a simple and safe non-viral technique that can be used for various types of cells.
For Bmal1:luc-pT2A vector, 0.5 kb of the 5' flank region of mouse Bmal1 gene was cloned by PCR into pCR2.1-Topo vector. The Bmal1 promoter fragment was digested with BglII and HindIII, then subcloned into BglII/HindIII site of pGL4.15 vector . The BglII/SalI digested fragment of Bmal1-pro-pGL4.15, containing Bmal1 promoter, Luciferase and hygromycin-resistant gene, was subcloned into the BglII/XhoI site of the pT2AL200R150G vector.
For Dbp:luc-pT2A vector, the mDbp promoter:luciferase reporter construct (Dbp:luc-pGL4.11) was generated as reported previously . The Dbp promoter, luciferase fragment and hygromycin-resistant gene fragment obtained from Dbp:luc-pT2A and pTRE2-Hyg vectors were subcloned into the XhoI/BglII digested pT2AL200R150G Tol2 vector.
Cell culture and transfection
Rat-1 and mouse embryonic fibroblasts (MEF) were cultured in Dulbecco's modified Eagle medium (DMEM) with 10% fetal bovine serum (FBS). FBHE cells were cultured in DMEM with 10% FBS and 2 ng/ml of basic fibroblast growth factor (bFGF). Rat astrocytes were obtained from Human Science Research Resources Bank (HSRRB, Osaka, Japan), and cultured in DMEM with 10% FBS.
For transfection, 1 μg of Dbp:luc-pT2A or Bmal1:luc-pT2A and 1 μg of pCAGGS-TP or pcDNA3 plasmids were transfected using Fugene 6 reagent into 3 × 105 cells cultured in a 6-well plate. After overnight culture, the cells were trypsinized and plated in 9-cm dishes with culture medium for each type of cells as indicated above. In rat-1 cells, 1/100 of transfected cells were plated in 9-cm dishes. Selection with 250 μg/ml hygromycin-containing medium was started 24 hours after plating on the 9-cm dishes. After two or three weeks, surviving cell colonies were picked up using cloning rings. For rat astrocytes, cells did not form the colonies, thus surviving cells were gathered and cultured in 6- cm dishes after selection.
Real-time monitoring of cellular circadian oscillation
For real-time monitoring of cellular circadian oscillation, 1 × 105 hygromycin-resistant cells (rat-1, MEF, astrocytes and FBHE cells) were seeded in 24-well plates and cultured overnight with growth medium of each type of cells. Next, the medium was changed with a medium containing DMEM/F12, 10% FBS, 15 mM 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid (HEPES), 0.2 mM luciferin and 100 nM dexamethasone to synchronize the cellular circadian clocks. Bioluminescence was monitored using a photomultiplier-tube-based bioluminescence monitoring system . The bioluminescence was measured for 60 sec in every 20 minutes.
Phase analysis of cellular circadian oscillation
Phase analysis of cellular circadian rhythms are analyzed as previously reported [2, 20]. Briefly, second peaks after ssynchronization of bioluminescence of Dbp:luc-pT2A stably transfected MEF lines (n = 9) and second peaks of Bmal1:luc-pT2A stably transfected FBHE lines (n = 13) are determined using detrended and smoothed PMT based bioluminescence data.
We wish to thank Dr. T. Kondo (Nagoya University) for support and technical advice and discussion. We also thank Dr. Wataru Nakamura (Osaka University) for assistance of data analysis. This study was supported by a Grant-in-Aid (20590190, K.Y.) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
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