"Color Timer" mice: visualization of neuronal differentiation with fluorescent proteins
© Kanki et al; licensee BioMed Central Ltd. 2010
Received: 6 January 2010
Accepted: 2 February 2010
Published: 2 February 2010
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© Kanki et al; licensee BioMed Central Ltd. 2010
Received: 6 January 2010
Accepted: 2 February 2010
Published: 2 February 2010
The molecular mechanisms governing the differentiation of neural stem cells (NSCs) into neuronal progenitor cells and finally into neurons are gradually being revealed. The lack of convenient means for real-time determination of the stages of differentiation of individual neural cells, however, has been hindering progress in elucidating the mechanisms. In order to be able to easily identify the stages of differentiation of neural cells, we have been attempting to establish a mouse system that would allow progression of neuronal differentiation to be visualized based on transitions between fluorescence colors by using a combination of mouse genetics and the ever-expanding repertoire of fluorescent proteins. In this study we report the initial version of such a mouse system, which we call "Color Timer." We first generated transgenic (Tg; nestin/KOr Tg) mice in which production of the fluorescent protein Kusabira-Orange (KOr) is controlled by the gene regulatory elements within the 2nd intronic enhancer of the nestin gene, which is a good marker for NSCs, so that NSCs would emit orange fluorescence upon excitation. We then confirmed by immunohistochemical and immunocytochemical analyses that the KOr fluorescence closely reflected the presence of the Nestin protein. We also confirmed by a neurosphere formation assay that the intensity of the KOr fluorescence correlated with "stemness" of the cell and it was possible to readily identify NSCs in the two neurogenic regions, namely the dentate gyrus of the hippocampus and the subventricular zone of the lateral ventricle, in the brain of adult nestin/KOr Tg mice by the orange fluorescence they emitted. We then crossed nestin/KOr mice with doublecortin-enhanced Green Fluorescent Protein Tg mice, whose immature neurons emit green fluorescence upon excitation, and it was possible to visualize the progress of NSC-to-neuron differentiation by the transition between fluorescence colors from orange to green. This two-color initial version of the "Color Timer" mouse system will provide a powerful new tool for neurogenesis research.
Identification and purification of the Green Fluorescent Protein (GFP) and cloning of its gene revolutionized the biological sciences, because labeling specific cell types, protein tracing, and real-time monitoring of gene expression in living cells, among other things, became possible for the first time [1, 2]. A number of other fluorescent proteins (FPs) that possess distinct characteristics have been discovered and/or engineered since then and the ever-expanding repertoire of FPs has made it possible to label individual cells with different color of fluorescence reporters in the same animal, as, e.g., in "Brainbow" mice [3, 4].
The long-term goal of our research is to establish a mouse system in which it will be possible to visualize neuronal differentiation from neural stem cells (NSCs) to neuronal progenitor cells (NPCs) and then to neurons based on transitions between the colors of the fluorescence. To achieve that goal we decided to use a combination of mouse genetics and FPs to regulate the production of different color FPs by different gene regulatory elements (GREs), each of which is specific to a different cell type, in the mouse brain.
As a first step, we attempted to establish a two-color first version of such a mouse system, which we called "Color Timer." We began by generating transgenic (Tg) mice whose NSCs, upon excitation, emit fluorescence of a color that is readily distinguishable from green, which has already been used in hundreds of reporter mouse lines. One of the most-widely-used markers for NSCs is the ~200-kDa intermediate filament protein Nestin . Thorough investigation of the regulation of the nestin gene has revealed the importance of the second intronic enhancer as the main regulator of the NSC-specific expression of the gene . A number of reporter Tg mouse lines have already been generated with this nestin second intronic enhancer, proving the usefulness of the element in driving expression of the gene in NSCs [7, 8]. We therefore decided to use it, in combination with the nestin promoter, as the driver of production of the FP in our Tg mice .
All the animal-related procedures employed in this study were conducted according to the institutional regulations.
The 10 founders were crossed with wild-type B6 animals to obtain F1 progeny and they were examined for the orange fluorescence of KOr. KOr fluorescence was detected in the brains of embryonic day-14.5 (E14.5) embryos of 4 (#s 20, 48, 55, and 70) of the 10 lines (Figure 1B). As can be seen in Figure 1B, the KOr signals in the cerebral cortex of line #55 showed a scattered distribution pattern that was totally different from the patterns in the other lines. Among the other three lines, the intensity of the KOr signals was highest in line #70, intermediate in line #48, and lowest in line #20. By 8 weeks after birth (P8w), the KOr signal intensity in line #48 had become similar to its intensity in line #70, whereas the signal intensity in line #20 remained weak (data not shown).
To investigate the correlation between the intensity of the orange fluorescence and the levels of expression of the nestin gene in individual KOr-positive cells, we performed an immunocytochemical analysis of cells prepared from the brains of E14.5 nestin/KOr Tg mouse embryos. Dissociated cells from line #70 animals were immunocytochemically processed with an anti-Nestin antibody, which was in turn recognized by an Alexa Fluor 488-conjugated secondary Ab. The processed cells were then analyzed for orange and green fluorescence with a cell sorter.
These results indicated that the intensity of the KOr fluorescence closely reflected the levels of expression of the endogenous nestin gene in nestin/KOr mouse line #70.
When cultured in a suspension containing growth factors such as epidermal growth factor (EGF) and basic fibroblast growth factor (bFGF), NSCs proliferate and form floating masses of cells called "neurospheres" and the number and size of the neurospheres have been used as a measure of "stemness" . This "neurosphere formation assay" is one of the systems most widely used to evaluate the stemness of neural cells and we used it to examine the relationship between the orange fluorescence and stemness of the KOr-positive cells as described in our previous reports [7, 8].
Cells were prepared from the brains of E14.5 line #70 nestin/KOr mice and after sorting them into several populations according to the intensity of the KOr fluorescence, we submitted them to a neurosphere formation assay. As shown in Figure 3B, there was a positive correlation between the intensity of the KOr fluorescence and stemness assessed by the frequency of neurosphere formation.
Based on all of these findings taken together, we concluded that NSCs can be prospectively enriched as orange fluorescent cells from nestin/KOr Tg mouse line #70, whose potency is positively correlated with the intensity of the orange fluorescence they emit.
The concept of "adult neurogenesis" is now well accepted and it is widely known that new neurons are constantly generated in two neurogenic regions in the adult mammalian brain: the dentate gyrus (DG) of the hippocampus and the subventricular zone (SVZ) of the lateral ventricle (LV). Since the orange signals of KOr should be observed in these regions as new neurons are generated from NSCs, we examined the distribution of KOr-positive cells in these two regions of adult (P8w) mice.
In the other neurogenic area, the SVZ, the KOr fluorescence signals were distributed along the wall of the LV (Figure 4B). This pattern closely overlapped the pattern of distribution of immunohistochemically-detected Nestin protein, especially at the dorsolateral corner (bottom panels).
Taken together, these findings confirmed the usefulness of nestin/KOr Tg mouse line #70 as an NSC reporter.
We then considered which mouse line to use to fluorescence label neurons. With our future plan to separate neurons into immature and mature subpopulations in mind, we searched for a good specific marker for immature neurons.
Among the several candidates we considered, we selected Doublecortin (DCX), a ~45-kDa microtubule-associated protein already being widely used as a marker for immature neurons. The usefulness of DCX as a marker of immature neurons has been clearly demonstrated by the immunohistochemical work of the Aigner laboratory .
In addition to several conventional Tg mouse lines, a Tg mouse line with a bacterial artificial chromosome (BAC) backbone containing the genomic region around the mouse DCX gene was generated by the GENSAT project, whose mission is to construct an array of EGFP reporter mice by using BAC backbones with genes expressed in the nervous system . This DCX-EGFP BAC Tg mouse line was used to confirm that the intensity of EGFP, which reflects the amount of the DCX protein within the cell, can be used as an indicator of neuronal maturation, which confirmed the usefulness of this mouse line as a reporter for neurons . By combining this mouse line with the nestin/KOr Tg that we had generated, we hoped to be able to establish a mouse system in which the NSC-to-immature neuron differentiation could be visualized as a transition from orange to green fluorescence.
Double Tg mice were obtained by crossing nestin/KOr and DCX-EGFP animals, both of which were heterozygous, according to the Mendelian ratio as expected.
To determine whether the expected transition from orange-to-green fluorescence actually occurred during the process of NSC-to-neuron differentiation in developing mouse brains, we performed time-lapse imaging of the embryonic cerebral cortex of double Tg mice.
As expected, most of the orange cells in the double Tg animals resided on the apical side of the cortex, and the green cells were located on the cortical side. Additional file 2 shows time-lapse images of the cerebral cortex of a double Tg mouse generated by using nestin/KOr line #70. Although it is rather difficult to identify individual orange cells on the apical side of the cortex because of the ubiquitous expression of the KOr transgene in the region, an orange-to-green fluorescence transition was occasionally observed in individual cells and a typical example is indicated by an arrow in Additional file 2.
The cortex of a double Tg mouse generated by using nestin/KOr line #55 is shown in Additional file 3. The scattered distribution of KOr-positive cells made identification of yellow cells much easier than in line #70.
Taken together, these results demonstrate that the color of the fluorescence that neural cells emit upon excitation actually does change from orange to green during neuronal differentiation.
As mentioned above, NSCs cultured in suspension in the presence of growth factors such as EGF and bFGF proliferate and form floating masses of cells called neurospheres. Since the cells undergo differentiation in parallel with self-renewal, practically all neurospheres consist of mixtures of different types of neural cells, including NSCs, neurons, and glia. To determine whether it would be possible to visualize the differentiation of NSCs into neurons in neurospheres as well, we also performed time-lapse imaging of neurospheres prepared from the cerebral cortices of E14.5 double Tg embryos with line #70 of nestin/KOr (Additional file 4).
In most of the spheres, the majority of the orange signals were found in the middle with green cells surrounding them, although the distribution of fluorescent colors was reversed (green inside and red outside) in some spheres. Yellow cells, which are presumably in the NSC-to-neuron transition phase were also observed.
KOr fluorescence was most intense along the wall of the LV, and as cells migrated and passed the dorsolateral corner, the KOr fluorescence gradually diminished and became diffuse.
The green fluorescence of EGFP, on the other hand, was relatively weak around the LV but suddenly became intense as the cells approached the dorsolateral corner, and it remained intense for some distance. Strong yellow signals, corresponding to cells in which both KOr and EGFP were present, were clustered at the dorsolateral corner.
These observations confirmed the expected orange-to-green fluorescence transition during neuronal differentiation in the adult mouse brain.
Based on all of these findings taken together, we concluded that the transition between fluorescent colors from orange to green reflects NSC-to-neuron differentiation in both the embryonic brain and the adult brain, thereby demonstrating the usefulness of these animals as an NSC-to-neuron reporter.
The pioneering work by Chalfie and colleagues clearly showed the great potential of GFP as a reporter for real-time identification of a specific cell type . During the 15 years since then, thanks to the efforts of several laboratories, the FP repertoire has been expanded to the point that it now not only spans the visible spectrum, but also extends beyond it. By combining different color FPs with a number of cell-type-specific gene regulatory elements that have been identified to date, we have been trying to establish mouse systems in which neural cells can "tell what they are" by the color of the fluorescence they emit.
Based on the findings described above, we concluded that this two-color initial version of the "Color Timer" mouse system, as well as the more-advanced multi-color versions that we are currently generating, will provide a powerful new tool for neurogenesis research.
We are grateful to Dr. Masahiro Yamaguchi (U. of Tokyo; Japan) for the nestin promoter-enhancer construct; to Molecular Biological Laboratories (MBL; Nagoya, Japan) for the KOr cDNA and the numerical data for the KOr spectra; to the GENSAT Project for the DCX-EGFP BAC Tg mice; and to the "Tamago Club" of the Research Resource Center of RIKEN BSI for microinjection of the nestin/KO transgene DNA fragment. We are indebted to Yoichi "Yotan" Imaizumi for his advice in regard to the immunohistochemical analyses, to Sadafumi Suzuki and Dr. Yumi Matsuzaki for their help with cell sorting, to Chikako Hara for her help with preparing Additional file 1, and to Satoshi Suyama, François Renault-Mihara, and Chikako Hara for their advice in regard to time-lapse imaging. We also thank other members of the Okano and Miyawaki laboratories, in particular the members of the Adult Neurogenesis Group ("Minashigos") of the former for discussions, advice, encouragement, and/or entertainment throughout this study. This work has been supported by grants from the Ministry of Education, Culture, Sports, Science and Technology (MEXT; to HO, to HK) and from RIKEN BSI (to AM).
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