Bone loss is a serious problem in spaceflight; however, the initial action of microgravity has not been identified. To examine this action, we performed live-imaging of animals during a space mission followed by transcriptome analysis using medaka transgenic lines expressing osteoblast and osteoclast-specific promoter-driven GFP and DsRed. In live-imaging for osteoblasts, the intensity of osterix- or osteocalcin-DsRed fluorescence in pharyngeal bones was significantly enhanced 1 day after launch; and this enhancement continued for 8 or 5 days. In osteoclasts, the signals of TRAP-GFP and MMP9-DsRed were highly increased at days 4 and 6 after launch in flight. HiSeq from pharyngeal bones of juvenile fish at day 2 after launch showed up-regulation of 2 osteoblast- and 3 osteoclast- related genes. Gene ontology analysis for the whole-body showed that transcription of genes in the category “nucleus” was significantly enhanced; particularly, transcription-regulators were more up-regulated at day 2 than at day 6. Lastly, we identified 5 genes, c-fos, jun-B-like, pai-1, ddit4 and tsc22d3, which were up-regulated commonly in the whole-body at days 2 and 6, and in the pharyngeal bone at day 2. Our results suggested that exposure to microgravity immediately induced dynamic alteration of gene expression levels in osteoblasts and osteoclasts.
In the animal body, various cellular stimuli such as heat shock1, oxidative2, and hypoxic3 stresses have been studied attentively. In spaceflight, when gravitational alteration occurs rapidly with the shift to microgravity, changes in fluid shift and blood pressure quickly take place in the human body4, leading to hemodynamic adaptation5 and alteration of vasoreactivity, accompanied by up-regulation of the NO/cGMP pathway, as was found in an in vitro study6. These responses to the extreme change in gravity continuously happen at the whole-body level; however, the molecular mechanisms of such responses to “microgravitational stress” remain unclear.
Bone loss in astronauts, which is one of severe health problems, is observed in a spaceflight lasting for a few months, which loss is reminiscent of that for senile osteoporosis on the ground. It is recognized that understanding the potential action of this microgravity environment toward bone loss should contribute to progress in the fields related to the effect of mechanical stress on bone, as well as to clinical application for osteoporosis. To investigate the mechanism of bone loss during spaceflight, it is important to study the initial response immediately after the initial exposure to microgravity, because this response represents the trigger for bone loss. As to symptoms that appear early in orbit, the loss of calcium starts at least 10 days after launch7,8; and the assessment of bone quality revealed a loss of bone in short-duration spaceflight for 20 days9. These reports suggest that osteoblasts and osteoclasts undergo changes immediately after launch. In fact, in vitro experiments conducted during a short-term parabolic flight showed changes in gene expression and cellular cytoskeleton in human chondrocytes10,11. However, the nature of the initial response in vivo to microgravity in bone tissues is unclear.
One way to answer this question is to perform animal experiments at the ISS (International Space Station). In a previous study, we found that in skeletogenesis of the vertebral body and pharyngeal bone in medaka, their osteoblasts and osteoclasts revealed properties similar to those of their mammalian counterparts12,13,14,15. In osteoblast differentiation, osterix is a typical marker of early osteoblasts; and osteocalcin, one of late osteoblasts16, whereas TRAP (tartrate-resistant acid phosphatase), cathepsin K, and MMP9 are markers of osteoclasts17. In medaka as in mammals these cells are differentiated from TRAP, cathepsin K, and MMP9-positive mononuclear cells into multinuclear osteoclasts13,14,15. Furthermore, the c-fms (the receptor of M-CSF)-deficient zebrafish shows a reduced number of osteoclasts, resulting in a bone modeling defect14, which finding indicates the essential function of M-CSF and c-fms in fish as well as in mammals18. Moreover, RANKL, the essential osteoclast differentiation factor expressed in osteoblasts, is common between mammals and medaka fish19. All evidence taken together indicates that the basic molecular mechanism underlying the differentiation of osteoclasts is common between mammals and fish and that the interaction of these cells with osteoblasts plays a crucial role in osteoclast differentiation in medaka as well. To identify osteoblasts and osteoclasts in-vivo, we previously developed a medaka osterix promoter-DsRed transgenic line for the visualization of osteoblasts20 and a medaka TRAP promoter-GFP transgenic line for that of osteoclasts14. Finally, we established a double transgenic line of osterix-DsRed and TRAP-GFP21 to examine the cooperation between osteoblasts and osteoclasts in the same animal. In the analysis of pharyngeal bones, by using this double transgenic line we showed the important role of osteoblasts for controlling osteoclasts to modify the attachment bone during tooth replacement in medaka pharyngeal teeth15. The row of attachment bones is resorbed at the anterior side where most developed functional teeth are located, and generated at the posterior side where teeth are newly erupting, which actions cause continuous tooth replacement. Osteoclasts and osteoblasts are located at attachment bones separately, with mature osteoclasts being localized at the resorbing side and osteoblasts gathered at the generating side.
When medaka fish at 6 weeks after hatching were launched to the ISS in 2012 and reared there for 2 months, activation of osteoclasts together with bone loss occurred in the flight fish21. In that study, to examine the alteration of gene expression early in orbit, we preserved specimens with RNAlater at days 2 and 6 after launch. Another way to study growing tissues under microgravity in space is to perform experiments using three-dimensional cultures22; however, such experiments have not yet been performed at the ISS. In our present study, to examine the early effects of microgravity on bone cells, we embedded transgenic medaka larvae in a gel for a live-imaging study in space in 2014, and observed signals by fluorescence microscopy at the ISS via remote operation from Tsukuba Space Center. For this experiment, we utilized 4 different double medaka transgenic lines and, in particular, investigated up-regulation of fluorescent signals of osteoblasts and osteoclasts in these double transgenic lines as an important way to study osteoblast-osteoclast interaction under microgravity.
In addition, we examined the pattern of gene expression in these transgenic fish by transcriptome analysis. HiSeq analysis of the pharyngeal bones showed the enhanced expression of osteoblast- and osteoclast-related genes. Furthermore, GO (gene ontology) analysis showed the up-regulation of AP-1-, GR- and TGF-β-related genes that coincided with osteoclast activation. Our results about live-imaging and transcriptome analysis may prompt the establishment of a new field in gravitational biology.
Enhancement of osteoblast signals under microgravity
To find alteration of signal intensity and area of osteoblasts and osteoclasts, we observed the fluorescent signals in living medaka for 8 days at the ISS as shown in Methods and Table 1. Twelve larvae at stage 39 were embedded in “medaka chambers” (Fig. 1a), in which live larvae in a gel were covered with a semipermeable membrane. Pharyngeal bones, around which many osteoblasts and osteoclasts were localized, were clearly observed from the ventral side (Supplementary Fig. S1). This ventral side was oriented toward the glass plate for observation via an objective lens (Fig. 1b). For capturing images by use of a 20x lens, we carried out observation in 3 steps, because the posture of the living larvae was constantly changing (Fig. 1c). The experimental schedule for live-imaging of the 4 double transgenic lines, osterix-DsRed/TRAP-GFP, osteocalcin-DsRed/TRAP-GFP, MMP9-DsRed/RANKL-GFP, and cox2-GFP/TRAP-DsRed during 8 days in flight and on the ground is shown in Supplementary Table S1. To perform the imaging analyses for both the flight and ground samples under the same conditions, we manipulated both fluorescence microscopes, one at ISS and the other on the ground at the same gain value and the same appropriate exposure time (Supplementary Table S2). Firstly, the capture images of DsRed in the osterix-DsRed/TRAP-GFP line, which fluorescence visualizes the early stage of osteoblasts, revealed high expression in the flight group (Fig. 2a–f). To examine the effect of microgravity on the whole-body, we observed overall this transgenic medaka, and found that the intensity of the fluorescent signals was enhanced in the whole-body (Fig. 2g,h). Then, we focused on the pharyngeal bone region, in which bone turnover is high and sensitive to microgravity21, and observed ground and flight samples at high magnification with a 20x lens (Fig. 3a,b) to examine the details of fluorescent signals in osteoblasts. When the fluorescent signal was measured in the pharyngeal bone region including the cleithrum (Fig. 3h), the results revealed that in the flight group, this intensity was increased compared with that in the ground group over the 8-day observation period (Fig. 3c). The signal-positive area was also increased about 8.0 fold or more (Fig. 3d). Next, to examine the late stage of osteoblasts, we measured the intensity and area of DsRed signals in the osteocalcin-DsRed/TRAP-GFP line and found a large increase in intensity in the flight group (Fig. 3e–h); however, no statistically significant increase in area was found (data not shown). To remove any possibility of a contribution of hypergravity exerted during the launch into space to the level of fluorescent signals, we performed a hypergravity experiment, and the results showed no significant alteration of signals (Supplementary Fig. S2). This result suggested that the hypergravity occurring at launch seems to have had no detectable effect on the osterix-DsRed signals.
Increase in the fluorescence intensity in osteoclasts
In osteoclast development, since the larva at stage 39 shows the initial phase for osteoclastogenesis in the pharyngeal bone region, we observed fluorescent signals of larvae at this stage in TRAP-GFP or in MMP9-DsRed fish. MMP9 as well as TRAP14 is a typical marker of osteoclasts in medaka (Supplementary Fig. S3). Our results showed that the intensity of the TRAP-GFP-positive signal was increased at days 4 and 6 after launch in the flight group compared with that in the ground group (Fig. 4a–c), whereas the signal area was not significantly altered (data not shown). The intensity of MMP9-DsRed signals was also increased at days 4 and 6 after launch in the flight group (Fig. 4d–f), though there was no significant alteration of the area (data not shown). Thus the fluorescent signals driven by osteoblast- and osteoclast- specific promoters were enhanced in the flight group. Both RANKL-GFP, which replicates the expression pattern of endogenous RANKL (data not shown), which is the key factor for osteoclast differentiation23, and cox2-GFP24 (data not shown) lines showed no significant difference in the fluorescence intensity between the ground and flight groups (Supplementary Fig. S4).
Co-localization of osteoblasts and osteoclasts under microgravity
The interaction of osteoblasts and osteoclasts is important for bone remodeling. It has been reported that there are many osteoblasts and osteoclasts in pharyngeal bones21, and osteoblasts are important for osteoclastogenesis in these bones15. To study the co-localization of osteoblasts and osteoclasts, we observed osterix-DsRed/TRAP-GFP merged images (Fig. 5). DsRed signals for osteoblasts were enhanced in the flight group, and the GFP signals for osteoclasts localized near osteoblasts were also enhanced during flight (Fig. 5a–d). The TRAP-GFP signals emerged at the lower pharyngeal bone region; and compared with the intensity of the ground control they increased in intensity near the osteoblasts highly expressing osterix in the flight medaka (Fig. 5e–j). Furthermore, we confirmed the localization of GFP and DsRed signals in the pharyngeal bone region in flight medaka by performing three-dimensional (3D) analysis (Fig. 5k–n). Figure 5k shows a 3D image of the distribution of the fluorescent proteins. The pharyngeal bone was localized at the inside of the cleithrum, as shown in Supplementary Fig. S1.
Alteration of bone-related gene expression in the pharyngeal bone region by HiSeq
The results of live-imaging showed the enhancement of fluorescent signals in both osteoblasts and osteoclasts under microgravity. To examine alteration of the gene expression levels in bone tissues, we extracted RNAs from the pharyngeal bone region in medaka juvenile at day 2 after launch. Unfortunately, because the amount of RNAs from small pharyngeal bones was extremely low, the RNAs of individual fish were mixed to perform HiSeq analysis of the flight versus ground group. Our results showed that 2 osteoblast-related genes, col10a1 and osteocalcin, and 3 osteoclast-related genes, acp5 (TRAP), cathepsin K, and MMP9, were significantly up-regulated in the flight group (Table 2). Regarding osterix mRNA, the expression level showed 7.99 fold increase in the flight, though this data showed less statistically importance (data not shown).
GO analysis for gene expression of whole-body medaka in flight by RNA-Seq
To examine the alteration of gene expression levels early in orbit, we focused on the common up- and down-regulated genes in the whole-body at days 2 and 6 after launch. RNA-Seq analysis was performed on total RNAs extracted from the whole-body medaka. We examined over 20,130 (90.3%) and 21,062 (94.5%) expressed genes at days 2 and 6, respectively. With a false-discovery rate (FDR) of <=0.2, 2,958 up-regulated (S > G) genes (13.3% of all genes) and 3,631 down-regulated (S < G) genes (16.3% of all genes) were shown to be differentially expressed genes (DEG) by the RNA-Seq analysis. The number of common genes for up- and down-regulation between days 2 and 6 was 105 and 48, respectively, and categorized according to the following classification: Molecular function, Biological process, and Cellular component (Supplementary Table S3). Figure 6 shows the ratio of enriched GO annotations for up- and down-regulated genes in the “cellular component” in the GO domain. In particular, the GO analysis showed that GO:0005634 (nucleus) was significantly enhanced in up-regulated genes under the microgravity, whereas GO:0005886 (plasma membrane) was significantly enhanced in down-regulated genes.
Up-regulation of the molecules acting in the nucleus
GO analysis showed up-regulation of the molecules that act in the nucleus. Of the 105 genes that were up-regulated in the whole-body medaka at days 2 and 6, 33 genes were specifically found as molecules that act in the nucleus. Thirty-one of these 33 genes were up-regulated at day 2 compared with their expression at day 6, suggesting that enhancement of transcription occurred immediately after exposure to microgravity (Supplementary Table S4). In addition, the gene expression levels of MCM (minichromosome maintenance) family genes, mcm7, mcm5, mcm4, and mcm3 were significantly increased at day 6 (Supplementary Table S5).
Alteration of the gene expression levels of cell-surface molecules
Forty-eight genes were down-regulated in the whole-body medaka at days 2 and 6. Nineteen genes and 29 genes were down-regulated extremely at day 2 and 6, respectively. For the highly down-regulated genes for membrane proteins in the flight group, we classified them into 4 categories of membrane proteins: cell adhesion proteins (7 genes), channel and transporter proteins (3 genes), receptor proteins (2 genes), and membrane-related proteins (12 genes), as shown in Supplementary Table S6. Especially, the solute carrier family and the claudin family were characterized in both up- and down-regulated gene expression profiles: slc13a5 and slc25138A were up-regulated, slc12a3 was down-regulated, claudin-5 was up-regulated, and claudin-7 and claudin-like protein ZF-A89-like were down-regulated (Supplementary Table S6). These findings suggest that the expression levels of slcs and claudins were influenced by gravity.
Up-regulation of molecules in pharyngeal bone tissues and whole-body
To identify the common up-regulated genes related to bone tissues among 105 genes that were up-regulated in the whole-body at days 2 and 6, we examined the overlapped genes in the transcriptome between the pharyngeal bone at day 2 and the whole-body at days 2 and 6. Our results showed that only 5 genes, i.e., jun-B-like and c-fos for the AP-1 family, pai-1 (Plasminogen activator inhibitor type 1), ddit4 (DNA damage-inducible transcript 4 protein), and tsc22d3 (TSC 22 domain family member 3), were found to be significantly up-regulated genes (Table 3).
Under microgravity, there are several changes in the animal body, such as fluid shift, increase in blood pressure, and dizziness. In particular, bone mineral density is decreased under microgravity25; but it is unclear how osteoblasts or osteoclasts respond early in orbit. In spaceflight, there are 2 phases in the adaptation to a specified environment under microgravity; one is the initial extreme alteration from ground 1 G to μG early in orbit, and the other is the adaptation to chronic stress during long-term flight. It is important to understand the initial response; however, previous studies were performed either in vitro or by using artificial microgravity. In our present study, we took 2 approaches, i.e., live imaging and transcriptome analysis, to examine the initial response to microgravity. Especially, the live-imaging analysis is useful to examine real-time alterations of cells under microgravity. We observed living animals (medaka) at the ISS for the first time via remote operation from Tsukuba Space Center, and found by live-imaging that the fluorescent signals of osteoblasts as well as those of osteoclasts were significantly increased over those for the ground control. In the whole-body fish, the osterix-DsRed and osteocalcin-DsRed signals in osteoblasts were increased in intensity, indicating that osteoblasts were directly affected by microgravity regardless of osteoclast commitment.
We propose the following possible mechanism for the up-regulation of osterix, osteocalcin, TRAP, and MMP9 genes under microgravity: Osteoblasts and osteoclasts are located on bones, which are most sensitive to gravity alteration because they are the tissue with the highest density in the body. Bone-specific genes such as osterix and osteocalcin may have properties affording a response to gravity. Both osterix and osteocalcin transcription was up-regulated at the same time: day 1 as shown in the fluorescent intensity. This is different from normal osteoblast differentiation in which osterix and osteocalcin expressions appear at the early and the later stage, respectively, during osteoblast differentiation. At the ISS, this disorder of osteoblasts causes activation of osteoclasts, or osteoclasts may respond directly to the gravity alteration in a different manner, resulting in enhanced expression of TRAP and MMP9 genes.
The transcriptome analysis of pharyngeal bones showed significant up-regulation of 2 osteoblast-related genes and 3 osteoclast-related genes in the flight group: col10a1 and osteocalcin and for the former and acp5 (TRAP), cathepsin, and MMP9 for the latter. Enhanced gene expression of osteocalcin, TRAP, and MMP9 was consistent with the results of the live-imaging study.
Gene ontology analysis using mRNAs from the whole-body fish at days 2 and 6 showed significant up-regulation of genes involved in “nucleus regulation”. Consistently, it has been reported that in parabolic flight experiments performed in vitro, unexpected effects on cells are observed, mainly on molecules related to transcription10. It is considered that cells adapt to a change (microgravity) by rearranging their transcriptional apparatus to counteract alterations in gene expressions as a reaction to a stimulus under microgravity. Among our findings, 2 of them were especially important. Firstly, of the genes involved in regulation of the nucleus, we found that 5 of the 23 nucleus-related genes selected in the whole-body transcriptome analysis were related to osteoblast or osteoclast function, and were up-regulated to a greater extent at day 2 than at day 6. Regarding these 5 genes, klf9 and klf2 are regulated in the macrophage network via the glucocorticoid receptor26, foxa3 is a crucial regulator of hypertrophic chondrocyte differentiation27, maf promotes osteoblast differentiation28, and CCAAT/enhancer-binding protein delta is involved in inflammation29. Secondly, we found that the MCM (minichromosome maintenance complex) family, which is the DNA helicase complex required for DNA replication, was up-regulated at day 6. Especially, mcm3 in osteoblasts was reported to be up-regulated by irradiation30. Taken together, our results demonstrate that cells immediately produce the necessary transcription factors and remodel the chromatin structure in their nucleus. Interestingly, 2 transcription factor genes, gadd45 and klf2, were reportedly up-regulated under hypergravity in the another fish model, zebrafish31; and these 2 genes were also up-regulated under microgravity (Supplementary Table S4). Furthermore, c-fos, jun-B-like, and jun dimerization protein 2-like were also up-regulated under microgravity (Supplementary Table S4); and in a clinorotation study, which is commonly used to compensate for the unilateral effect of gravity, FOS-JUN transcription factors were regulated by the GADD45B factor for their global expression32. Taken together, these findings indicate that there may exist a general mechanism against the gravity.
In the analysis of commonly up-regulated genes in the whole-body fish at days 2 and 6, and in pharyngeal bones at day 2, we found that 5 of them, i.e., c-fos, jun-B-like, pai-1, ddit4, and tsc22d3, were commonly up-regulated. c-Fos and jun-b are immediate early-response genes that include response to alteration of gravity33,34; and among the members of the jun family, junB is quickly activated, as was shown in a clinostat experiment34. This jun member is a part of the inducible transcription factor complex AP-1, which is a positive regulator for controlling the formation of primary osteoblasts and osteoclasts35. Furthermore, TGF-β induces pai-136 and tsc2237,38. Omata et al. reported that c-fos and Smads can activate osteoclasts, in which Smads are involved in the TGF-β signaling pathway39, a pathway potentially activated by mechanical stress.
Previous studies showed that glucocorticoid induces pai-137, ddit440, and tsc22d341 and that the transcription factor AP1 regulates glucocorticoid receptor (GR) binding at the chromatin level42. GRs are possibly involved in osteoclast activation, because GR and AP-1 synergistically activate transcription, in which AP-1 guides GR binding. Pai-1 and Tsc22d3 are activated by the combination of TGF-β and GR26,36,41,43,44, whereas ddit4 is enhanced by GR40. During spaceflight, blood pressure changes early in orbit45,46. It is also known that the stress of elevated blood pressure produces nitric oxide (NO)47 or NO reduces blood pressure48. Recently, it was shown that GR and NO have a synergistic function49; and interestingly, it was reported that stimulation by NO induces tsc22d3, ddit4 and klf250, and that preeclamptic plasma down-regulates klf9, tsc22d3, cebpb, ddit4 and jdp251. In our results, expressions of these genes were altered under microgravity, which thus suggests that NO-GR signaling is related to the “microgravitational stress”. Taken together, available data indicate that the GR is the main molecule involved in the effect of microgravity on cells, consistent with our observations of activation of GRs in medaka fish reared long-term in the ISS21. Finally, to clarify the GR action under microgravity, further analyses are required. We plan to further investigate the function of these genes in our next space experiment.
Double-transgenic medaka lines
MMP9-DsRed line: A 3.2-kb upstream regulatory region of the medaka mmp9 gene was amplified by using the following primers: 5′-GCGAAGCTTCATGTTGCTAAGTCTCAGAGTC-3′ (forward) and 5′-GCGAATTCTTTGAGATCTAATGTGGACTAGTG-3′ (reverse). The amplified fragments were cloned into the TA cloning vector. We then digested the 5′-half fragment with HindIII and EcoRI, and subcloned it into the HindIII/EcoRI site of the I-Sce1 backbone vector, which was subsequently inserted into DsRed-Express/SV40polyA (Clontech) at the HindIII/AflII sites in the pBSKI2 vector (AMAGEN).
RANKL-GFP line: The fosmid clone golwfno356_d02 including the rankl genomic locus was obtained from an ensemble database and NBRP Medaka (https://shigen.nig.ac.jp/medaka/), utilized for homologous recombination with an EGFP-kanamycin cassette by using the protocol previously described52. The EGFP cassette was amplified by using the following primers: 5′-AAGCCTCCAGAGTCCGGGAGCGTGGGGCCGATCCGCACGCGACGCGCGTCTCCACCG GTCGCCAC CATGG-3′ (forward) and 5′-GCGCTCGACAGGCTCCTCGGAGCGCGCGCGCGCGCACAGGCTGCCCTTACGAGGCTATGGCAGGGCCTGC-3′ (reverse). The underlines show the homologous recombination sites. The PCR products were recombined into exon 1 of the medaka rankl gene.
Two space experiments for study of the initial response to microgravity
We performed space experiments twice using medaka fish for the study of the early response to microgravity (Table 1). In 2012, 6 juvenile fish each were preserved by RNAlater at the ISS at days 2 and 6 after launch. In 2014, the fluorescent signals from 24 larvae fish of 4 double transgenic lines were observed at the ISS for in vivo imaging under microgravity.
The experiments were performed in accordance with policies and protocols approved by the Japan Aerospace Exploration Agency (JAXA) Institutional Animal Care and Use Committee. In the experiment at the ISS in 2012, at days 2 and 6 after launch, medaka fish were transported into the “Fish Fixation Apparatus” for analysis of mRNA expression levels. The buffer used in the Fish Fixation Apparatus was RNAlater (Sigma-Aldrich, MO, USA). Specimens were frozen and stored at −95 °C for later mRNA analyses. These specimens were maintained at −95 °C and transported from NASA to Japan.
In the next experiment, medaka larvae were placed in the “Medaka Chamber” and flown on the Soyuz flight TMA-10M (Roscosmos, Russia) in 2014. After arrival at KIBO, which is the space laboratory of Japan in the International Space Station (ISS), the medaka chambers were set under a fluorescence microscope for live imaging for 8 days.
Embedding of medaka larvae for in vivo imaging
Cab, an inbred wild-type strain of the medaka (O. latipes), was used throughout this study. Fish were kept under a photoperiod of 14 h light/10 h darkness at 28 °C. Eggs were obtained and kept at 25–28 °C after collection. After hatching at day 9, larvae were embedded in Mebiol Gel (Mebiol Inc). Mebiol Gel has a unique property; i.e., it is a liquid at a low temperature, but turns into a gel upon being warmed up.
For preparation of the gel solution, 0.5 ppm methylene blue in water including 1% streptomycin and 0.57% penicillin was filtered, after which 12 ml of the solution was added to the Mebiol Gel container. For dissolution, the containers were shaken for 2 days at 4 °C.
Hatching larvae were incubated on ice for 10 minutes for anesthesia, and 12 larvae were lined up on the glass plate of a chamber. Promptly, the chamber was filled with 2.1 ml of gel solution, after which its upper side was covered with a semipermeable membrane. As shown in Supplementary Fig. S1, pharyngeal bones were clearly observed from the ventral side. In this experiment, the ventral side was oriented toward the glass plate for observation via an objective lens (Fig. 1b).
Medaka chamber (#1) contained osterix-DsRed/TRAP-GFP (n = 10) and RANKL-GFP/MMP9-DsRed (n = 2); and Medaka chamber (#2), RANKL-GFP/MMP9-DsRed (n = 3), osteocalcin-DsRed/TRAP-GFP (n = 5), and cox2-GFP/TRAP-DsRed (n = 4). Three chambers including backup samples were prepared for #1 and #2, respectively.
The experiment for the ground control was carried out under the same conditions as used for the flight group.
Microscope Observation System
The Microscope Observation System consisted of a microscope, a power supply, and the control unit containing a VGA-NTSC converter and an Experiment Laptop Terminal (ELT). This system was used to conduct fluorescence observations and also supported live imaging of medaka transgenic lines. We manipulated this system under the same measurement conditions both at ISS and on the ground. During the experiment at the ISS, the crew set up the medaka sample at the ISS, and remote observations and operations were conducted by command from Earth via the ELT (Experiment Laptop Terminal). The recorded image files were transferred back to Earth. The microscope used was an inverted vertical illumination fluorescence microscope (DMI6000B, Leica Microsystems) partially modified to fit the space environment. All microscope operations on the stage, the object lens revolver, the fluorescence filter turret, and the capacitor were controlled electrically53.
Live imaging of medaka fish
Twelve larvae at stage 39 were embedded in one “Medaka Chamber” (Fig. 1a), where larvae in Mebiol gel (Mebiol Inc.) were covered with a gas-permeable membrane to remain alive. The temperature for this experiment was maintained between 19–23 °C. The chambers including fish larvae were shaded all day. The numbers of fish in the flight and ground groups are shown in Supplementary Table S1. The growth of fish in the flight group was similar to that of those in the ground group, and the larvae in both conditions were at stage 39 when they were embedded in the gel.
The microscope used was a modified fluorescence microscope (DMI 6000B, Leica Microscope Systems Co.), which was controlled by a specialized software. This software was able to receive a command from the ground control and execute the microscope’s actions continuously by using a batch process. Fluorescent signals were observed with the filter set and the LED light source optimized for each signal. Collection of images of live larvae in random spatial distribution was performed in 3 steps. In the first step, the XY coordinates of each larva was set approximately by using a 5x objective lens. In the second step, these coordinates were narrowed down; and the Z coordinate was set within the limits of 1000 μm by using a 10x objective lens. The interval of all continuous images was 100 μm in the head region. In the final step, the tack-sharp Z-stack images within the limits of 500 μm were captured by using a 20x lens. The interval of all continuous images was 5 μm in the pharyngeal bone region. These steps were summarized in “Fig. 1”.
In the ground control group, images were captured under the same conditions as used for the flight group, and the temperature was controlled at around 21 °C. We measured fluorescent signals using the same time course on the ground and in the flight. We confirmed that there was no significant difference in the calibration of the microscope by using the background luminance caused by the excitation light for both GFP and DsRed fluorescence. We checked this calibration value by using cox-2-GFP signals at the head of the transgenic line, which showed the constitutive signals and found a similar level of signals in both ISS and the ground (data not shown).
Quantitative analysis of fluorescent signals
The intensity and area of GFP and DsRed signals were calculated by use of ImageJ software (ImageJ). The fluorescent signal area was selected by the process Image/Adjust/Threshold in ImageJ. Adjustment of the parameter in “Threshold” shows the adequate selected area as a “red region” on the window of ImageJ. Next, the intensity and the area were calculated by the process Analyze/Measure (“Limit to threshold” is selected in “Set Measurements”). The fluorescent signal area was cropped by “Polygon sections” when necessary. The captured images during flight were noised as small spots by cosmic rays. These small spots were canceled by removal of outliers (radius: 2.0 pixels, threshold: 50, and bright outliers). The range of each observation was adjusted enough to contain the fluorescence of tissues. The observation of pharyngeal bones in the flight samples covered 101 slices, and that of the ground control, about 55 slices, by focus adjustment with manual operation for the minimum range. The images were stacked in a single file. As described above, we selected the fluorescent signal area and calculated it with the process, Analyze/Histogram, by the measurement of both “area” and “intensity” for all images, which was shown as a stacked file.
Statistics of fluorescent signals
The fluorescent signal data are shown as the mean ± s.e.m. The statistical analysis was performed by the one-way analysis of variance, followed by unpaired Student’s t-test. A P-value < 0.05 was conventionally considered statistically significant.
Analysis for the localization of osteoblasts and osteoclasts
For osterix-DsRed and TRAP-GFP in the pharyngeal bone region, the three-dimensional images of the fluorescent proteins were constructed by using Fiji, an image processing package.
To confirm the effect of hypergravity at launch, we reproduced the hypergravity condition54. The embedded osterix-DsRed transgenic medaka fish in a gel were continuously exposed to 4.3 G for 2 minutes, 2.7 G for 2 minutes 40 seconds, and 3.75 G for 4 minutes 5 seconds. The fluorescent signals for osterix-DsRed were observed before 1 day (day-1), immediately after (day 0), 1 day after (day 1) and 2 days after (day 2) exposure to the hypergravity by using a centrifuge customized for medaka fish (LIX-140SP, Tomy Seiko Co., Ltd). The larvae were kept at 25 °C for the experiment.
Medaka fish were preserved by use of RNAlater at days 2 and 6 after launch into spaceflight in 2012. For flight specimens, RNAs from pharyngeal bones, or whole bodies were extracted at day 2 (n = 4), or at days 2 (n = 3) and 6 (n = 3) after launch. Ground control fish were preserved at Baikonur at day 2 after launch, and RNAs from pharyngeal bones, or whole bodies were extracted as day 2 (n = 10) control, or days 2 (n = 3) and 6 (n = 3) control.
Whole transcriptome analysis by HiSeq
Since a small amount of RNA was extracted from pharyngeal bones at day 2 after launch, flight- and ground- cDNAs were synthesized by using a mixture of RNAs of all extracted samples. The method was followed by the protocol previously reported21.
GO (gene ontology) analysis of whole-body RNA
RNAs from whole bodies were examined by RNA-Seq analysis. The library was of the single-end type. Reads for each condition were mapped to the reference genome. FPKM (fragments per kilobase of exon per million mapped fragments) was calculated for each library, and the difference in FPKM between flight and control groups was compared with consideration of biological duplication. We identified DEGs (differentially expressed genes) by performing the t-test.
Three patterns, day 2 after launch (n = 3), day 6 after launch (n = 3), and both days 2 and 6 (n = 6), were compared with each other; and the replication number was indicated. In confirmation of common or non-common DEG, a candidate DEG was picked up; and then we performed the GO analysis.
Statistics of transcriptome
In the GO analysis, the threshold of p-values in the analysis was set at 0.05. False-discovery rates (FDR) were calculated, and the threshold in the analysis was set at 0.2.
In the gene expression analysis, the threshold of p-values in the analysis was set at 0.05. False-discovery rates (FDR) were calculated and the threshold in the analysis was set at 0.3.
cDNA sequence registration
We registered all RNA-Seq data at the DDBJ (the DNA Data Bank of Japan; http://www.ddbj.nig.ac.jp/). Raw reads of the transcriptome analysis in this study are deposited in the DDBJ Sequence Read Archive under BioProject ID: PRJDB5292.
How to cite this article: Chatani, M. et al. Acute transcriptional up-regulation specific to osteoblasts/osteoclasts in medaka fish immediately after exposure to microgravity. Sci. Rep. 6, 39545; doi: 10.1038/srep39545 (2016).
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We thank Dr. K. Inohaya in Tokyo Institute of Technology for providing the osterix and osteocalcin transgenic lines, Mr. K. Terada in Tokyo Institute of Technology for examining the results of the transcriptome analysis, Ms. M. Hattori in Chiyoda Corporation for embedding of medaka larvae, Mr. T. Sakimura in Japan Space Forum for preparing the medaka chamber, and Dr. R. Kajitani in Tokyo Institute of Technology for registration of sequence data to the DDBJ. We also thank astronauts Mr. K. Wakata in JAXA for setting the medaka chambers for fluorescence microscopy at the ISS. RNAseq libraries constructions and analysis was partially supported by Russian Science Foundation grant for international groups (No. 14-44-00022) work was mainly by grants-in-aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan (grant no. 25514003, 16K15778, 16H01635) and partly by the Ground-based Research Program for Space Utilization promoted by the Japan Space Forum.
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