In ovo serial skeletal muscle diffusion tractography of the developing chick embryo using DTI: feasibility and correlation with histology
© Zhou et al.; licensee BioMed Central Ltd. 2012
Received: 9 June 2012
Accepted: 14 December 2012
Published: 26 December 2012
Magnetic resonance imaging is a noninvasive method of evaluating embryonic development. Diffusion tensor imaging (DTI), based on the directional diffusivity of water molecules, is an established method of evaluating tissue structure. Yet embryonic motion degrades the in vivo acquisition of long-duration DTI. We used a dual-cooling technique to avoid motion artifact and aimed to investigate whether DTI can be used to monitor chick embryonic skeletal muscle development in ovo, and to investigate the correlation between quantitative DTI parameters fractional anisotropy (FA) and fiber length and quantitative histologic parameters fiber area percentage (FiberArea%) and limb length.
From 84 normally developing chick embryos, 5 were randomly chosen each day from incubation days 5 to 18 and scanned using 3.0 Tesla magnetic resonance imaging. A dual-cooling technique is used before and during imaging. Eggs were cracked for making histological specimen after imaging. 3 eggs were serially imaged from days 5 to 18. We show that skeletal muscle fibers can be tracked in hind limb in DTI beginning with incubation day 8. Our data shows a good positive correlation between quantitative DTI and histologic parameters (FA vs FiberArea%: r= 0.943, p<0.0001; Fiber_length vs Limb_length: r=0.974, p<0.0001). The result of tracked fibers in DTI during incubation corresponds to the development of chick embryonic skeletal muscle as reported in the literature.
Diffusion tensor imaging can provide a noninvasive means of evaluating skeletal muscle development in ovo.
KeywordsMagnetic resonance imaging Diffusion tensor imaging Skeletal muscle Chick embryo
Animal models play a central role and are essential to basic medical research. Having an established pedigree of use in developmental biology, transplantation research, and cancer research, the chick embryo provides an in vivo model which is both accessible and economical, as it contains all components necessary for development, excepting heat and oxygen . Pluripotent stem cells lines have been derived from various sources, including chicken . Using molecular methods to identify and characterize cell surface markers and enzymatic activity, evaluation of the stem cell differentiation process is an essential step towards successful therapeutic use . Most molecular imaging methods, and traditional imaging methods such as microscopy, require embryonic sacrifice for ex vivo analysis. Magnetic resonance imaging (MRI) allows embryonic imaging without sacrifice, and has been used in avian embryo analysis, primarily for evaluating anatomy [4–8]. Advanced MRI techniques, for example, diffusion-weighted imaging (DWI), diffusion tensor imaging (DTI), magnetic resonance spectroscopy, and blood-oxygen level dependent imaging (BOLD) can be used to obtain structural, metabolic, and functional information in addition to anatomic information [9, 10]. However, anatomic imaging techniques and, in particular, advanced imaging techniques are challenging to implement in embryonic models due to embryonic motion [5, 6, 10].
Diffusion tensor imaging (DTI) is a method of observing the displacement distribution of water molecules present within an imaging voxel, allowing evaluation of tissue structure at a scale below the spatial resolution of MRI . Fractional anisotropy (FA) is a DTI-derived measurement of tissue structural anisotropy ranging from 0 to 1. If the diffusion is isotropic (e.g., unrestricted, like a drop of ink diffusing in the water), the FA value is 0. If the diffusion is along a single axis (like a drop of water diffusing along a line), the FA value is 1. Tracked fiber length is another DTI-derived measurement which represents the average length of a tracked fiber-like tissue structure. Evaluation of the displacement distribution provides insight into the structure and organization of tissues, and DTI is an established method of studying the microstructure of neural tissue and skeletal muscle . A disadvantage of DTI for in ovo imaging use is the long imaging duration and consequent data degradation due to subject motion. Previous work has shown that MR anatomic imaging, including real-time cardiac imaging using rapid sequence imaging, is possible with embryonic anesthesia [6–8, 10]. More recently, it has been shown that cooling chick embryo from incubation day 12 prior to MR imaging allows noninvasive assessment by reducing motion artifact, without significantly affecting normal development . The purpose of this study is to show that DTI can be used to monitor the development of skeletal muscle in chick embryonic hind limb using a dual-cooling technique, and investigate whether serial skeletal muscle tractography in DTI correlates with ex vivo histology from day 8 of incubation through hatching.
Skeletal muscle FA, length of tracked fibers, length of hind limb and FiberArea% values for chick embryonic hind limb at each day of incubation
FA ± s.d.
FiberArea% ± s.d.
0.119 ± 0.009
0.465 ± 0.032
0.138 ± 0.018
0.516 ± 0.029
0.159 ± 0.024
0.561 ± 0.008
0.228 ± 0.039
6.542 ± 0.425
0.605 ± 0.015
0.275 ± 0.026
6.708 ± 0.429
0.631 ± 0.015
0.284 ± 0.073
8.258 ± 0.829
0.667 ± 0.016
0.338 ± 0.019
9.654 ± 0.425
0.698 ± 0.013
0.366 ± 0.019
10.502 ± 0.585
0.718 ± 0.008
0.431 ± 0.024
11.236 ± 0.308
0.729 ± 0.014
0.474 ± 0.025
12.110 ± 0.611
0.757 ± 0.006
0.501 ± 0.044
14.266 ± 0.381
0.776 ± 0.012
0.511 ± 0.037
15.094 ± 0.769
0.814 ± 0.013
0.523 ± 0.047
16.576 ± 1.078
0.844 ± 0.021
0.573 ± 0.088
21.828 ± 1.454
0.867 ± 0.013
Y1 = −0.070 + 0.037 X
Y2 = −5.331 + 1.339 X
Y3 = 0.357 + 0.029 X
Y4= −10.999+ 2.084 X
Our data show that DTI reflects skeletal muscle fiber formation and growth in hind limb during the incubation period. In contrast to invasive methods of analysis, repeated observations on a single embryo throughout incubation can be implemented using DTI and subsequent phenotypic characteristics would be evident at hatching.
Chick embryo skeletal muscle development has been investigated in detail by developmental biologists [13–15]. Multinucleated skeletal myofibers which contain cross-striated myofibrils are formed by the cytoplasmic fusion of mononucleated myoblasts. The myogenic precursor cells delaminate from dermatomyotome of the paraxial mesoderm and migrate to the limb bud, which then proliferate and differentiate into myoblasts. Embryonic myoblasts, which are most abundant on day 5 and disappear on days 7–8, have short fibers and contain few (2 to 3) nuclei; these were unable to be tracked with DTI in this study. Myoblast fiber length and density increase as embryonic myoblasts mature into fetal myoblasts (peaking at days 8–12) which contain hundreds of nuclei, and then later mature into adult myoblasts prior to hatching[14, 16, 17]. Adult myoblasts located below the basal lamina of adult muscle appear at the late fetal stage and can be activated to divide, differentiate, and form new muscle fibers following injury in postnatal life [16, 17]. DTI tracking of fetal and adult stage myoblasts was successful, and progressive increase in myofibril length is evident on fiber tracking images.
The tracked fiber length of the hind limb in DTI was not entirely consistent with the length of hind limb. For this study, we used a simple measurement method, the length of tracked fibers, which is an average value and it is affected by the tractography stopping threshold parameters (minimum FA, maximum angle change, and minimum fiber length). Therefore, while the DTI measured tracking lengths are not necessarily representative of a single myofiber, it can be considered to be a useful relative surrogate given the correlation obtained between Fiber_length and Limb_length.
This study has several limitations. The spatial resolution of 3.0 T MRI limits evaluation of small embryonic structures, particularly during the early incubation period (before 5 days); spatial resolution would almost certainly be improved with a higher field strength magnet. Matching of MRI imaging planes and histologic specimens was performed with careful attention to detail but acquiring exact matches is technically challenging and exact matching was not feasible in all cases. The reverse method, used by some researches, would be to use reconstructions of the isotropic or nearly-isotropic 3D MRI dataset to match the histological sections, possibly obtaining more accurate imaging-histologic correlation. Our dual-cooling method, which reduced the temperature, may influence diffusion measurements (such as apparent diffusion coefficient and mean diffusion) compared to room temperature; we intend to explore this possibility in our next work. Furthermore, there may be developmental differences among embryos of the same incubation day, though this could be accounted for by increasing statistical power.
Given that DTI has the ability to evaluate skeletal muscle differentiation and development, it may be possible to monitor the effect of mutations which affect skeletal muscle migration and development [18, 19]. DTI also has the potential to observe the embryonic development of other fiber-like tissues, such as smooth muscle, myocardium and nerves. In particular, DTI has the potential to provide information about white-matter tract integrity within the developing brain and spinal cord. For example, regional dysmyelination effects were able to be measured with DTI within shiverer mouse mutant brain tissue , and DTI diffusion parameters showed changes in rodent spinal cords receiving moderate T7 level injury . Similar effects may be possible to measure within the chick embryo.
In conclusion, this study shows that a widely-available (3.0 T) MRI system can be used as a powerful investigative tool to evaluate embryonic development with diffusion tensor imaging in ovo from 5 days incubation to hatching. We show that acquired skeletal muscle diffusion tensor imaging parameters correlate with histologic specimens from sacrificed embryos. Noninvasive evaluation of developmental processes in embryonic models has traditionally been technically difficult and largely restricted to anatomic evaluation. Functional imaging with DTI MRI and other advanced MRI techniques permit the evaluation of tissues and cellular processes below the conventional spatial resolution of MRI, and is a potentially promising method of improving the understanding of early developmental processes.
Animals and treatments
The experimental protocol and procedures were approved by the Institutional Ethics Committee of the Shanghai Jiaotong University School of Medicine. Ninety (90) fertile Hy-Line White eggs each weighing 50–55 g were obtained from a commercial hatchery and placed in a digital tabletop incubator with temperature (37.8°C) and humidity (60%) controlled automatically. After four days of incubation, eggs were “candled” (using a hand-held light source, light was shone through the egg) to determine if they were fertile and developing normally. Six eggs were removed from the incubator for underdevelopment. From the 84 remaining eggs, 5 eggs were chosen at random each day, from incubation day 5 to 18 (14 days total). Eggs were first removed from the incubator and air-cooled for one hour at 3.5-4°C prior to imaging. The surface temperature of the egg before air-cooling was 24-26°C. During imaging, the egg was wrapped in a single piece of Techni-Ice (Techni Ice, Victoria, Australia). Techni Ice egg-contact surface temperature was 0-2°C, as measured immediately prior to and after imaging. Temperature monitoring during imaging was not performed. The dual-cooling method was used to suppress embryonic motion throughout the imaging session (about 32 minutes). In order to show the in ovo serial skeletal muscle diffusion tractography of the developing chick embryo using DTI, an additional 3 eggs were imaged serially without making histological specimen from day 5 to 18.
MR Image acquisition
Eggs wrapped in Techni-Ice were imaged in a 3 T Philips Achieva (Philips Medical Systems, Best, Netherlands) using a four-channel dedicated animal coil with a 5 cm inner diameter. Image acquisition consisted of high-resolution T2 weighted SENSE TSE (turbo spin echo) images (accelerated with SENSE, TR/TE=4375/80 ms, FOV 50 × 45 × 42 mm, ETL=13, NEX=10, matrix 250 × 225 (0.2 × 0.2 mm), slice thickness 1.2 mm, no gap, 12 min 23 s duration), and SENSE DTI using SE (spin echo)-DWI (15 directions, TR/TE=5517/65 ms, FOV 50 × 45 × 42 mm, matrix=83 × 75 (0.6 × 0.6 mm), b=500 s/mm2, NEX=2, slice thickness 1.2 mm, no gap, 20 minute duration). A 16th unweighted (b=0) DTI image was also acquired. All imaging planes were sagittal.
MR fiber tracking
Skeletal muscle fibers in the hind limb were tracked using FiberTrak software (Philips Medical Systems, Best, Netherlands). Three parameters, minimum fractional anisotropy (FA), maximum angle change, and minimum fiber length needed to be set to determine the stopping threshold of tractography. We chose a small minimum FA (0.15) and small maximum angle change (27°) to balance the sensitivity of myofiber tracking during early development stage and the precision during later development; these values were held constant throughout the incubation period. Small values for minimum fiber length (5 mm) were used during early incubation (days 5–11), and minimum fiber length was increased to 10 mm during later incubation (days 12–18).
Data management and statistical analysis was performed using MedCalc (MedCalc Software, Mariakerke, Belgium). A linear model was used to evaluate the relationship between day of incubation and ROI-derived fractional anisotropy (FA) values, length of tracked fibers, FiberArea% and length of hind limb. To evaluate the relationship between imaging and histology during embryonic development, two correlation analyses were performed with p values < 0.05 considered to be significant. One was between FA and FiberArea%, the other was between length of tracked fibers (Fiber_length) and length of hind limb (Limb_length).
Magnetic resonance imaging
Diffusion tensor imaging
Region of interest
The percentage of skeletal muscle Fiber within a given histologic specimen.
E.M.H and JN.H acknowledge support from the Wayne State University Perinatal Research Imaging Initiative. This research was supported by the National Natural Science Foundation of China (No. 81171325), Shanghai Science and Technology Committee Medical Guide Project (No. 114119a0900) and Shanghai Leading Academic Discipline Project (Project No. S30203).
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