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この記事について

  • 要約
  • 要約
  • 概要
  • プロトコル
  • 結果
  • ディスカッション
  • 開示事項
  • 謝辞
  • 資料
  • 参考文献
  • 転載および許可

要約

長い波長多光子蛍光励起顕微鏡レーザーの高度な光学技術の組み合わせは、Tg (sox10:EGFP) および Tg (foxd3:GFP) ゼブラフィッシュ胚の神経堤移行の高解像度、リアルタイム三次元画像をキャプチャする実装されました。

要約

先天性の目と頭蓋顔面の異常、神経の頂上、全身に様々 な細胞タイプに上昇を与える渡り鳥の幹細胞の一時的な人口の混乱を反映します。神経の頂上の生物学を理解することは、制限、リアルタイムで生体内で調査することができます遺伝的扱いモデルの不足を反映してされています。ゼブラフィッシュは、渡り鳥細胞群、神経堤などを勉強するため特に重要な発達モデルです。Sox10とfoxd3初期神経分化と神経堤細胞のマーカーを表す可能性があります多数の動物モデルで示されている、発展途上の目に神経の頂上の移行を検討するには、長波長多光子蛍光励起顕微鏡レーザーの高度な光学技術の組み合わせはトランスジェニックゼブラフィッシュ胚で、Tg (sox10:EGFP) と Tg (foxd3:GFP)、すなわち開発の目の高解像度、立体化、リアルタイムのビデオをキャプチャする実装されました。多光子タイムラプス イメージングは、動作や目の早期開発に貢献する 2 つの神経堤細胞集団の移住性パターンを識別する使用されました。このプロトコルは、例としてゼブラフィッシュ神経堤移行中に時間経過のビデオを生成するための情報を提供し、ゼブラフィッシュと他のモデル有機体の多くの構造の初期の開発を視覚化するさらに適用することができます。

概要

先天性眼疾患小児失明を引き起こすことができるおよび頭蓋神経堤の異常によることが多い。神経堤細胞は神経管から発生し、全身の多くの組織を形成する非定常の幹細胞です。1,2,3,4,5前と、中脳由来神経堤細胞は、骨と軟骨の顔面と前頭葉、虹彩、角膜、小柱網と目の眼の強膜に上昇を与えます。4,6,7,8神経堤細胞、咽頭アーチ菱フォーム、あご及び心臓流出路から。1,3,4,9,10研究を強調しますしている眼に神経の頂上の貢献や眼周囲の開発、脊椎動物の目の開発のこれらのセルの重要性を強調します。確かに、神経堤細胞の移動と分化の混乱は、Axenfeld リーガー症候群および Peters プラス症候群における顎顔面と眼球の異常に します。11,12,13,14,15,16,17したがって、これら神経堤細胞の分化、増殖、移行の包括的な理解は、先天性眼疾患の基になる複雑さに洞察を提供します。

ゼブラフィッシュはゼブラフィッシュ眼の構造は、哺乳類に類似し、多くの遺伝子は、ゼブラフィッシュと哺乳類の間保存された眼の開発を研究するため強力なモデル生物です。18,19,20また、zebrafish の胚が透明で、卵生、目におけるリアルタイムの可視化を促進します。

以前に発行された仕事で拡大して、6、7,20神経堤細胞の移動パターン多光子蛍光タイムラプス イメージング (性決定領域 Y) sry 遺伝子の転写制御の下で緑色蛍光タンパク質 (GFP) の付いたトランスジェニックゼブラフィッシュ線を使用して記述された-ボックス 10 (sox10) またはフォーク ヘッド ボックス D3 (foxd3) 遺伝子の規定する領域。21,22,23,24. 多光子蛍光タイムラプス イメージングはレーザ走査型顕微鏡標本 fluorophores が付いているタグの立体化、高解像度の画像をキャプチャする長い波長多光子蛍光励起の高度な光学技術を組み合わせた強力な手法です。25,26,27多光子レーザーの使用増加組織浸透と減少蛍光漂白などを含む標準の共焦点顕微鏡上の明確な利点があります。

このメソッドを使用すると、移行と渡り鳥の経路のタイミングでさまざまな神経堤細胞の 2 つの異なる集団が眼周囲間充織と発展途上の目で判別、すなわち foxd3 陽性の神経堤細胞と顔面の間充織で sox10 陽性神経堤細胞。この方法では、開発中にリアルタイムで規制の神経堤の移行を観察しやすくゼブラフィッシュ眼と顔面神経の頂上の移行の移行を可視化へのアプローチは導入されました。

このプロトコルは、Tg (sox10:EGFP) の例として、Tg (foxd3:GFP) 遺伝子導入ゼブラフィッシュ初期の目の開発の間に時間経過のビデオを生成するための情報を提供します。このプロトコルは、ゼブラフィッシュ神経堤細胞由来眼と顔面の構造体の早い開発の高解像度、リアルタイム 3次元可視化のためさらに適用できます。また、このメソッドは、他の組織や臓器ゼブラフィッシュと他の動物モデルの開発の可視化のためさらに適用できます。

プロトコル

The protocol described here was performed in accordance with the guidelines for the humane treatment of laboratory animals established by the University of Michigan Committee on the Use and Care of Animals (UCUCA).

1. Embryo Collection for Time-lapse Imaging

  1. Between 3 and 9 pm, set up male and female adult Tg(sox10:EGFP) or Tg(foxd3:GFP) transgenic zebrafish in a divided breeding tank for pairwise mating.
    NOTE: The Tg(sox10:EGFP) and Tg(foxd3:GFP) fish, kind gifts from Thomas Schilling and Mary Halloran, respectively, were crossed into the Casper (roy -/-, nacre -/-) background to decrease auto-fluorescence and interference with pigmentation.
    1. Assemble the breeding tank (slotted inner tank + solid outer tank) and fill it with reverse osmosis (RO) system water.
    2. Transfer up to 3 females and 3 males into opposing sides of the tank separated by a divider; up to 6 fish can be bred pairwise in a single breeding tank.
    3. The next morning, remove the divider shortly after the lights turn on in the vivarium.
      NOTE: In the present study, the lights are on a 14-hour light (on at 9 am) and 10-hour dark (off at 11 pm) cycle.
    4. Allow undisturbed mating for 20 min or until sufficient numbers of embryos are produced; the embryos will be at the bottom of the breeding tank. When eggs are observed, lift the slotted inner tank out along with the fish and quickly place them (fish and inner tank) into a clean solid outer tank filled with RO water.
  2. Prepare standard 1X embryo medium by adding the following per 1 L of RO water: 0.287 g (4.9 mM) NaCl, 0.127 g (0.17 mM) KCl, 0.048 g (0.33 mM) CaCl2.2H2O, 0.04 g (0.33 mM) MgSO4 (anhydrous). Stir solution until the salts are completely dissolved.
    1. Add 100 µL of 0.1% methylene blue as a fungicide. Add 0.25 g of sodium bicarbonate to adjust the pH to 7.75. Store medium at room temperature.
  3. Collect eggs from the outer tank using an egg-collecting screen, and transfer the eggs to Petri dishes (~50 embryos per dish) containing 30 mL of 1X embryo medium. Incubate the collected eggs at 28.5 °C.
  4. Embryo preparation
    1. Tg(sox10:EGFP) embryos.
      1. For Tg(sox10:EGFP) embryos, at 12 h post-fertilization (hpf), remove the dead eggs and assess the developmental stage of the embryos. Screen for GFP-positive embryos using a dissecting fluorescent stereomicroscope with a standard 460-490 nm band-pass excitation filter. Using forceps, remove the chorions from 3-4 embryos that express GFP, and transfer these embryos to a separate Petri dish containing 30 mL of fresh 1X embryo medium.
    2. Tg(foxd3:GFP) embryos.
      1. For Tg(foxd3:GFP) embryos, at 22-24 hpf, remove the dead eggs and assess the developmental stage of the embryos. Screen for positive embryos using a dissecting fluorescent stereomicroscope with a standard 460-490 nm band-pass excitation filter. Using forceps, remove the chorions from 3-4 embryos that express GFP.
      2. Prepare 1000X Phenylthiourea (PTU) stock solution by dissolving 0.75 g (3%) of PTU in 25 mL of Dimethylsulfoxide (DMSO). Aliquot and store the stock solution at 4 °C. Add 30 µL of 1000X PTU (3%) stock solution to 30 mL of 1X embryo medium to generate 0.003% PTU solution.
      3. Place the screened and dechorionated GFP-positive embryos in 0.003% PTU solution to inhibit pigmentation. Do not initiate treatment of the embryos with PTU prior to 20 hpf, as early treatment (at <20 hpf) can have adverse effects on neural crest and neuroepithelial development.28
    3. Prior to conducting the time-lapse experiment, monitor the embryos through live imaging using a standard stereomicroscope at 12-24 h intervals in age-matched comparisons as a control for temperature drift.

2. Mounting of Embryo for Time-lapse Imaging

  1. Preparation of time-lapse embryo media
    1. Prepare standard 0.4% tricaine stock solution by adding 0.004 g of tricaine to 100 mL of RO water. Aliquot (~1 mL) the stock solution into fresh 1.5-mL centrifuge tubes and store at -20 °C.
    2. Prepare time-lapse embryo medium (50 mL of 1X embryo medium, 0.016% tricaine) by adding 2 mL of 0.4% tricaine solution to 48 mL of 1X embryo medium. If using embryos >22 hpf, then also add 50 µL of 3% PTU stock solution (final concentration.003% PTU) to the embryo medium.
  2. Preparation of 2% low-melt agarose
    1. Add 0.4 g of low-melt agarose powder to 20 mL of 1X embryo medium. Heat for 1-2 min or until the solution is clear and all particles are dissolved.
      NOTE: Increasing the percentage of the agarose gel decreases the porosity of the matrix, which may physically impede the growth and development of the embryo. Therefore, the agarose solution can be lowered to 1.5% to minimize these effects. However, when the excitation beam is held stationary during laser-scanning microscopy, greater heating can occur, increasing rapidly in a logarithmic relationship with time. In this protocol, heating due to fluorophore absorption is highly localized to the focal region. Thus, in the region of interest, the temperature could increase to a value high enough (≥ 30 °C) to melt agarose solutions made at percentages lower than 1.5, thereby directly exposing the embryo to the laser or enabling conditions in which the embryo floats out of the focal plane. For this reason, the use of agarose solutions lower than 1.5% is not recommended.
    2. Aliquot (~1 mL) the agarose solution into fresh 1.5-mL centrifuge tubes for storage. Store excess agarose solution in liquid form on a heat block (60-70 °C) for 2-3 weeks.
  3. Mounting the Embryo
    1. To set up the open bath chamber, place a small amount of high vacuum grease on the base of the open bath chamber. Place a circular glass coverslip onto the base and screw the top of the open bath chamber onto the base until tight ( Figure 1A, B).
    2. Pipet (~500-700 µL) of 2% agarose solution (60-70 °C) into the open bath chamber until the base is ~3/4 filled ( Figure 1C). Note that once the agarose solution is in the open bath chamber on the lab bench, the temperature of the solution decreases approximately 1 °C/s.
    3. Wait 30 s to allow the agarose to cool slightly (~30-40 °C), without completely polymerizing, and subsequently transfer a single embryo to the center of the base ( Figure 1D, E).
    4. Under a fluorescent stereomicroscope, position the embryo using a 1-10 µL micropipette tip, making sure that the embryo is placed near the bottom of the agarose, as the embryo may float away when covered with embryo media if it is placed too near the surface of the agarose.
      NOTE: In the presented videos (Videos 1-3), the embryos are oriented laterally, but depending on the area of interest, the embryos can be oriented ventrally or dorsally.
    5. Monitor and reposition the embryo until the agarose has set. Once the agarose has set, use a transfer pipet to fill the assembled open chamber entirely with time-lapse embryo media ( Figure 1F).
    6. Place the open bath chamber in the quick exchange platform, which fits onto the stage adapter ( Figure 1G). Place the entire setup (embryo, open bath chamber, quick exchange platform and stage adaptor) onto the stage of the microscope immediately above the condenser ( Figure 1H).

3. Microscope Set-up for Time-lapse Imaging

  1. Determining laser settings
    1. Determining laser wavelength to use. Use a wavelength that is twice the excitation wavelength of the fluorophore of interest (e.g. wavelength between 880 and 940 nm for GFP).
      NOTE: In the present study, the wavelength setting for GFP was between 880 and 940 nm. The higher the wavelength, the lower the output power of the laser.
    2. Determine laser transmission. A high percent of laser transmission will kill the embryo, use the lowest level of transmission (recommended). For 24 to 48 h time-lapse studies, as presented herein, keep transmission below 5%.
    3. Determine microscope detection systems and ensure that the correct filters for the fluorophore are in place.
      NOTE: For multi-photon microscopes, there are multiple detection systems with various sensitivities for the emitted fluorescence. In general, an internal detection system has less sensitivity than an external detection system. For transgenic lines with high levels of GFP expression, the internal detection system is adequate. For transgenic lines with low levels of GFP expression or with other fluorophores (e.g., red fluorescent protein), an external detection system may be required to maintain the percent of laser transmission at a reasonable level. Regardless the detection system used, the correct filters for the fluorophore must be in place.
  2. Adjusting software settings on the multi-photon microscope
    1. Using the 5X objective, locate the embryo. Manually raise the stage to the highest position, and use the fine focus to position the embryo in the middle of the microscope range.
    2. Manually lower the stage, and change the 5X objective to the 25X water immersion objective (numerical aperture NA, 0.95). Carefully raise the stage to bring the embryo back into focus.
    3. In the software, click on the "xyzt" mode for obtaining multiple images at time intervals (t) in the x-y plane over a depth of "z". Use the epifluorescence or brightfield view to find the depth of focus in the area of interest, which will demarcate the Z-stack.
      1. In the software, click on "begin" button; for these experiments, the lateral edge of the eye was the beginning of the Z-stack. Click on "end" button; the midline of the embryo was the end of the Z-stack.
        NOTE: The step size was 0.3-0.6 µm and there was a total of ~200 steps for a z-stack size of 60 to 120 µm).
    4. Click on the menu for adjusting acquisition time and imaging frequency. For the present system, ~200 steps requires approximately 5 min for each z-stack acquisition. For adequate recovery of the fluorophore and survival of the embryo, allow for a ratio of at least 1:3 between z-stack acquisition (laser power on) and recovery time (laser power off).
      NOTE: For example, z-stacks are acquired every 20 min with 5 min of z-stack acquisition and 15 min of recovery. For this protocol, larger z-stacks can be obtained, but would appropriately increase the time between z-stack acquisitions, resulting in fewer images over the time-lapse course.
      1. With appropriate time for embryo recovery, set the time between z-stacks in the designated window. Set the total length of time for the experiment in the appropriate window.
    5. Final software, laser, and embryo adjustments.
      1. Turn on the live image setting to make final adjustments to the laser settings. Adjust laser transmission (see 3.1.2), gain and offset slider bars within the software to optimize the fluorescent image. Also, adjust the orientation of the embryo, as needed, depending on the length of the experiment, anticipated growth of the embryo, etc. Make sure that the area of interest remains within the frame through the duration of the experiment.
      2. Turn off the epifluorescent light source as it is no longer needed during time-lapse acquisition. Cover the stage with the laser safety box ( Figure 1I). When using the internal detection system, the laser safety box is adequate for protection against background light. Press "start".
        NOTE: However, with more sensitive external detection systems, the laser safety box does not block enough background light, and additional covers are required to prevent the disruption of image acquisition.

4. During Time-lapse Acquisition

  1. Refill the open bath chamber with time-lapse embryo media every 8-12 h (at least 2 times per day) during time-lapse acquisition through the sliding doors on the laser safety box ( Figure 1I).
  2. Before opening the doors of the laser safety box, ensure that the microscope is not actively acquiring an image.
    NOTE: The use of heaters and circulating media systems is not necessary for time-lapse imaging experiments lasting 24 to 48 h. Indeed, the temperatures of both stage and in-line heaters are difficult to control, and during image acquisition the embryo exhibits an adequate development rate at a temperature range from 25-28 °C. Moreover, circulating media systems tend to overflow and potentially damage the equipment. Thus, all embryos are routinely staged post-acquisition.

5. Post-acquisition processing

  1. In the software, click on the "file" menu and choose "save".
  2. Open the file in image processing software (see the Table of Materials). Highlight the correct image series. In the software, choose the "Process" menu. Click on 3D Deconvolution and "Apply" to deconvolve each z-stack.
    NOTE: The file is large; therefore, this step may take many hours.
  3. In the software, under the "Process" menu, click on "maximum projection." Click on "Apply" to initiate maximum projection to generate 1 image per z-stack. Export each maximum projected file (1 image per z-stack) as a tiff.
  4. Import individual tiff files into video processing software. Select all tiff files and drag them into the video editor. Adjust length of each image within the video to 0.1s. Export video as mov or mp4 file.

結果

多光子蛍光タイムラプス イメージングは、ゼブラフィッシュ行 craniofacial 構造と Tg (sox10:EGFP) と Tg (foxd3:GFP) の眼の前眼部に上昇を与える頭部神経堤細胞の移行パターンを明らかにしたビデオのシリーズを生成されます。例としてsox1012 と 30 の hpf の間肯定的な神経堤細胞は神経管の端から顎顔面領域 (ビデオ 1 図 2

ディスカッション

多光子タイムラプス イメージングが一過性と渡り鳥の細胞集団の生体内で追跡を可能にします。リアルタイムで萌芽期のプロセスを研究するこの強力な技術を使用ことができます、現在の研究では、このメソッドの結果は神経堤細胞の移動と開発の現在の知識を強化します。以前のタイムラプス イメージング研究は、通常、共焦点レーザ走査型顕微鏡を利用します。29

開示事項

この仕事は健康の国民の協会 (K08EY022912-01) とビジョン研究コア (P30 EY007003) の国立眼研究所からの助成金によって財政上支えられます。

謝辞

著者は、トーマス ・ シリングが親切贈与 Tg (sox10:eGFP) 魚とメアリー halloran さん親切贈与 Tg(foxd3:GFP)魚をありがちましょう。

資料

NameCompanyCatalog NumberComments
Breeding Tanks with DividersAquaneeringZHCT100Crossing Tank Set (1.0-liter) Clear Polycarbonate with Lid and Insert
M205 FA Combi-ScopeLeica Microsystems CMS GmbHStereofluorescence Microscope - FusionOptics and TripleBeam
Sodium ChlorideMillipore (EMD)7760-5KGDouble PE sack. CAS No. 7647-14-5, EC Number 231-598-3
Potassium ChlorideMillipore (EMD)1049380500Potassium chloride 99.999 Suprapur. CAS No. 7447-40-7, EC Number 231-211-8.
Calcium Chloride DihydrateFisher ScientificC79-500Poly bottle; 500 g. CAS No. 10035-04-8
Magnesium Sulfate (Anhydrous)Millipore (EMD)MX0075-1Poly bottle; 500 g. CAS No. 7487-88-9, EC Number 231-298-2
Methylene BlueMillipore (EMD)284-12Glass bottle; 25 g. Powder, Certified Biological Stain
Sodium BicarbonateMillipore (EMD)SX0320-1Poly bottle; 500 g. Powder, GR ACS. CAS No. 144-55-8, EC Number 205-633-8
N-PhenylthioureaSigmaP7629-25G>98%. CAS Number 103-85-5, EC Number 203-151-2
DimethylsulfoxideSigmaD8418-500MLMolecular Biology grade. CAS Number 67-68-5, EC Number 200-664-3
Tricaine MethanesulfonateWestern Chemical Inc.MS222Tricaine-S
Low-Melt AgaroseISC BioexpressE-3112-25GeneMate Sieve GQA Low Melt Agarose, 25 g
Open Bath ChamberWarner InstrumentsRC-40HPHigh Profile
Glass CoverslipsFisher Scientific12-545-102Circle cover glass. 25 mm diameter
High Vacuum GreaseFisher Scientific14-635-5C2.0-lb. tube. DOW CORNING CORPORATION
1658832
Quick Exchange PlatformWarner InstrumentsQE-135 mm
Stage AdapterWarner InstrumentsSA-20LZ-AL16.5 x 10 cm
TC SP5 MP multi-photon microscopeLeica Microsystems CMS GmbH
Mai Tai DeepSee Ti-Sapphire LaserSpectraPhysics
Laser Safety BoxLeica Microsystems CMS GmbH
Leica Application Suite X (LAS X)  SoftwareLeica Microsystems CMS GmbH
Photoshop CS 6 Version 13.0 x64 SoftwareAdobe
iMovie Version 10.1.4 SoftwareApple

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