2026-06-25 · 研究进展Research
非洲爪蟾个体早期发育:卵 → 蝌蚪 → 变态 → 成蛙Xenopus development: egg → tadpole → metamorphosis → adult
非洲爪蟾(Xenopus laevis)体外受精、胚胎数量大、发育迅速且相对透明,是研究脊椎动物早期发育的经典模式动物,对脊椎动物早期胚胎发育研究做出了重要贡献。其发育时期通常采用 Nieuwkoop–Faber(NF)分期系统进行标准化描述。With external fertilization, large clutches and rapid, relatively transparent development, Xenopus laevis is a classic model for vertebrate early development. Stages are standardized using the Nieuwkoop–Faber (NF) system.
受精后,合子经历完全两侧对称型卵裂。第一次卵裂沟为经裂(meridional),第二次同为经裂且与第一次垂直,第三次为纬裂(latitudinal)。由于植物极富含卵黄,动物极形成较小的卵裂球,植物极形成较大的富含卵黄的卵裂球,产生明显的不等裂格局。After fertilization, the zygote undergoes complete bilateral cleavage. The first cleavage furrow is meridional; the second is also meridional but perpendicular to the first; the third is latitudinal. Yolk-rich vegetal cells divide more slowly, producing smaller animal-pole and larger vegetal-pole blastomeres.
约 128 细胞期,胚胎内部形成明显的囊胚腔(blastocoel)。动物极形成小而分裂迅速的细胞,植物极为大型富含卵黄的细胞。晚囊胚期(NF 8–9)启动中囊胚转换(mid-blastula transition,MBT),合子基因组开始转录激活,细胞周期延长并出现不同步。Around the 128-cell stage a distinct blastocoel forms. Animal-pole cells divide rapidly, while vegetal-pole cells remain large and yolk-laden. The mid-blastula transition (MBT, NF 8–9) marks onset of zygotic transcription, cell-cycle lengthening and asynchrony.
推定内胚层细胞向内卷折,在植物极背侧形成狭缝状的胚孔(blastopore)。瓶状细胞(bottle cells)收缩并牵引边缘带细胞内移,最终建立内、中、外三个胚层,并确立背腹与前后体轴。Spemann-Mangold 组织者(organizer)分泌 Chordin、Noggin 等信号分子,拮抗 BMP 通路,诱导背侧中胚层与神经组织。Presumptive endoderm involutes to form a slit-like blastopore on the dorsal vegetal side. Bottle cells constrict and drive internalization of marginal-zone cells, ultimately establishing three germ layers and the body axes. The Spemann–Mangold organizer secretes Chordin, Noggin and related factors that antagonize BMP, inducing dorsal mesoderm and neural tissue.
卵黄栓收缩、胚孔封闭后,脊索结构形成。背侧外胚层增厚成神经板,神经板两侧边缘上卷形成神经褶,最终融合形成神经管与神经嵴细胞,分别发育为中枢神经系统和迁移性颅面及周围神经组织。After yolk plug retraction and blastopore closure, the notochord forms. The dorsal ectoderm thickens into a neural plate; its lateral edges elevate into neural folds that fuse to form the neural tube and neural crest cells, precursors of the CNS and migratory craniofacial/peripheral neural tissues.
体轴形成涉及多个分子调控系统:背侧 Nieuwkoop 中心通过 Wnt/β-Catenin 信号激活脊背基因;各类组织者分泌因子精细调节前后轴与左右不对称。器官原基相继形成,胚胎孵化后进入自由游动的蝌蚪阶段(NF 35 起),开始摄食直至变态为幼蛙。Axis formation involves multiple regulatory systems: the dorsal Nieuwkoop center activates dorsal genes via Wnt/β-catenin; organizer-secreted factors precisely pattern the anterior–posterior and left–right axes. Organ primordia form sequentially; the embryo hatches and begins free-swimming tadpole life (NF 35+), feeding until metamorphosis.
| NF 期NF Stage | 阶段名称Stage | 主要特征Key feature | 温度 20℃ 时约需时间Approx. time at 20 ℃ |
|---|---|---|---|
| 1–3 | 受精 / 卵裂初期Fertilization / early cleavage | 合子 → 8 细胞Zygote → 8-cell | 0–3 h |
| 4–9 | 囊胚Blastula | 囊胚腔、MBTBlastocoel, MBT | 3–8 h |
| 10–12 | 原肠胚Gastrula | 三胚层建立Three germ layers | 8–12 h |
| 13–21 | 神经胚Neurula | 神经管、脊索Neural tube, notochord | 12–20 h |
| 22–35 | 尾芽期Tailbud | 体节、器官原基Somites, organ primordia | 20–48 h |
| 35–46 | 自由游动蝌蚪Free-swimming tadpole | 开口摄食、鳃、心跳Feeding, gills, heartbeat | 2–14 d |
| 47–66 | 变态期Metamorphosis | 四肢、尾部吸收Limb growth, tail resorption | 数月 |
我们按 NF 分期提供不同发育时期的蝌蚪与胚胎材料,并可开展早期胚胎单细胞提取与发育毒性实验。We supply staged tadpoles/embryos by NF stage, and offer single-cell isolation and developmental toxicity testing.