Cheng Gang, Marotte Lauren R, Mai Jürgen K, Ashwell Ken W S
Department of Anatomy, School of Medical Sciences, The University of New South Wales, 2052 New South Wales, Australia.
J Comp Neurol. 2002 Nov 11;453(2):199-215. doi: 10.1002/cne.10395.
We have studied the development of the hypothalamus of an Australian marsupial, the tammar wallaby (Macropus eugenii), to provide an initial anatomic framework for future research on the developing hypothalamus of diprotodontid metatheria. Cytoarchitectural (hematoxylin and eosin), immunohistochemical (CD 15 and growth associated protein, GAP-43), tritiated thymidine autoradiography, and carbocyanine dye tracing techniques were applied. Until 12 days after birth (P12), the developing hypothalamus consisted of mainly a ventricular germinal zone with a thin marginal layer, but by P25, most hypothalamic nuclei were well differentiated, indicating that the bulk of hypothalamic cytoarchitectural development occurs between P12 and P25. Strong CD 15 immunoreactivity was found in radial glial fibers in the rostral hypothalamus during early developmental ages, separating individual hypothalamic compartments. Immunoreactivity for GAP-43 was used to reveal developing fiber bundles. The medial forebrain bundle was apparent by P0, and the fornix appeared at P12. Tritiated thymidine autoradiography revealed lateral-to-medial and dorsal-to-ventral neurogenetic gradients similar to those seen in rodents. Dye tracing showed that projections to the posterior pituitary arose from the supraoptic nucleus at P5 and from the paraventricular nucleus at P10. Projections to the medulla were first found from the lateral hypothalamic area at P0 and paraventricular nucleus at P10. In conclusion, the pattern of development of the wallaby hypothalamus is broadly similar to that found in eutheria, with comparable neurogenetic compartments to those identified in rodents. Because most hypothalamic maturation takes place after birth, wallabies provide a useful model for experimentally manipulating the developing mammalian hypothalamus.
我们研究了澳大利亚有袋动物帚尾袋鼩(Macropus eugenii)下丘脑的发育情况,为今后对双门齿目有袋类动物发育中的下丘脑进行研究提供初步的解剖学框架。应用了细胞构筑学(苏木精和伊红染色)、免疫组织化学(CD15和生长相关蛋白GAP-43)、氚标记胸腺嘧啶核苷放射自显影术以及碳青霉烯染料示踪技术。出生后12天(P12)之前,发育中的下丘脑主要由一个带有薄边缘层的脑室生发区组成,但到P25时,大多数下丘脑核已充分分化,这表明下丘脑细胞构筑的大部分发育发生在P12和P25之间。在发育早期,在下丘脑前部的放射状胶质纤维中发现了强烈的CD15免疫反应性,将各个下丘脑隔室分开。GAP-43的免疫反应性用于揭示发育中的纤维束。内侧前脑束在P0时明显可见,穹窿在P12时出现。氚标记胸腺嘧啶核苷放射自显影术显示出与啮齿动物相似的从外侧到内侧以及从背侧到腹侧的神经发生梯度。染料示踪表明,向垂体后叶的投射在P5时起源于视上核,在P10时起源于室旁核。向延髓的投射最早在P0时从下丘脑外侧区发现,在P10时从室旁核发现。总之,帚尾袋鼩下丘脑的发育模式与真兽类动物的大致相似,具有与啮齿动物中确定的类似神经发生隔室。由于大多数下丘脑成熟发生在出生后,帚尾袋鼩为实验性操纵发育中的哺乳动物下丘脑提供了一个有用的模型。