Tripathi B J, Tripathi R C, Livingston A M, Borisuth N S
Department of Ophthalmology and Visual Science, University of Chicago, Illinois.
Am J Anat. 1991 Dec;192(4):442-71. doi: 10.1002/aja.1001920411.
The vertebrate eye is composed of a variety of tissues that, embryonically, have their derivation from surface ectoderm, neural ectoderm, neural crest, and mesodermal mesenchyme. During development, these different types of cells are subjected to complex processes of induction and suppressive interactions that bring about their final differentiation and arrangement in the fully formed eye. With the changing concept of ocular development, we present a new perspective on the control of morphogenesis at the cellular and molecular levels by growth factors that include fibroblast growth factors, epidermal growth factor, nerve growth factor, platelet-derived growth factor, transforming growth factors, mesodermal growth factors, transferrin, tumor necrosis factor, neuronotrophic factors, angiogenic factors, and antiangiogenic factors. Growth factors, especially transforming growth factor-beta, have a crucial role in directing the migration and developmental patterns of the cranial neural-crest cells that contribute extensively to the structures of the eye. Some growth factors also exert an effect on the developing ocular tissues by influencing the synthesis and degradation of the extracellular matrix. The mRNAs for the growth factors that are involved in the earliest aspects of the growth and differentiation of the fertilized egg are supplied from maternal sources until embryonic tissues are able to synthesize them. Subsequently, the developing eye tissues are exposed to both endogenous and exogenous growth factors that are derived from nonocular tissues as well as from embryonic fluids and the systemic circulation. The early interaction between the surface head ectoderm and the underlying chordamesoderm confers a lens-forming bias on the ectoderm; later, the optic vesicle elicits the final phase of determination and enhances differentiation by the lens. After the blood-ocular barrier is established, the internal milieu of the eye is controlled by the interactions among the intraocular tissues; only those growth factors that selectively cross the barrier or that are synthesized by the ocular tissues can influence further development and differentiation of the cells. An understanding of the tissue interactions that are regulated by growth factors could clarify the precise mechanism of normal and abnormal ocular development.
脊椎动物的眼睛由多种组织构成,在胚胎发育过程中,这些组织来源于表面外胚层、神经外胚层、神经嵴和中胚层间充质。在发育过程中,这些不同类型的细胞会经历复杂的诱导和抑制相互作用过程,从而实现它们在完全形成的眼睛中的最终分化和排列。随着眼发育概念的不断变化,我们从细胞和分子水平上提出了一个关于生长因子对形态发生控制的新观点,这些生长因子包括成纤维细胞生长因子、表皮生长因子、神经生长因子、血小板衍生生长因子、转化生长因子、中胚层生长因子、转铁蛋白、肿瘤坏死因子、神经营养因子、血管生成因子和抗血管生成因子。生长因子,尤其是转化生长因子-β,在引导对眼睛结构有广泛贡献的颅神经嵴细胞的迁移和发育模式方面起着关键作用。一些生长因子还通过影响细胞外基质的合成和降解,对发育中的眼组织产生影响。参与受精卵生长和分化最早阶段的生长因子的mRNA由母体提供,直到胚胎组织能够合成它们。随后,发育中的眼组织会接触到来自非眼组织以及胚胎液和体循环的内源性和外源性生长因子。表面头部外胚层与下方脊索中胚层之间的早期相互作用赋予外胚层形成晶状体的倾向;后来,视泡引发决定的最后阶段,并增强晶状体的分化。血眼屏障建立后,眼的内部环境由眼内组织之间的相互作用控制;只有那些选择性穿过屏障或由眼组织合成的生长因子才能影响细胞的进一步发育和分化。了解由生长因子调节的组织相互作用可以阐明正常和异常眼发育的精确机制。