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爬行动物、鸟类和哺乳动物的真皮-表皮重组中皮肤附属器的形成。

Formation of cutaneous appendages in dermo-epidermal recombinations between reptiles, birds and mammals.

作者信息

Dhouailly Danielle

机构信息

Laboratoire de Zoologie de l'Université Scientifique et Médicale de Grenoble, Boîte Postale 53, 38041, Grenoble, France.

出版信息

Wilehm Roux Arch Dev Biol. 1975 Dec;177(4):323-340. doi: 10.1007/BF00848183.


DOI:10.1007/BF00848183
PMID:28305000
Abstract
  1. Previous experiments on dermo-epidermal recombinations between birds and mammals have shown that the class-specific quality of the cutaneous appendages depends on intrinsic properties of the epidermis but that several steps of their morphogenesis are controlled by the dermis. This morphogenetic interplay has been tested further in new experiments with reptilian skin. 2. Reconstituted homo- and heterospecific skin explants, involving epidermis and dermis of lizard, chick and mouse, were cultured for 8 days on the chorioallantoic membrane of the chick embryo. 3. Homospecific recombinations of dorsal, caudal or ventral lizard epidermis and dorsal lizard dermis gave rise to small dorsal-type scales. Recombinants of dorsal, caudal or ventral lizard epidermis and ventral lizard dermis gave rise to large ventral-type scales. 4. Heterospecific recombinations of dorsal, caudal or ventral lizard epidermis and chick dermis from the glabrous comb region did not differentiate any scale structures. 5. Heterospecific recombinations of dorsal or caudal lizard epidermis and tarsometatarsal chick dermis formed large chick-type scales. 6. Heterospecific recombinations of dorsal, caudal or ventral lizard epidermis and chick feather-forming, or mouse hair-forming or whisker-forming dermis gave rise to tubercular scale primordia. The diameter and distribution of these primordia were in conformity with the feather, pelage hair and vibrissal patterns respectively. 7. Heterospecific association of lizard dermis and chick or mouse epidermis led to the formation of few epidermal placode-like pegs; those differentiated by the mouse epidermis were interpreted as hair bud structures. 8. The differentiation of reptilian scales is the result of dermo-epidermal interactions. Reptilian epidermis, when confronted with either reptilian, avian, or mammalian dermis, always responds to the dermal messages by forming scale buds. For final scale morphogenesis, however, reptilian dermis or avian scale-forming dermis is required. Reptilian dermis appears to be unable to induce extensive appendage formation in avian or mammalian epidermis. 9. A remarkable similarity exists in the mechanisms of skin differentiation in the three classes of amniotes. Indeed scales, feathers and hairs require two kinds of dermal messages for their complete morphogenesis: early ones, which can be transmitted from one class to another, and which are responsible for the initiation, site, size and distribution pattern of appendage primordia, whose class-specific quality (scale, feather or hair buds) is determined by the epidermis; and later specific ones which can only be understood within the class and which are necessary for the completion of the specific architecture of the cutaneous appendage.
摘要
  1. 先前关于鸟类和哺乳动物之间皮肤-表皮重组的实验表明,皮肤附属器的类别特异性特征取决于表皮的内在特性,但其形态发生的几个步骤受真皮控制。这种形态发生的相互作用在涉及爬行动物皮肤的新实验中得到了进一步验证。2. 将含有蜥蜴、鸡和小鼠的表皮与真皮的同种和异种特异性皮肤外植体在鸡胚的尿囊膜上培养8天。3. 蜥蜴背部、尾部或腹部表皮与蜥蜴背部真皮的同种特异性重组产生了小的背部型鳞片。蜥蜴背部、尾部或腹部表皮与蜥蜴腹部真皮的重组产生了大的腹部型鳞片。4. 蜥蜴背部、尾部或腹部表皮与来自无毛鸡冠区域的鸡真皮的异种特异性重组未分化出任何鳞片结构。5. 蜥蜴背部或尾部表皮与跗跖部鸡真皮的异种特异性重组形成了大的鸡型鳞片。6. 蜥蜴背部、尾部或腹部表皮与鸡羽毛形成区、或小鼠毛发生成区或触须形成区真皮的异种特异性重组产生了结节状鳞片原基。这些原基的直径和分布分别与羽毛、被毛和触须的模式一致。7. 蜥蜴真皮与鸡或小鼠表皮的异种结合导致形成少数表皮基板样凸起;由小鼠表皮分化形成的那些被解释为毛芽结构。8. 爬行动物鳞片的分化是皮肤-表皮相互作用的结果。当爬行动物表皮与爬行动物、鸟类或哺乳动物真皮接触时,总是通过形成鳞片芽对真皮信号作出反应。然而,对于最终的鳞片形态发生,需要爬行动物真皮或鸟类鳞片形成区真皮。爬行动物真皮似乎无法在鸟类或哺乳动物表皮中诱导广泛的附属器形成。9. 三类羊膜动物的皮肤分化机制存在显著相似性。事实上,鳞片、羽毛和毛发的完全形态发生需要两种真皮信号:早期信号,可从一类传递到另一类,负责附属器原基的起始、位置、大小和分布模式,其类别特异性特征(鳞片、羽毛或毛芽)由表皮决定;以及后期特定信号,只能在同一类中理解,是皮肤附属器特定结构完成所必需的。

相似文献

[1]
Formation of cutaneous appendages in dermo-epidermal recombinations between reptiles, birds and mammals.

Wilehm Roux Arch Dev Biol. 1975-12

[2]
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[3]
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