Epperlein Hans Henning, Claviez Michael
Abt. Physikal. Biologie, Max-Planck-Institut für Virusforschung, Spemannstrasse 35, 74 Tübingen, Federal Republic of Germany.
Wilehm Roux Arch Dev Biol. 1982 Jan;191(1):5-18. doi: 10.1007/BF00848541.
The change in distribution of melanophores from stage 28+ (uniform melanophore pattern) to stage 34 (banded melanophore pattern) and the participation of xanthophores in these changes has been investigated inTriturus alpestris embryos by studying the social behaviour of single cells. While melanophores are clearly visible from outside the embryo at stage 28+, xanthophores cannot be recognized from the outside until after stage 34. In ultrathin sections of stage 34 embryos, xanthophores are observed alternating with melanophores in a zonal distribution (Epperlein 1982). Using detached pieces of dorsolateral trunk skin, which retain their chromatophores after detachment, the entire distribution of melanophores and xanthophores can be visualized in a scanning electron microscope (SEM). In ambiguous cases (early stages), cells were reprocessed for transmission electron microscopy (TEM) and the presence of the characteristic pigment organelles was assessed. In addition, xanthophores were specifically identified by pteridine fluorescence with dilute ammonia. Pteridines were also identified chromatographically in skin homogenates. The combination of these methods allowed precise identification and quantitative determination of melanophores and xanthophores. Both cell types were present as codistributed, biochemically differentiated cells at stage 28+. Changes in the pattern up to stage 34 were due to the rearrangement at the epidermal-mesodermal interface of a relatively fixed number of melanophores which became preferentially localised at the dorsal somite edge and at the lateral plate mesoderm, and to the distribution of an increasing number of xanthophores to subepidermal locations in the dorsal fin and between the melanophore bands. Concomitant was an increase in the thickness of the epidermal basement membrane and a change in shape of chromatophores from elongate via stellate to rosette shaped, which may be correlated with a shift from migratory to sessile phases.
通过研究单细胞的社会行为,对高山蝾螈胚胎中从28 +期(均匀黑素细胞模式)到34期(带状黑素细胞模式)黑素细胞分布的变化以及黄色素细胞在这些变化中的参与情况进行了研究。在28 +期,黑素细胞从胚胎外部清晰可见,而黄色素细胞直到34期后才能从外部识别出来。在34期胚胎的超薄切片中,观察到黄色素细胞与黑素细胞呈带状交替分布(埃佩尔莱茵,1982)。使用背外侧躯干皮肤的分离片段,其在分离后仍保留色素细胞,黑素细胞和黄色素细胞的整体分布可在扫描电子显微镜(SEM)中可视化。在不明确的情况下(早期阶段),将细胞重新处理用于透射电子显微镜(TEM)检查,并评估特征性色素细胞器的存在情况。此外,通过用稀氨进行蝶啶荧光特异性鉴定黄色素细胞。还通过色谱法在皮肤匀浆中鉴定蝶啶。这些方法的结合使得能够精确鉴定和定量测定黑素细胞和黄色素细胞。在28 +期,两种细胞类型作为共分布、生化分化的细胞存在。直至34期模式的变化是由于相对固定数量的黑素细胞在表皮 - 中胚层界面重新排列,这些黑素细胞优先定位在背侧体节边缘和侧板中胚层,以及越来越多的黄色素细胞分布到背鳍的表皮下位置和黑素细胞带之间。同时,表皮基底膜厚度增加,色素细胞形状从细长形经星状变为玫瑰花结形,这可能与从迁移阶段到固定阶段的转变相关。