Milaire J
Université Libre de Bruxelles, Faculty of Medicine, Department of Human Anatomy and Embryology, Belgium.
Anat Embryol (Berl). 1991;184(5):479-88. doi: 10.1007/BF01236054.
The binding sites of the following biotinylated lectins were demonstrated in serial paraffin sections of fore- and hindlimb buds from day-9 to day-16 mouse embryos with the Avidin-Biotin-Peroxidase Complex (ABC) procedure: Concanavalin A (Con A), Soybean Agglutinin (SBA), Wheat Germ Agglutinin (WGA), Peanut Agglutinin (PNA), Ricinus Communis Agglutinin I (RCA), Ulex Europaeus I Agglutinin (UEA), and Dolichos Biflorus Agglutinin (DBA). Alternating neighbouring sections were used to compare the distribution of PNA staining, PNA staining after neuraminidase treatment (N-PNA) and the autoradiographic sites of [35S]-sulphate uptake. Unspecific binding sites common to all lectins tested were observed in periderm and chondrocytes. Several lectin affinities were seen in the undifferentiated mesoderm (Con A, WGA, RCA), blood vessels (WGA, PNA, N-PNA, RCA, UEA, DBA) and macrophages (Con A, WGA, N-PNA, RCA). A very selective and mainly extracellular affinity to N-PNA was demonstrated in the condensed preskeletal mesoderm, where it characterizes indistinct prospective chondrogenic, perichondral and pre-articular areas. Comparison with the distribution pattern of [35S]-sulphate uptake and other previously published histochemical data suggests that N-PNA staining occurs at the late blastema stage, i.e. after the stage of cell condensation and before the earliest deposit of stainable matrix in chondrogenic areas. This property later disappears from the chondrifying rudiments, and is maintained in perichondral and pre-articular tissues. Surprisingly, only the pre-articular areas bind PNA without pretreatment with neuraminidase. A transient RCA binding probably related to terminal morphogenesis was detected in the undifferentiated distal part of the predigital columns of day-12 and day-13 limb buds. From the day-13 stage onwards, diverse new lectin affinities appeared in differentiating tissues, such as pretendinous rudiments, perichondrium and prospective periosteum, muscular connective tissue, myotubes, superficial fasciae and prospective dermis. A strong SBA and PNA staining was also detected in the extracellular matrix associated with the epithelial septa separating the roots of the digits in day-15 and day-16 limb buds.
采用抗生物素蛋白-生物素-过氧化物酶复合物(ABC)法,在第9天至第16天小鼠胚胎的前肢和后肢芽连续石蜡切片中,展示了以下生物素化凝集素的结合位点:刀豆球蛋白A(Con A)、大豆凝集素(SBA)、麦胚凝集素(WGA)、花生凝集素(PNA)、蓖麻凝集素I(RCA)、荆豆凝集素I(UEA)和双花扁豆凝集素(DBA)。使用相邻的交替切片来比较PNA染色、神经氨酸酶处理后的PNA染色(N-PNA)以及[35S] - 硫酸盐摄取的放射自显影位点分布情况。在周皮和软骨细胞中观察到所有测试凝集素共有的非特异性结合位点。在未分化中胚层(Con A、WGA、RCA)、血管(WGA、PNA、N-PNA、RCA、UEA、DBA)和巨噬细胞(Con A、WGA、N-PNA、RCA)中可见几种凝集素亲和力。在致密的前骨骼中胚层中显示出对N-PNA具有非常选择性且主要是细胞外的亲和力,在此处它表征不明确的潜在软骨形成、软骨膜和关节前区域。与[35S] - 硫酸盐摄取的分布模式及其他先前发表的组织化学数据比较表明,N-PNA染色出现在晚期芽基阶段,即在细胞凝聚阶段之后且在软骨形成区域最早可染色基质沉积之前。这种特性随后从软骨化原基中消失,并在软骨膜和关节前组织中保留。令人惊讶的是,只有关节前区域在未经神经氨酸酶预处理的情况下结合PNA。在第12天和第13天肢体芽的指前柱未分化远端部分检测到可能与终末形态发生相关的短暂RCA结合。从第13天阶段起,在分化组织中出现了多种新的凝集素亲和力,如假腱原基、软骨膜和潜在骨膜、肌肉结缔组织、肌管、浅筋膜和潜在真皮。在第15天和第16天肢体芽中,与分隔指根的上皮隔相关的细胞外基质中也检测到强烈的SBA和PNA染色。