Peters J H, Chen G E, Hynes R O
Division of Pulmonary and Critical Care Medicine, Cedars-Sinai Medical Center, Los Angeles, California 90048, USA.
Cell Adhes Commun. 1996 Aug;4(2):127-48. doi: 10.3109/15419069609010767.
The alternatively spliced EIIIB, EIIIA, and V segments of fibronectin (FN) show widespread codistribution in the mouse embryo, suggesting that EIIIB+, EIIIA+, and V+ isoforms serve to facilitate morphogenesis and organogenesis (Peters, JH, and Hynes, RO, 1996, this issue). To gain further clues to functions of these segments, we have used segment-specific anti-FN antibodies to perform immunofluorescence microscopy on tissue sections obtained from mice aged 9 to 15 weeks. Staining for each of the three spliced segments, relative to that for the total FN pool, was reduced in the adult as compared with the embryo. Anti-V antibodies produced patterns which were most similar to those obtained with anti-total FN antibodies, localizing to basement membranes, connective tissues subjacent to epithelia, walls of blood vessels, and cartilage. Anti-EIIIA antibodies produced the next most widespread pattern, which included prominent staining of the walls of blood vessels of all sizes, the lung interstitium, and smooth muscle associated with the gastrointestinal (GI), genitourinary (GU), and respiratory tracts. Although anti-EIIIB antibodies produced the faintest and most restricted pattern of staining, EIIIB+ FN could be detected in the walls of some smaller blood vessels, smooth muscle of the GI, GU, and respiratory tracts, as well as within cartilaginous structures, and eye. There were quantitative and/or qualitative differences in the staining patterns produced by the three segment-specific antibodies in a variety of tissues, including liver, cartilage, synovium, cornea, muscle, peripheral nerve, and lymph node. These findings suggest that each of the spliced segments of the FN molecule may occupy unique physical or functional positions within the extracellular matrix of the adult mouse.
纤连蛋白(FN)的可变剪接EIIIB、EIIIA和V片段在小鼠胚胎中广泛共分布,这表明EIIIB +、EIIIA +和V +同工型有助于促进形态发生和器官发生(Peters,JH和Hynes,RO,1996年,本期)。为了进一步了解这些片段的功能,我们使用片段特异性抗FN抗体对9至15周龄小鼠的组织切片进行免疫荧光显微镜检查。与胚胎相比,成年小鼠中这三个剪接片段相对于总FN池的染色均减少。抗V抗体产生的模式与抗总FN抗体获得的模式最相似,定位于基底膜、上皮下方的结缔组织、血管壁和软骨。抗EIIIA抗体产生的模式次之,包括所有大小血管壁、肺间质以及与胃肠道(GI)、泌尿生殖道(GU)和呼吸道相关的平滑肌的明显染色。尽管抗EIIIB抗体产生的染色模式最淡且最局限,但在一些较小血管壁、GI、GU和呼吸道的平滑肌以及软骨结构和眼中可检测到EIIIB + FN。在包括肝脏、软骨、滑膜、角膜、肌肉、周围神经和淋巴结在内的多种组织中,三种片段特异性抗体产生的染色模式存在定量和/或定性差异。这些发现表明,FN分子的每个剪接片段在成年小鼠的细胞外基质中可能占据独特的物理或功能位置。