Simon-Assmann P, Bouziges F, Vigny M, Kedinger M
Institut National de la Santé et de la Recherche Medicale, Unité 61, Biologie Cellulaire et Physiopathologie Digestives, Strasbourg, France.
J Cell Biol. 1989 Oct;109(4 Pt 1):1837-48. doi: 10.1083/jcb.109.4.1837.
The deposition of intestinal heparan sulfate proteoglycan (HSPG) at the epithelial-mesenchymal interface and its cellular source have been studied by immunocytochemistry at various developmental stages and in rat/chick interspecies hybrid intestines. Polyclonal heparan sulfate antibodies were produced by immunizing rabbits with HSPG purified from the Engelbreth-Holm-Swarm mouse tumor; these antibodies stained rat intestinal basement membranes. A monoclonal antibody (mAb 4C1) produced against lens capsule of 11-d-old chick embryo reacted with embryonic or adult chick basement membranes, but did not stain that of rat tissues. Immunoprecipitation experiments indicated that mAb 4C1 recognized the chicken basement membrane HSPG. Immunofluorescent staining with these antibodies allowed us to demonstrate that distribution of HSPG at the epithelial-mesenchymal interface varied with the stages of intestinal development, suggesting that remodeling of this proteoglycan is essential for regulating cell behavior during morphogenesis. The immunofluorescence pattern obtained with the two species-specific HSPG antibodies in rat/chick epithelial/mesenchymal hybrid intestines developed as grafts (into the coelomic cavity of chick embryos or under the kidney capsule of adult mice) led to the conclusion that HSPG molecules located in the basement membrane of the developing intestine were produced exclusively by the epithelial cells. These data emphasize the notion already gained from previous studies, in which type IV collagen has been shown to be produced by mesenchymal cells (Simon-Assmann, P., F. Bouziges, C. Arnold, K. Haffen, and M. Kedinger. 1988. Development (Camb.). 102:339-347), that epithelial-mesenchymal interactions play an important role in the formation of a complete basement membrane.
通过免疫细胞化学方法,在不同发育阶段以及大鼠/鸡种间杂交肠中,研究了肠道硫酸乙酰肝素蛋白聚糖(HSPG)在上皮-间充质界面的沉积及其细胞来源。用从恩格尔布雷特-霍尔姆-斯旺小鼠肿瘤中纯化的HSPG免疫兔子,制备多克隆硫酸乙酰肝素抗体;这些抗体可对大鼠肠基底膜进行染色。一种针对11日龄鸡胚晶状体囊产生的单克隆抗体(mAb 4C1)可与胚胎或成年鸡的基底膜发生反应,但不能对大鼠组织的基底膜进行染色。免疫沉淀实验表明,mAb 4C1识别鸡基底膜HSPG。用这些抗体进行免疫荧光染色,使我们能够证明HSPG在上皮-间充质界面的分布随肠道发育阶段而变化,这表明这种蛋白聚糖的重塑对于调节形态发生过程中的细胞行为至关重要。在作为移植物(植入鸡胚体腔或成年小鼠肾被膜下)发育的大鼠/鸡上皮/间充质杂交肠中,用两种物种特异性HSPG抗体获得的免疫荧光模式得出结论,即发育中肠道基底膜中的HSPG分子仅由上皮细胞产生。这些数据强调了先前研究中已经得出的观点,其中已表明IV型胶原由间充质细胞产生(Simon-Assmann, P., F. Bouziges, C. Arnold, K. Haffen, and M. Kedinger. 1988. Development (Camb.). 102:339 - 347),即上皮-间充质相互作用在完整基底膜的形成中起重要作用。