Carvalhaes Lorenza S, Gervásio Othon L, Guatimosim Cristina, Heljasvaara Ritva, Sormunen Raija, Pihlajaniemi Taina, Kitten Gregory T
Department of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Dev Dyn. 2006 Jan;235(1):132-42. doi: 10.1002/dvdy.20556.
Type XVIII collagen is a multidomain protein that contains cleavable C-terminal NC1 and endostatin fragments, which have been shown to either induce or inhibit cell migration. Endostatin is being intensely studied because of its anti-angiogenic activity. Three variants of type XVIII collagen have been reported to be distributed in epithelial and endothelial basement membranes in a tissue-specific manner. The single gene encoding collagen XVIII is on chromosome 21 within the region associated with the congenital heart disease phenotype observed in Down's syndrome. In this study, we investigated the expression pattern of collagen XVIII in embryonic mouse hearts during formation of the atrioventricular (AV) valves. We found that collagen XVIII is localized not only in various basement membranes but is also highly expressed throughout the connective tissue core of the endocardial cushions and forming AV valve leaflets. It was closely associated with the epithelial-mesenchymal transformation of endothelial cells into mesenchymal cushion tissue cells and was localized around these cells as they migrated into the cardiac jelly to form the initial connective tissue elements of the valve leaflets. However, after embryonic day 17.5 collagen XVIII expression decreased rapidly in the connective tissue and thereafter remained detectable only in the basement membranes of the endothelial layer covering the leaflets. The staining pattern observed within the AV endocardial cushions suggests that collagen XVIII may have a role in cardiac valve morphogenesis. These results may help us to better understand normal heart development and the aberrant mechanisms that cause cardiac malformations in Down's syndrome.
ⅩⅧ型胶原蛋白是一种多结构域蛋白,包含可裂解的C末端NC1和内皮抑素片段,这些片段已被证明可诱导或抑制细胞迁移。由于其抗血管生成活性,内皮抑素正在被深入研究。据报道,ⅩⅧ型胶原蛋白的三种变体以组织特异性方式分布在上皮和内皮基底膜中。编码胶原蛋白ⅩⅧ的单基因位于21号染色体上与唐氏综合征中观察到的先天性心脏病表型相关的区域内。在本研究中,我们调查了胚胎小鼠心脏在房室(AV)瓣膜形成过程中ⅩⅧ型胶原蛋白的表达模式。我们发现,ⅩⅧ型胶原蛋白不仅定位于各种基底膜中,而且在心内膜垫的结缔组织核心和正在形成的AV瓣膜小叶中也高度表达。它与内皮细胞向间充质垫组织细胞的上皮-间充质转化密切相关,并在这些细胞迁移到心胶中形成瓣膜小叶的初始结缔组织成分时定位于它们周围。然而,在胚胎第17.5天之后,ⅩⅧ型胶原蛋白在结缔组织中的表达迅速下降,此后仅在覆盖小叶的内皮细胞层的基底膜中仍可检测到。在AV心内膜垫中观察到的染色模式表明,ⅩⅧ型胶原蛋白可能在心脏瓣膜形态发生中起作用。这些结果可能有助于我们更好地理解正常心脏发育以及导致唐氏综合征心脏畸形的异常机制。