Department of Signal Transduction, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
J Thromb Haemost. 2011 Jul;9 Suppl 1:144-50. doi: 10.1111/j.1538-7836.2011.04275.x.
While blood vessels clearly have a fundamental role in supplying oxygen and nutrients, and transporting inflammatory cells throughout the body, they are also involved in organogenesis and maintenance. Blood vessels provide a niche that supports self-renewal of stem cell populations in normal organs. This role unfortunately also extends to the field of cancer biology; it has been suggested that cancer stem cells are located in perivascular regions supporting their proliferation. Through cell-to-cell interactions, arteries also have the important function of guiding appropriate migration of neurites. Therefore, analysis of the molecular mechanisms responsible for blood vessel formation and maintenance is important for developing strategies to regulate tissue regeneration. According to the usual concept of angiogenesis, it is widely accepted that homogeneous endothelial cells from preexisting vessels sprout and proliferate during angiogenesis. Recently, however, at least three different endothelial cell types designated tip, stalk and phalanx cells have been suggested to be involved in new blood vessel formation in sprouting angiogenesis. Given this endothelial cell heterogeneity, the involvement of a stem cell system in preexisting blood vessels is proposed. In addition, endothelial cells possess the capacity to differentiate into mesenchymal stem cells upon stimulation with growth factors, and pericytes show stem cell behaviour in their ability to differentiate into a variety of different histotypes. Moreover, under normal physiological conditions, haematopoietic stem cells differentiate into mural cells to provide blood vessel stability. These findings make it necessary to reconsider issues concerning the regulation of blood vessels by accessory cells situated around those vessels.
虽然血管在为全身供应氧气和营养物质以及输送炎症细胞方面具有重要作用,但它们也参与器官发生和维持。血管提供了一个龛位,支持正常器官中干细胞群体的自我更新。不幸的是,这个角色也扩展到了癌症生物学领域;有人提出,癌症干细胞位于支持其增殖的血管周围区域。通过细胞间的相互作用,动脉还有一个重要的功能,即引导神经元突的适当迁移。因此,分析负责血管形成和维持的分子机制对于制定调节组织再生的策略非常重要。根据血管生成的通常概念,广泛接受的观点是,同质的内皮细胞从前存在的血管中发芽和增殖,从而参与血管生成。然而,最近,至少有三种不同的内皮细胞类型(指定为尖端、干和指状细胞)被认为参与了发芽血管生成中的新血管形成。鉴于这种内皮细胞异质性,提出了前存在血管中存在干细胞系统的参与。此外,内皮细胞在受到生长因子刺激时具有分化为间充质干细胞的能力,而周细胞在分化为多种不同组织型的能力上表现出干细胞行为。此外,在正常生理条件下,造血干细胞分化为壁细胞以提供血管稳定性。这些发现使得有必要重新考虑与位于这些血管周围的辅助细胞调节血管有关的问题。