Center for Fundamental Immunology, Matrix Biology Program, Benaroya Research Institute at Virginia Mason, Seattle, Washington.
J Histochem Cytochem. 2021 Jun;69(6):415-428. doi: 10.1369/00221554211022703.
Although many studies have focused on a role for hyaluronan (HA) of interstitial extracellular matrix (presumably produced by non-vascular "stromal" cells) in regulating vascular growth, we herein examine the influence of "autocrine HA" produced by vascular endothelial cells themselves on tubulogenesis, using human umbilical vein endothelial cells (HUVECs) in angiogenic and vasculogenic three-dimensional collagen gel cultures. Relative to unstimulated controls, tubulogenic HUVECs upregulated HAS2 mRNA and increased the synthesis of cell-associated HA (but not HA secreted into media). Confocal microscopy/immunofluorescence on cultures fixed with neutral-buffered 10% formalin (NBF) revealed cytoplasmic HAS2 in HUVEC cords and tubes. Cultures fixed with NBF (with cetylpyridinium chloride added to retain HA), stained for HA using "affinity fluorescence" (biotinylated HA-binding protein with streptavidin-fluor), and viewed by confocal microscopy showed HA throughout tube lumens, but little/no HA on the abluminal sides of the tubes or in the surrounding collagen gel. Lumen formation in angiogenic and vasculogenic cultures was strongly suppressed by metabolic inhibitors of HA synthesis (mannose and 4-methylumbelliferone). Hyaluronidase strongly inhibited lumen formation in angiogenic cultures, but not in vasculogenic cultures (where developing lumens are not open to culture medium). Collectively, our results point to a role for autocrine, luminal HA in microvascular sprouting and lumen development. .
虽然许多研究都集中在细胞外间质(推测由非血管“基质”细胞产生的)中的透明质酸(HA)在调节血管生长中的作用,但我们在此通过血管内皮细胞自身产生的“自分泌 HA”来研究其对血管生成和血管发生三维胶原凝胶培养中的小管形成的影响。与未刺激的对照相比,小管形成的 HUVEC 上调 HAS2 mRNA,并增加细胞相关 HA 的合成(但不包括分泌到培养基中的 HA)。用中性缓冲 10%甲醛(NBF)固定的培养物的共聚焦显微镜/免疫荧光显示 HUVEC 索和管中的细胞质 HAS2。用 NBF(加入十六烷基吡啶氯以保留 HA)固定的培养物,使用“亲和荧光”(带有链霉亲和素的生物素化 HA 结合蛋白)对 HA 进行染色,并通过共聚焦显微镜观察,显示 HA 遍布管腔,但管腔的基底侧或周围的胶原凝胶中 HA 较少/无。血管生成和血管发生培养物中的管腔形成强烈受到 HA 合成代谢抑制剂(甘露糖和 4-甲基伞形酮)的抑制。透明质酸酶强烈抑制血管生成培养物中的管腔形成,但不抑制血管发生培养物(其中正在发育的管腔未向培养基开放)。总之,我们的结果表明,自分泌的管腔 HA 在微血管发芽和管腔发育中起作用。