Abstract

Angiogenesis is a process through which new blood vessels are formed by sprouting and elongating from existing blood vessels. Several methods have been used to replicate angiogenesis in vitro, including culturing vascular endothelial cells on Matrigel and coculturing with endothelial cells and fibroblasts. However, the angiogenesis elongation process has not been completely clarified in these models. We therefore propose a new in vitro model of angiogenesis, suitable for observing vascular elongation, by seeding a spheroid cocultured from endothelial cells and fibroblasts into a culture dish. In this model, endothelial cells formed tubular networks elongated from the spheroid with a lumen structure and were connected with tight junctions. A basement membrane (BM)-like structure was observed around the tubular network, similarly to blood vessels in vivo. These results suggested that blood vessel-like structure could be reconstituted in our model. Laminin and type IV collagen, main BM components, were highly localized around the network, along with nontriple helical form of type IV collagen α1-chain [NTH α1(IV)]. In an ascorbic acid-depleted condition, laminin and NTH α1(IV) were observed around the network but not the triple-helical form of type IV collagen and the network was unstable. These results suggest that laminin and NTH α1(IV) are involved in the formation of tubular network and type IV collagen is necessary to stabilize the network.

Highlights

  • Angiogenesis is a process of new blood vessel formation from preexisting vasculature

  • In TIG-1, laminins were localized to a spot (Fig. 7C). These results suggest that triple-helical type IV collagen is not necessary for the formation of Human umbilical vein endothelial cells (HUVECs) tubular structures and interaction of HUVECs with TIG-1 induces NTH ␣1(IV) to localize along the network, even in the presence of ascorbic acid (AA)

  • We investigated a novel angiogenesis model, 2.5D coculture system in which HUVEC and TIG-1 formed 3D spheroids and were seeded onto culture dishes or cover glasses (2.5D), where sprouting and elongating endothelial cells (ECs) tubular networks could be observed

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Summary

Introduction

Angiogenesis is a process of new blood vessel formation from preexisting vasculature. It plays important roles in several physiological or pathophysiological processes such as wound healing, female reproductive cycles, and tumor growth and metastasis [6]. The nontriple helical type IV collagen ␣1 [NTH ␣1(IV)] chain is secreted from human fetal lung fibroblasts (TIG-1), mesangial cells, or ECs in the absence of AA [42, 45]. In the neovascular tip region of ECs, NTH ␣1(IV) has been exclusively observed; triple- helical type IV collagen has not been detected [41]. NTH ␣1(IV) may play a physiological role in angiogenesis

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