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Adaptable haemodynamic endothelial cells for organogenesis and tumorigenesis.

Nature | 2020

Endothelial cells adopt tissue-specific characteristics to instruct organ development and regeneration1,2. This adaptability is lost in cultured adult endothelial cells, which do not vascularize tissues in an organotypic manner. Here, we show that transient reactivation of the embryonic-restricted ETS variant transcription factor 2 (ETV2)3 in mature human endothelial cells cultured in a serum-free three-dimensional matrix composed of a mixture of laminin, entactin and type-IV collagen (LEC matrix) 'resets' these endothelial cells to adaptable, vasculogenic cells, which form perfusable and plastic vascular plexi. Through chromatin remodelling, ETV2 induces tubulogenic pathways, including the activation of RAP1, which promotes the formation of durable lumens4,5. In three-dimensional matrices-which do not have the constraints of bioprinted scaffolds-the 'reset' vascular endothelial cells (R-VECs) self-assemble into stable, multilayered and branching vascular networks within scalable microfluidic chambers, which are capable of transporting human blood. In vivo, R-VECs implanted subcutaneously in mice self-organize into durable pericyte-coated vessels that functionally anastomose to the host circulation and exhibit long-lasting patterning, with no evidence of malformations or angiomas. R-VECs directly interact with cells within three-dimensional co-cultured organoids, removing the need for the restrictive synthetic semipermeable membranes that are required for organ-on-chip systems, therefore providing a physiological platform for vascularization, which we call 'Organ-On-VascularNet'. R-VECs enable perfusion of glucose-responsive insulin-secreting human pancreatic islets, vascularize decellularized rat intestines and arborize healthy or cancerous human colon organoids. Using single-cell RNA sequencing and epigenetic profiling, we demonstrate that R-VECs establish an adaptive vascular niche that differentially adjusts and conforms to organoids and tumoroids in a tissue-specific manner. Our Organ-On-VascularNet model will permit metabolic, immunological and physiochemical studies and screens to decipher the crosstalk between organotypic endothelial cells and parenchymal cells for identification of determinants of endothelial cell heterogeneity, and could lead to advances in therapeutic organ repair and tumour targeting.

Pubmed ID: 32908310 RIS Download

Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: DP3 DK111907
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL119215
  • Agency: NIH HHS, United States
    Id: 1R21AI117213
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL115128
  • Agency: NIA NIH HHS, United States
    Id: R01 AG056298
  • Agency: NHLBI NIH HHS, United States
    Id: R35 HL150809
  • Agency: NIAID NIH HHS, United States
    Id: R21 AI117213
  • Agency: NIMH NIH HHS, United States
    Id: F30 MH115616
  • Agency: NIDDK NIH HHS, United States
    Id: R03 DK117252
  • Agency: NIDDK NIH HHS, United States
    Id: UC4 DK116280
  • Agency: NIAAA NIH HHS, United States
    Id: R01 AA027327
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL119872
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK106253
  • Agency: NIDDK NIH HHS, United States
    Id: P30 DK089503
  • Agency: NCI NIH HHS, United States
    Id: R01 CA194547
  • Agency: NCI NIH HHS, United States
    Id: R01 CA234614
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL128158
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK095039
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR002384
  • Agency: Medical Research Council, United Kingdom
    Id: MR/N028414/1
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK121072
  • Agency: NIDDK NIH HHS, United States
    Id: RC2 DK114777
  • Agency: NIDDK NIH HHS, United States
    Id: K08 DK101754
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL139056
  • Agency: NIAID NIH HHS, United States
    Id: R01 AI107301
  • Agency: NIAID NIH HHS, United States
    Id: U01 AI138329

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