Computational simulations of the 4D micro-circulatory network in zebrafish tail amputation and regeneration

Author:

Roustaei Mehrdad12ORCID,In Baek Kyung12,Wang Zhaoqiang12,Cavallero Susana2,Satta Sandro2,Lai Angela2,O'Donnell Ryan2ORCID,Vedula Vijay3,Ding Yichen4,Marsden Alison Lesley5,Hsiai Tzung K.126

Affiliation:

1. Department of Bioengineering, University of California Los Angeles, Los Angeles, CA, USA

2. Division of Cardiology, Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA

3. Department of Mechanical Engineering, Columbia University, New York, NY, USA

4. Department of Bioengineering, University of Texas Dallas, Dallas, TX, USA

5. Department of Pediatrics and Bioengineering, Stanford University, Stanford, CA, USA

6. Division of Cardiology, Department of Medicine, Greater Los Angeles VA Healthcare System, Los Angeles, CA, USA

Abstract

Wall shear stress (WSS) contributes to the mechanotransduction underlying microvascular development and regeneration. Using computational fluid dynamics, we elucidated the interplay between WSS and vascular remodelling in a zebrafish model of tail amputation and regeneration. The transgenic Tg ( fli1:eGFP ; Gata1:ds-red ) zebrafish line was used to track the three-dimensional fluorescently labelled vascular endothelium for post-image segmentation and reconstruction of the fluid domain. Particle image velocimetry was used to validate the blood flow. Following amputation to the dorsal aorta and posterior cardinal vein (PCV), vasoconstriction developed in the dorsal longitudinal anastomotic vessel (DLAV) along with increased WSS in the proximal segmental vessels (SVs) from amputation. Angiogenesis ensued at the tips of the amputated DLAV and PCV where WSS was minimal. At 2 days post amputation (dpa), vasodilation occurred in a pair of SVs proximal to amputation, followed by increased blood flow and WSS; however, in the SVs distal to amputation, WSS normalized to the baseline. At 3 dpa, the blood flow increased in the arterial SV proximal to amputation and through anastomosis with DLAV formed a loop with PCV. Thus, our in silico modelling revealed the interplay between WSS and microvascular adaptation to changes in WSS and blood flow to restore microcirculation following tail amputation.

Funder

National Institutes of Health

Publisher

The Royal Society

Subject

Biomedical Engineering,Biochemistry,Biomaterials,Bioengineering,Biophysics,Biotechnology

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