A biologic process that rapidly expands vascular networks is intussusceptive (nonsprouting) angiogenesis. Vascular expansion occurs by the active subdivision of one vessel into two lumens. The earliest stage of this process is characterized by the formation of tissue islands or intraluminal """"""""pillars."""""""" We have found these intravascular pillars in the skin (dermatitis), colon (colitis) and lung (post-pneumonectomy). Growth or extension of the intraluminal pillars down the axis of the vessel leads to vessel duplication. The rate of pillar extension and vascular division appears to far exceed the proliferative capacity of resident endothelial cells. This project addresses the following question How is the process of adult intussusceptive angiogenesis capable of such rapid blood vessel expansion;further, how can this process be harnessed for therapeutic angiogenesis? To answer this question, we have developed a parabiotic mouse model of post-pneumonectomy intussusceptive angiogenesis. In the parabiotic model, wild-type and green fluorescence protein (GFP) mice are surgically paired to establish complete cross-circulation. After establishing a shared circulation, a pneumonectomy is performed in the wild-type mouse. Morphometry demonstrates that the remaining lung develops 1-3 kilometers of new alveolar capillaries within 2 weeks of pneumonectomy. Corrosion casting and 3-dimensional scanning electron microscopy shows that this blood vessel growth is largely produced by intense intussusceptive angiogenesis. An important clue to understanding the process of intussusceptive angiogenesis is the observation that post-pneumonectomy vessel growth is associated with GFP+ endothelial cells. Since the intussusceptive angiogenesis occurs in the wild-type mouse, GFP+ cells in the vascular lining must be derived from the peripheral blood circulation. These GFP+ endothelial progenitor cells (EPC) not only demonstrate the importance of EPC in intussusceptive angiogenesis, but they provide an explanation for the rapid rate of vascular expansion. Adding further support for the importance of EPC, we have demonstrated that, in studies of parabiotic colitis, blood-borne EPC localize near intussusceptive pillars. To test our hypothesis that intussusceptive pillars localize circulating EPC, we will use the parabiotic model to track endothelial progenitor cells (EPC) from their mobilization in the bone marrow to their migration into the lung during parabiotic post-pneumonectomy intussusceptive angiogenesis (Specific Aim #1). Advanced imaging will determine the effect of intussusceptive pillars on EPC localization, vascular integration and total angiogenesis (Specific Aim #2). Finally, the intravascular interaction of EPC and pillars during intussusceptive angiogenesis will be modeled in vitro and in silico (Specific Aim #3). The goal of this project is the functional regulation of adult intussusceptive angiogenesis;that is, the rapid expansion of microvascular networks for application in both regenerative medicine and tissue engineering.

Public Health Relevance

This project investigates the control of a adaptive physiologic process capable of triggering the growth and regeneration of blood vessels. The ultimate goal is to harness these adaptive forces for the therapeutic control of human tissue growth and repair.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL094567-06
Application #
8690133
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Gao, Yunling
Project Start
2008-12-01
Project End
2017-05-31
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
6
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02115
Servais, Andrew B; Kienzle, Arne; Ysasi, Alexandra B et al. (2018) Structural heteropolysaccharides as air-tight sealants of the human pleura. J Biomed Mater Res B Appl Biomater :
Kienzle, Arne; Servais, Andrew B; Ysasi, Alexandra B et al. (2018) Free-Floating Mesothelial Cells in Pleural Fluid After Lung Surgery. Front Med (Lausanne) 5:89
Haber, Shimon; Weisbord, Michal; Mentzer, Steven J et al. (2017) Alveolar septal patterning during compensatory lung growth: Part II the effect of parenchymal pressure gradients. J Theor Biol 421:168-178
Bennett, Robert D; Ysasi, Alexandra B; Wagner, Willi L et al. (2017) Deformation-induced transitional myofibroblasts contribute to compensatory lung growth. Am J Physiol Lung Cell Mol Physiol 312:L79-L88
Gibney, Barry C; Wagner, Willi L; Ysasi, Alexandra B et al. (2017) Structural and functional evidence for the scaffolding effect of alveolar blood vessels. Exp Lung Res 43:337-346
Valenzuela, Cristian D; Wagner, Willi L; Bennett, Robert D et al. (2017) Extracellular Assembly of the Elastin Cable Line Element in the Developing Lung. Anat Rec (Hoboken) 300:1670-1679
Tsuda, Akira; Venkata, Nagarjun Konduru (2016) The role of natural processes and surface energy of inhaled engineered nanoparticles on aggregation and corona formation. NanoImpact 2:38-44
Haber, Shimon; Weisbord, Michal; Mishima, Michiaki et al. (2016) Interstitial fluid flow of alveolar primary septa after pneumonectomy. J Theor Biol 400:118-28
Henry, Frank S; Tsuda, Akira (2016) Onset of alveolar recirculation in the developing lungs and its consequence on nanoparticle deposition in the pulmonary acinus. J Appl Physiol (1985) 120:38-54
Wagner, Willi; Bennett, Robert D; Ackermann, Maximilian et al. (2015) Elastin Cables Define the Axial Connective Tissue System in the Murine Lung. Anat Rec (Hoboken) 298:1960-8

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