» Articles » PMID: 31584728

Lymphatic-to-blood Vessel Transition in Adult Microvascular Networks: A Discovery Made Possible by a Top-down Approach to Biomimetic Model Development

Overview
Date 2019 Oct 5
PMID 31584728
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Emerging areas of vascular biology focus on lymphatic/blood vessel mispatterning and the regulation of endothelial cell identity. However, a fundamental question remains unanswered: Can lymphatic vessels become blood vessels in adult tissues? Leveraging a novel tissue culture model, the objective of this study was to track lymphatic endothelial cell fate over the time course of adult microvascular network remodeling.

Methods: Cultured adult Wistar rat mesenteric tissues were labeled with BSI-lectin and time-lapse images were captured over five days of serum-stimulated remodeling. Additionally, rat mesenteric tissues on day 0 and day 3 and 5 post-culture were labeled for PECAM + LYVE-1 or PECAM + podoplanin.

Results: Cultured networks were characterized by increases in blood capillary sprouting, lymphatic sprouting, and the number of lymphatic/blood vessel connections. Comparison of images from the same network regions identified incorporation of lymphatic vessels into blood vessels. Mosaic lymphatic/blood vessels contained lymphatic marker positive and negative endothelial cells.

Conclusions: Our results reveal the ability for lymphatic vessels to transition into blood vessels in adult microvascular networks and discover a new paradigm for investigating lymphatic/blood endothelial cell dynamics during microvascular remodeling.

Citing Articles

A Novel Ex Vivo Tumor Spheroid-Tissue Model for Investigating Microvascular Remodeling and Lymphatic Blood Vessel Plasticity.

Lampejo A, Lightsey S, Gomes M, Nguyen C, Siemann D, Sharma B Ann Biomed Eng. 2024; 52(9):2457-2472.

PMID: 38796670 DOI: 10.1007/s10439-024-03535-8.


Lymphatic/blood vessel plasticity: motivation for a future research area based on present and past observations.

Lampejo A, Ghavimi S, Hagerling R, Agarwal S, Murfee W Am J Physiol Heart Circ Physiol. 2022; 324(1):H109-H121.

PMID: 36459445 PMC: 9829479. DOI: 10.1152/ajpheart.00612.2022.


The Microvascular-Lymphatic Interface and Tissue Homeostasis: Critical Questions That Challenge Current Understanding.

Lampejo A, Jo M, Murfee W, Breslin J J Vasc Res. 2022; 59(6):327-342.

PMID: 36315992 PMC: 9780194. DOI: 10.1159/000525787.


A Challenge for Engineering Biomimetic Microvascular Models: How do we Incorporate the Physiology?.

Lampejo A, Hu N, Lucas D, Lomel B, Nguyen C, Dominguez C Front Bioeng Biotechnol. 2022; 10:912073.

PMID: 35795159 PMC: 9252339. DOI: 10.3389/fbioe.2022.912073.


The Internal Conduit System of the Swine Inverted Lymph Node.

Dubreil L, Ledevin M, Hervet C, Menard D, Philippe C, Michel F Front Immunol. 2022; 13:869384.

PMID: 35734172 PMC: 9207403. DOI: 10.3389/fimmu.2022.869384.


References
1.
Bruyere F, Melen-Lamalle L, Blacher S, Roland G, Thiry M, Moons L . Modeling lymphangiogenesis in a three-dimensional culture system. Nat Methods. 2008; 5(5):431-7. DOI: 10.1038/nmeth.1205. View

2.
Kaunas R, Kang H, Bayless K . Synergistic Regulation of Angiogenic Sprouting by Biochemical Factors and Wall Shear Stress. Cell Mol Bioeng. 2012; 4(4):547-559. PMC: 3254182. DOI: 10.1007/s12195-011-0208-5. View

3.
Azimi M, Motherwell J, Murfee W . An Ex Vivo Method for Time-Lapse Imaging of Cultured Rat Mesenteric Microvascular Networks. J Vis Exp. 2017; (120). PMC: 5408852. DOI: 10.3791/55183. View

4.
Martinez-Corral I, Ulvmar M, Stanczuk L, Tatin F, Kizhatil K, John S . Nonvenous origin of dermal lymphatic vasculature. Circ Res. 2015; 116(10):1649-54. DOI: 10.1161/CIRCRESAHA.116.306170. View

5.
Maruyama K, Ii M, Cursiefen C, Jackson D, Keino H, Tomita M . Inflammation-induced lymphangiogenesis in the cornea arises from CD11b-positive macrophages. J Clin Invest. 2005; 115(9):2363-72. PMC: 1193872. DOI: 10.1172/JCI23874. View