Lymph transport occurs against a hydrostatic pressure gradient and thus relies critically on the intrinsic contractile function of lymphatic muscle, the ?active lymphatic pump?. Failure of this pump is associated with many types of lymphedema. Little is known about why lymphatic vessels become dysfunctional, but clinical studies reveal an elevated lymphatic diastolic pressure, enlarged diameter, impaired or absent contractions, and incompetent valves. These findings point to both pacemaker and valve dysfunction as underlying causes. This R01 renewal continues to address the ionic mechanisms of pacemaking in lymphatic vessels, with the ultimate goal of developing methods to treat pacemaker and contractile dysfunction in lymphedema. In the previous funding period genetic methods were used to assess the roles of multiple ion channels in mouse lymphatic smooth muscle and a critical role for Ano1 (TMEM16A) was found. SM-specific deletion resulted in a 3-4-fold reduction in pacemaking frequency and blunting or abolition of the increase in frequency in response to pressure elevation. This proposal continues to use tissue-specific and global mouse KO models to answer questions about ion channels that act in concert with Ano1 to initiate pacemaking in lymphatic smooth muscle cells (LMCs). It addresses not only how Ano1 is activated but also pressure-sensing mechanisms through mechanosensitive ion channels or G-protein-coupled receptors (GPCRs). Optogenetic tools will be used extensively for measuring intracellular Ca2+ events, uncaging Ca2+ or IP3 and triggering depolarization with channel rhodopsin. The central hypothesis is that a membrane oscillator generates a repetitive cycle of depolarization/repolarization to trigger lymphatic action potentials (APs) and this cycle is modulated by mechanosensitive ionic conductances and by G?q/11-mediated IP3 production / Ca2+ release. This hypothesis will be tested with 2 experimental aims and a numerical modeling aim to aid in the interpretation and integration of the underlying mechanisms: 1) Elucidate the Ca2+ sensitive ionic mechanisms that facilitate initiation of the lymphatic AP. Is another Ca2+-activated ion channel acting in combination with Ano1 to provide depolarization prior to AP firing? Is the slope of diastolic depolarization near the AP threshold determined by Ca2+ release events? Is a Ca2+-independent membrane oscillator involving HCN and Kv7 channels acting in combination with Ano1 as part of the pacemaking mechanism? 2) Determine the pressure- sensitive ionic mechanisms that regulate lymphatic pacemaking. Do mechanosensitive GPCRs coupled to G?q/11 drive IP3 production to regulate Ano1? Do mechanosensitive ion channels modulate depolarization or repolarization? In parallel, 3) Numerical models will be used to predict and verify ionic mechanisms that govern pacemaking, including the shape of the LMC action potential, the effect of pressure on diastolic depolarization, factors determining pacemaker initiation sites, and properties of rectifying myoendothelial junctions that might prevent current shunting to the endothelial layer but allow endothelial modulation of LMCs.

Public Health Relevance

Lymphedema affects over 10 million people annually in the USA, yet little is known about how and why lymphatic vessels become dysfunctional in lymphedema. Like the heart, active lymphatic pumping is driven by an intrinsic pacemaker system in the lymphatic vessel wall, which fails in many forms of lymphedema. This project will uses multiple transgenic mouse models to uncover the calcium- and pressure-sensitive ionic mechanisms that control active lymphatic pumping with the goal that rescue of the failed lymph pump will be a new strategy for treating lymphatic dysfunction not only in lymphedema but in other diseases that have a component of lymphatic dysfunction.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL122578-06
Application #
10076844
Study Section
Hypertension and Microcirculation Study Section (HM)
Program Officer
Galis, Zorina S
Project Start
2015-04-01
Project End
2023-12-31
Budget Start
2021-01-01
Budget End
2021-12-31
Support Year
6
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of Missouri-Columbia
Department
Pharmacology
Type
Schools of Medicine
DUNS #
153890272
City
Columbia
State
MO
Country
United States
Zip Code
65211
Zawieja, Scott D; Castorena-Gonzalez, Jorge A; Scallan, Joshua P et al. (2018) Differences in L-type Ca2+ channel activity partially underlie the regional dichotomy in pumping behavior by murine peripheral and visceral lymphatic vessels. Am J Physiol Heart Circ Physiol 314:H991-H1010
Hald, Bjørn Olav; Castorena-Gonzalez, Jorge Augusto; Zawieja, Scott David et al. (2018) Electrical Communication in Lymphangions. Biophys J 115:936-949
Cha, Boksik; Geng, Xin; Mahamud, Md Riaj et al. (2018) Complementary Wnt Sources Regulate Lymphatic Vascular Development via PROX1-Dependent Wnt/?-Catenin Signaling. Cell Rep 25:571-584.e5
Zawieja, Scott D; Castorena-Gonzalez, Jorge A; Dixon, Brandon et al. (2017) Experimental Models Used to Assess Lymphatic Contractile Function. Lymphat Res Biol 15:331-342
Jamalian, Samira; Jafarnejad, Mohammad; Zawieja, Scott D et al. (2017) Demonstration and Analysis of the Suction Effect for Pumping Lymph from Tissue Beds at Subatmospheric Pressure. Sci Rep 7:12080
Jung, Eunson; Gardner, Daniel; Choi, Dongwon et al. (2017) Development and Characterization of A Novel Prox1-EGFP Lymphatic and Schlemm's Canal Reporter Rat. Sci Rep 7:5577
Bertram, C D; Macaskill, C; Davis, M J et al. (2017) Valve-related modes of pump failure in collecting lymphatics: numerical and experimental investigation. Biomech Model Mechanobiol 16:1987-2003
Behringer, Erik J; Scallan, Joshua P; Jafarnejad, Mohammad et al. (2017) Calcium and electrical dynamics in lymphatic endothelium. J Physiol 595:7347-7368
Davis, Michael J (2016) Is nitric oxide important for the diastolic phase of the lymphatic contraction/relaxation cycle? Proc Natl Acad Sci U S A 113:E105
Scallan, Joshua P; Zawieja, Scott D; Castorena-Gonzalez, Jorge A et al. (2016) Lymphatic pumping: mechanics, mechanisms and malfunction. J Physiol 594:5749-5768

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