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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The present protocol describes preparing and utilizing mouse precision-cut lung slices to assess the airway and intrapulmonary arterial smooth muscle contractility in a nearly in vivo milieu.

Abstract

Smooth muscle cells (SMC) mediate the contraction of the airway and the intrapulmonary artery to modify airflow resistance and pulmonary circulation, respectively, hence playing a critical role in the homeostasis of the pulmonary system. Deregulation of SMC contractility contributes to several pulmonary diseases, including asthma and pulmonary hypertension. However, due to limited tissue access and a lack of culture systems to maintain in vivo SMC phenotypes, molecular mechanisms underlying the deregulated SMC contractility in these diseases remain fully identified. The precision-cut lung slice (PCLS) offers an ex vivo model that circumvents these technical difficulties. As a live, thin lung tissue section, the PCLS retains SMC in natural surroundings and allows in situ tracking of SMC contraction and intracellular Ca2+ signaling that regulates SMC contractility. Here, a detailed mouse PCLS preparation protocol is provided, which preserves intact airways and intrapulmonary arteries. This protocol involves two essential steps before subjecting the lung lobe to slicing: inflating the airway with low-melting-point agarose through the trachea and infilling pulmonary vessels with gelatin through the right ventricle. The PCLS prepared using this protocol can be used for bioassays to evaluate Ca2+-mediated contractile regulation of SMC in both the airway and the intrapulmonary arterial compartments. When applied to mouse models of respiratory diseases, this protocol enables the functional investigation of SMC, thereby providing insight into the underlying mechanism of SMC contractility deregulation in diseases.

Introduction

Smooth muscle cell (SMC) is a major structural cell type in the lung, primarily residing in the media wall of airways and pulmonary vessels. SMCs contract to alter the luminal caliber, thus regulating air and blood flow1,2. Therefore, contractile regulation of SMCs is essential to maintain the homeostasis of air ventilation and pulmonary circulation. In contrast, aberrant SMC contractility provokes obstructive airway or pulmonary vascular diseases like asthma and pulmonary arterial hypertension. However, the functional assessment of lung SMCs has been challenged by limited access to the lung tissue, especially....

Protocol

All animal care was in accordance with the guidelines of the Institutional Animal Care and Use Committee of Massachusetts General Hospital. Wild-type C57/B6 male mice, 8 weeks of age, were used for the present study.

1. Experimental preparation

  1. Prepare the working solution.
    1. Prepare 1x Hank's Balanced Salt Solution (HBSS, with Ca2+ and Mg2+, and pH balanced with 20 mM HEPES, see Table of Materials). Use the HBSS.......

Representative Results

Mouse PCLS preparation preserving intact intrapulmonary airways and arteries
A 150 µm thick PCLS was observed under the inverted phase-contrast microscope. In mouse lungs, conductive airways are accompanied by intrapulmonary arteries, running from the hilus to the peripheral lung. A representative pulmonary airway-artery bundle in a mouse PCLS is shown in Figure 2B. The airway can be easily identified by cuboidal epithelial cells with active cilial beating lining .......

Discussion

The preparation of PCLS involves several critical steps. First, it is essential to inflate the lung lobe homogeneously to avoid the variation of tissue stiffness from uneven agarose distribution. As the liquid agarose rapidly gels in thin catheters or airways at a temperature below 37 °C, the resultant filling defect in the distal lung field could increase the disparity of lung tissue stiffness and cause tissue tearing during the vibratome section. Therefore, keeping the low-melting agarose solution at 42 °C in.......

Acknowledgements

This work is supported by NIH grants, K08135443 (Y.B), 1R01HL132991 (X.A).

....

Materials

NameCompanyCatalog NumberComments
1 mL syringeBD309626
15 mL sterile centrifuge tubesCelltreat229411
3 mL syringeBD309585
50 mL sterile centrifuge tubesCelltreat229422
Acetyl-beta-methacholineMillipore Sigma62-51-1
Antibiotic-anitmycoticThermo Fisher15240-062
CCD-cameraNikonNikon Ds-Ri2 camera
Cover glassessFisher Scientific12-548-5CP; 12-548-5PP
Cryogenic vialsFisher Scientific430488
Custom-built laser scanning confocal microscopeDetails in Reference 18
DMEM/F12Fisher ScientificMT-10-092-CM
Endothelin 1Millipore SigmaE7764
Fine dissecting scissorFisher ScientificNC9702861
Freezing containerSigma-AldrichC1562
Gelatin from porcine skinSigma-Aldrich9000-70-8
Hanks' Balanced Salt Solution (HBSS)Thermo Fisher14025092
Hemostatic forcepFisher Scientific16-100-117
HEPESThermo Fisher15630080
High vaccum silicone greaseFisher Scientific146355d
Isopropyl alcoholSigma-AldrichW292907-1KG-K
Metal washersHome Depot Product Authority800442Everbilt Flat Washers #10
Micro-dissecting forcepSigma-AldrichF4142
Needle scalp vein set (25 G)EXELINT26708
NOC-5Cayman Chemical16534
Nylon meshComponent SupplyU-CMN-300
Oregon green 488 BAPTA-1 AMLife Technologieso-6807
Phase-contrast microscopeNikonNikon Eclipse TS 100
Pluronic F-127Thermo FisherP-6867
Razor bladesPersonnaPersonna Double Edge Razor Blades in White Wrapper 100 count
SulfobromophthaleinSigma-AldrichS0252
SuperglueKrazy GlueKrazy Glue, All purpose
Ultrapure low melting point agaroseThermo Fisher16520050
VibratomePrecisionaryVF 310-0Z
Vibratome chilling blockPrecisionarySKU-VM-CB12.5-NC
Vibratome specimen tubePrecisionarySKU VF-SPS-VM-12.5-NC
Y shaped IV catheterBD383336BD Saf-T-Intima closed IV catheter

References

  1. Prakash, Y. S. Emerging concepts in smooth muscle contributions to airway structure and function: implications for health and disease. American Journal of Physiology Lung Cellular and Molecular Physiology. 311 (6), 1113-1140 (2016).
  2. Lechartier, B., et al.

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