5 µm thick tissue sections of primary normal and LAM lungs (n=6 each, respectively) were stained in Mayer’s haematoxylin solution (Sigma-Aldrich, St. Louis, USA) for 10 min, washed, then differentiated with 0.25% acetic acid and in eosin solution. Sections were mounted using Vectashield mounting medium (Vector Laboratories, Burlingame, USA). Images were taken using Nikon Eclipse Ti-U inverted microscope.

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