Fetal liver monocytes seed the lungs between embryonic day 14.5 and birth.2 These cells then differentiate into prealveolar macrophages and acquire PPAR-γ expression through GM-CSFR signaling.3 These prealveolar macrophages then translocate and engraft into the alveolar space in the first week of life, where they develop into terminally differentiated alveolar macrophages. In LPL-deficient mice, the translocation and the engraftment into the alveolar space are impaired (compare left and right panel), resulting in a severe reduction in number of alveolar macrophages and in an increased susceptibility to pneumococcal infection.

Fetal liver monocytes seed the lungs between embryonic day 14.5 and birth. These cells then differentiate into prealveolar macrophages and acquire PPAR-γ expression through GM-CSFR signaling. These prealveolar macrophages then translocate and engraft into the alveolar space in the first week of life, where they develop into terminally differentiated alveolar macrophages. In LPL-deficient mice, the translocation and the engraftment into the alveolar space are impaired (compare left and right panel), resulting in a severe reduction in number of alveolar macrophages and in an increased susceptibility to pneumococcal infection.

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