<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Spurgin S</submitter><funding>American Thoracic Society</funding><funding>Pediatric Scientist Development Program</funding><funding>NICHD NIH HHS</funding><funding>Fondation Leducq</funding><funding>NHLBI NIH HHS</funding><funding>National Heart, Lung, and Blood Institute</funding><funding>NCI NIH HHS</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><funding>NIH HHS</funding><pagination>1187-1202</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12353473</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>254(11)</volume><pubmed_abstract>Cilia are specialized structures found on a variety of mammalian cells, with variable roles in the transduction of mechanical and biological signals (by primary cilia, PC), as well as in the generation of fluid flow (by motile cilia). Their critical role in the establishment of a left-right axis in early development is well described, as well as in the defense immune function of multiciliated upper airway epithelium. By contrast, detailed analysis of the ciliary status of specific cell types during organogenesis and postnatal development has received less attention. In this study, we investigate the progression of ciliary status within the endothelium and mesenchyme of the lung. Remarkably, we find that pulmonary endothelial cells (ECs) lack PC at all stages of development, except in low numbers in the proximal portions of older pulmonary arteries. Mesenchymal cells, by contrast, widely exhibit PC in early development, and a large subset of PDGFRα+ fibroblasts maintain PC into adulthood. The dynamic and differential ciliation of multiple cellular populations in the developing lung both challenges prior assertions that PC are found on all cells and highlights a need to understand their spatiotemporal functions.</pubmed_abstract><journal>Developmental dynamics : an official publication of the American Association of Anatomists</journal><pubmed_title>Dynamics of primary cilia in endothelial and mesenchymal cells throughout mouse lung development.</pubmed_title><pmcid>PMC12353473</pmcid><funding_grant_id>R00HL141684</funding_grant_id><funding_grant_id>R35 HL140014</funding_grant_id><funding_grant_id>K12 HD000850</funding_grant_id><funding_grant_id>3K12HD000850-38S1</funding_grant_id><funding_grant_id>R01 HL113498</funding_grant_id><funding_grant_id>R35 GM144136</funding_grant_id><funding_grant_id>R00 HL141684</funding_grant_id><funding_grant_id>23-24PACDA12</funding_grant_id><funding_grant_id>S10 OD021685</funding_grant_id><funding_grant_id>R35HL140014</funding_grant_id><funding_grant_id>HL113498</funding_grant_id><funding_grant_id>R01 HL126518</funding_grant_id><funding_grant_id>N35GM119461</funding_grant_id><funding_grant_id>1R35GM144136</funding_grant_id><funding_grant_id>21CVD03</funding_grant_id><funding_grant_id>P30 CA060553</funding_grant_id><funding_grant_id>23‐24PACDA12</funding_grant_id><funding_grant_id>3K12HD000850‐38S1</funding_grant_id><funding_grant_id>R35 GM119461</funding_grant_id><pubmed_authors>Spurgin S</pubmed_authors><pubmed_authors>Chaudhry FN</pubmed_authors><pubmed_authors>Michki SN</pubmed_authors><pubmed_authors>Iruela-Arispe ML</pubmed_authors><pubmed_authors>Nguimtsop AM</pubmed_authors><pubmed_authors>Zepp JA</pubmed_authors><pubmed_authors>Mukhopadhyay S</pubmed_authors><pubmed_authors>Cleaver O</pubmed_authors><pubmed_authors>Salvador J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Dynamics of primary cilia in endothelial and mesenchymal cells throughout mouse lung development.</name><description>Cilia are specialized structures found on a variety of mammalian cells, with variable roles in the transduction of mechanical and biological signals (by primary cilia, PC), as well as in the generation of fluid flow (by motile cilia). Their critical role in the establishment of a left-right axis in early development is well described, as well as in the defense immune function of multiciliated upper airway epithelium. By contrast, detailed analysis of the ciliary status of specific cell types during organogenesis and postnatal development has received less attention. In this study, we investigate the progression of ciliary status within the endothelium and mesenchyme of the lung. Remarkably, we find that pulmonary endothelial cells (ECs) lack PC at all stages of development, except in low numbers in the proximal portions of older pulmonary arteries. Mesenchymal cells, by contrast, widely exhibit PC in early development, and a large subset of PDGFRα+ fibroblasts maintain PC into adulthood. The dynamic and differential ciliation of multiple cellular populations in the developing lung both challenges prior assertions that PC are found on all cells and highlights a need to understand their spatiotemporal functions.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-05T14:29:02.153Z</modification><creation>2026-05-17T03:12:25.864Z</creation></dates><accession>S-EPMC12353473</accession><cross_references><pubmed>40055935</pubmed><doi>10.1002/dvdy.70008</doi></cross_references></HashMap>