Many studies have been carried out to investigate the occurrence and distribution of telocytes (TCs) in many
organs. However, their morphological development is still unclear. This study was performed to demonstrate
the morphological development of TCs in rabbits' lung from fetal to postnatal life using light-, electronmicroscopy,
immunohistochemistry, morphometrical and statistical analysis. During the fetal life, these cells
formed an extensive network of telopodes (Tps) which were in close contact with developing alveoli,
bronchioles, stem cells and many other interstitial components. In addition, the TCs' number was significantly
increased around the neocapillaries in fetal lung. In the fetal life, TCs were stellate in shape and characterized by
large cell bodies and many short Tps that contained abundant rER, mitochondria, and ribosomes. By gradual
increasing of ages, TCs were spindle in shape with two Tps contained a massive amount of secretory structures
(exosomes, ectosomes, and multivesicular bodies). Moreover, TCs in postnatal lung showed a significant
decrease in number and diameter of their cell bodies and a significant increase in the length of Tps compared
with those in fetal life. The TCs contributed with pneumocytes and endothelium in the formation of air-blood
barrier. The TCs' immunohistochemical profiles for CD34, vimentin, c-kit, connexin 43, vascular endothelial
growth factor (VEGF), and neuron- specific enolase (NSE) differed between ages during the lung development.
This study provided an evidence that TCs contributed to angiogenesis, the formation of the air-blood barrier,
lung organization, and development.
Research Abstract	
              Research Date	
              Research Department	
              
          Research Journal	
              Developmental Biology
          Research Member	
          
      Research Publisher	
              Elseiver
          Research Rank	
              Q2
          Research Vol	
              443
          Research Website	
              https://doi.org/10.1016/j.ydbio.2018.09.010
          Research Year	
              2018