Cell-cell communication in heterocellular cultures of alveolar epithelial cells

被引:47
作者
Isakson, BE
Seedorf, GJ
Lubman, RL
Evans, WH
Boitano, S
机构
[1] Univ Arizona, Ctr Hlth Sci, Dept Physiol, Arizona Resp Ctr, Tucson, AZ 85724 USA
[2] Univ Wyoming, Dept Zool & Physiol, Laramie, WY 82071 USA
[3] Univ So Calif, Keck Sch Med, Div Pulm & Crit Care Med, Los Angeles, CA USA
[4] Univ Wales Coll Med, Wales Heart Res Inst, Dept Biochem Med, Cardiff CF4 4XN, S Glam, Wales
关键词
D O I
10.1165/rcmb.2002-0281OC
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian alveolar epithelium is composed of alveolar type I (AT1) and alveolar type If (AT2) cells that together coordinate tissue function. We used a heterocellular culture model of AT1 and AT2 cells to determine pathways for intercellular signaling between these two phenotypes. Gap junction protein (connexin) profiles of AT1 and AT2 cells in heterocellular cultures were similar to those seen in rat lung alveolar sections. Dye coupling studies revealed functional gap junctions between and among each cell phenotype. Localized mechanical stimulation resulted in propagated changes of intracellular Ca2+ to AT1 or AT2 cells independent of the stimulated cell phenotype. Call communication that originated after AT1 cell stimulation was inhibited by gap junction blockers, but not by an inhibitor of extracellular nucleotide signaling (apyrase). Conversely, Ca2+ communication after stimulation of AT2 cells was not significantly reduced by gap junction inhibitors. However, apyrase significantly reduced Ca2+ communication from AT2 to AT1 cells, but not from AT2 to AT2 cells. In conclusion, AT1 and AT2 cells have unique connexin profiles that allow for functional coupling and distinct intercellular pathways for coordination of Ca2+ signaling.
引用
收藏
页码:552 / 561
页数:10
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