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Vol. 11, Issue 11, 3925-3935, November 2000
Department of Cell Biology, University of Texas Southwestern
Medical Center, Dallas, Texas 75390
FKBP65 (65-kDa FK506-binding protein) is a member of the highly
conserved family of intracellular receptors called immunophilins. All
have the property of peptidyl-prolyl cis-trans
isomerization, and most have been implicated in folding and trafficking
events. In an earlier study, we identified that FKBP65 associates with the extracellular matrix protein tropoelastin during its transport through the cell. In the present study, we have carried out a detailed investigation of the subcellular localization of FKBP65 and
its relationship to tropoelastin. Using subcellular fractionation, Triton X-114 phase separation, protease protection assays, and immunofluorescence microscopy (IF), we have identified that FKBP65 is
contained within the lumen of the endoplasmic reticulum (ER). Subsequent IF studies colocalized FKBP65 with tropoelastin and showed
that the two proteins dissociate before reaching the Golgi apparatus.
Immunohistochemical localization of FKBP65 in developing lung showed
strong staining of vascular and airway smooth muscle cells. Similar
areas stained positive for the presence of elastic fibers in the
extracellular matrix. The expression of FKBP65 was investigated during
development as tropoelastin is not expressed in adult tissues.
Tissue-specific expression of FKBP65 was observed in 12-d old mouse
tissues; however, the pattern of expression of FKBP65 was not
restricted to those tissues expressing tropoelastin. This suggests that
additional ligands for FKBP65 likely exist within the ER. Remarkably,
in the adult tissues examined, FKBP65 expression was absent or barely
detectable. Taken together, these results support an ER-localized
FKBP65-tropoelastin interaction that occurs specifically during growth
and development of tissues.
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