February 1993
Volume 34, Issue 2
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Articles  |   February 1993
Plasma membrane internalization and recycling in rabbit lacrimal acinar cells.
Author Affiliations
  • R W Lambert
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • C A Maves
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • J P Gierow
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • R L Wood
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
  • A K Mircheff
    Department of Physiology and Biophysics, University of Southern California School of Medicine, Los Angeles 90033.
Investigative Ophthalmology & Visual Science February 1993, Vol.34, 305-316. doi:
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    • Get Citation

      R W Lambert, C A Maves, J P Gierow, R L Wood, A K Mircheff; Plasma membrane internalization and recycling in rabbit lacrimal acinar cells.. Invest. Ophthalmol. Vis. Sci. 1993;34(2):305-316.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

PURPOSE: The purpose of this study was to examine internalization and recycling of plasma membrane constituents in lacrimal gland acinar cells. METHODS: Acinar cells were isolated from rabbit lacrimal glands. Surface-expressed reactive groups were biotinylated at 4 degrees C with sulfo-N-hydroxysuccinimidyl-biotin. Incorporated biotin was then labeled with avidin-horseradish peroxidase complex for light microscopy, with avidin-lucifer yellow conjugate for fluorescence microscopy, and quantitative fluorometry, and with avidin-ferritin conjugate for electron microscopy. RESULTS: At 4 degrees C labels remained at the surfaces of intact cells. Surface avidin-lucifer yellow decreased markedly, giving way to punctate cytoplasmic labeling, on warming to 37 degrees C. Electron microscopy of cells warmed after labeling with avidin-ferritin revealed ferritin in smooth vesicles underlying the plasma membranes, in vesicles adjacent to Golgi membranes, and in multivesicular bodies. Incubation at 37 degrees C before chilling and labeling with avidin-lucifer yellow decreased the cells' capacity to bind avidin-lucifer yellow by 95%, with t0.5 < 0.5 min. If cells were then incubated with avidin-lucifer yellow at 37 degrees C, they took up the marker with a time course that indicated that 60% of the initial biotin either recycled back to the plasma membrane or remained in intracellular compartments that could be reached by endocytosed extracellular fluid. Internalized biotin communicated with extracellular avidin-lucifer yellow with a t0.5 of 2 min, and this process was accelerated by carbachol at concentrations of 10 mumol/l and 1 mmol/l. CONCLUSIONS: Acinar cell plasma membrane constituents participate in an ongoing, secretagogue-modulated recycling traffic between small surface-expressed pools and 10- to 20-fold larger intracellular pools.

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