Ultrastructural analysis of VIP internalization in rat beta- and acinar cells in situ

Am J Physiol. 1989 Apr;256(4 Pt 1):G689-97. doi: 10.1152/ajpgi.1989.256.4.G689.

Abstract

We perfused the pancreas with 125I-labeled vasoactive intestinal peptide (VIP) to follow the concomitant distribution of radioactivity in beta- and acinar cells as a function of time. This distribution was quantitated by computer-assisted analysis of high-resolution video autoradiographs. Density labeling was expressed as normalized specific activity (disintegration density per volume density). Immediately after a 4-min perfusion of 125I-VIP, labeling in beta-cells was mainly concentrated on the cell surface and peripheral tubules and vesicles. After three 30-s pulses of 125I-VIP, separated by intervals of 3.5 min of buffer perfusion, lysosome-like structures were heavily labeled. When VIP internalization was prolonged, labeling was similar to that observed with the 4-min perfusion, indicating a high VIP disposal rate in the lysosome-like structures. In acinar cells, labeling persisted on the surface and the early vacuolar system. We conclude the following: 1) an active endocytotic system, linked to the transport and sorting of a neuromediator, is present in beta-cells; and 2) the differences between the distribution of labeling in acinar and beta-cells suggest that the regulation of VIP internalization is tissue specific.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding, Competitive
  • Cell Membrane / metabolism
  • Chromatography, High Pressure Liquid
  • Endocytosis
  • Golgi Apparatus / metabolism
  • Kinetics
  • Lysosomes / metabolism
  • Male
  • Microscopy, Electron
  • Organelles / metabolism
  • Pancreas / metabolism
  • Pancreas / ultrastructure*
  • Rats
  • Rats, Inbred Strains
  • Vacuoles / metabolism
  • Vasoactive Intestinal Peptide / metabolism*

Substances

  • Vasoactive Intestinal Peptide