|
|
|
|
WK Schmidt and HP Moore
University of California at Berkeley, Department of Molecular and Cell Biology 94720-3200, USA.
Newly synthesized prohormones and their processing enzymes transit through the same compartments before being packaged into regulated secretory granules. Despite this coordinated intracellular transport, prohormone processing does not occur until late in the secretory pathway. In the mouse pituitary AtT-20 cell line, conversion of pro- opiomelanocortin (POMC) to mature adrenocorticotropic hormone involves the prohormone convertase PC1. The mechanism by which this proteolytic processing is restricted to late secretory compartments is unknown; PC1 activity could be regulated by compartment-specific activators/inhibitors, or through changes in the ionic milieu that influence its activity. By arresting transport in a semi-intact cell system, we have addressed whether metabolically labeled POMC trapped in early secretory compartments can be induced to undergo conversion if the ionic milieu in these compartments is experimentally manipulated. Prolonged incubation of labeled POMC trapped in the endoplasmic reticulum or Golgi/trans-Golgi network did not result in processing, thereby supporting the theory that processing is normally a post- Golgi/trans-Golgi network event. However, acidification of these compartments allowed effective processing of POMC to the intermediate and mature forms. The observed processing increased sharply at a pH below 6.0 and required millimolar calcium, regardless of the compartment in which labeled POMC resided. These conditions also resulted in the coordinate conversion of PC1 from the 84/87 kDa into the 74-kDa and 66-kDa forms. We propose that POMC processing is predominantly restricted to acidifying secretory granules, and that a change in pH within these granules is both necessary and sufficient to activate POMC processing.
This article has been cited by other articles:
![]() |
M. Perello, R. Stuart, and E. A. Nillni Prothyrotropin-releasing Hormone Targets Its Processing Products to Different Vesicles of the Secretory Pathway J. Biol. Chem., July 18, 2008; 283(29): 19936 - 19947. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. D. Dikeakos and T. L. Reudelhuber Sending proteins to dense core secretory granules: still a lot to sort out J. Cell Biol., April 23, 2007; 177(2): 191 - 196. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Kim, M. C. Gondre-Lewis, I. Arnaoutova, and Y. P. Loh Dense-Core Secretory Granule Biogenesis Physiology, April 1, 2006; 21(2): 124 - 133. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. E. Bell, T. J. McDonald, and D. A. Myers Proopiomelanocortin Processing in the Anterior Pituitary of the Ovine Fetus after Lesion of the Hypothalamic Paraventricular Nucleus Endocrinology, June 1, 2005; 146(6): 2665 - 2673. [Abstract] [Full Text] [PDF] |
||||
![]() |
M.-J. Lacombe, C. Mercure, J. D. Dikeakos, and T. L. Reudelhuber Modulation of Secretory Granule-targeting Efficiency by Cis and Trans Compounding of Sorting Signals J. Biol. Chem., February 11, 2005; 280(6): 4803 - 4807. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Nakamura, S. Tanaka, Y. Teko, K. Mitsui, and H. Kanazawa Four Na+/H+ Exchanger Isoforms Are Distributed to Golgi and Post-Golgi Compartments and Are Involved in Organelle pH Regulation J. Biol. Chem., January 14, 2005; 280(2): 1561 - 1572. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Paroutis, N. Touret, and S. Grinstein The pH of the Secretory Pathway: Measurement, Determinants, and Regulation Physiology, August 1, 2004; 19(4): 207 - 215. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Halaban, R. S. Patton, E. Cheng, S. Svedine, E. S. Trombetta, M. L. Wahl, S. Ariyan, and D. N. Hebert Abnormal Acidification of Melanoma Cells Induces Tyrosinase Retention in the Early Secretory Pathway J. Biol. Chem., April 19, 2002; 277(17): 14821 - 14828. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. A. Eaton, M. Haugwitz, D. Lau, and H.-P. H. Moore Biogenesis of Regulated Exocytotic Carriers in Neuroendocrine Cells J. Neurosci., October 1, 2000; 20(19): 7334 - 7344. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Kuliawat, D. Prabakaran, and P. Arvan Proinsulin Endoproteolysis Confers Enhanced Targeting of Processed Insulin to the Regulated Secretory Pathway Mol. Biol. Cell, June 1, 2000; 11(6): 1959 - 1972. [Abstract] [Full Text] |
||||
![]() |
A. Bruzzaniti, R. Marx, and R. E. Mains Activation and Routing of Membrane-tethered Prohormone Convertases 1 and 2 J. Biol. Chem., August 27, 1999; 274(35): 24703 - 24713. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. J. Fernandez, M. Haugwitz, B. Eaton, and H.-P. H. Moore Distinct Molecular Events during Secretory Granule Biogenesis Revealed by Sensitivities to Brefeldin A Mol. Biol. Cell, November 1, 1997; 8(11): 2171 - 2185. [Abstract] [Full Text] |
||||
![]() |
R. S. Taylor, S. M. Jones, R. H. Dahl, M. H. Nordeen, and K. E. Howell Characterization of the Golgi Complex Cleared of Proteins in Transit and Examination of Calcium Uptake Activities Mol. Biol. Cell, October 1, 1997; 8(10): 1911 - 1931. [Abstract] [Full Text] |
||||
![]() |
I. Jutras, N. G. Seidah, T. L. Reudelhuber, and V. Brechler Two Activation States of the Prohormone Convertase PC1 in the Secretory Pathway J. Biol. Chem., June 13, 1997; 272(24): 15184 - 15188. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. M. Wu, M. Grabe, S. Adams, R. Y. Tsien, H.-P. H. Moore, and T. E. Machen Mechanisms of pH Regulation in the Regulated Secretory Pathway J. Biol. Chem., August 24, 2001; 276(35): 33027 - 33035. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. C. Bell-Parikh, B. A. Eipper, and R. E. Mains Response of an Integral Granule Membrane Protein to Changes in pH J. Biol. Chem., August 3, 2001; 276(32): 29854 - 29863. [Abstract] [Full Text] [PDF] |
||||