Localization of inositol 1,4,5-trisphosphate receptors in mouse retinal ganglion cells

✍ Scribed by Oloruntoyin A. Mafe; Elaine V. Gregg; Wanda E. Medina-Ortiz; Peter Koulen

• Publisher: John Wiley and Sons
• Year: 2006
• Tongue: English
• Weight: 280 KB
• Volume: 84
• Category: Article
• ISSN: 0360-4012
• DOI: 10.1002/jnr.21090

✦ Synopsis

Abstract

Inositol 1,4,5‐trisphosphate receptors (IP~3~R) are ligand‐gated intracellular Ca^2+^channels that mediate release of Ca^2+^ from intracellular stores into the cytosol on activation by second messenger IP~3~. Similarly, IP~3~R mediated changes in cytosolic Ca^2+^ concentrations control neuronal functions ranging from synaptic transmission to differentiation and apoptosis. IP~3~R‐generated cytosolic Ca^2+^ transients also control intracellular Ca^2+^ release and subsequent retinal ganglion cell (RGC) physiology and pathophysiology. The distribution of IP~3~R isotypes in primary adult mouse RGC cultures was determined to identify molecular substrates of IP~3~R mediated signaling in these neurons. Immunocytochemical labeling of IP~3~Rs in retinal sections and cultured RGCs was carried out using isoform specific antibodies and was detected with fluorescence microscopy. RGCs were identified by the use of morphologic criteria and RGC‐specific immunocytochemical markers, neurofilament 68 kDa, Thy 1.1, and Thy 1.2. RGC morphology and immunoreactivity to neurofilament 68 kDa and Thy 1.1 or Thy 1.2 were identified in both RGC primary cultures and tissue cryosections. RGCs showed localization on intracellular membranes with a differential distribution of IP~3~R isoforms 1, 2, and 3. IP~3~R Types 1 and 3 were detected intracellularly throughout the cell whereas Type 2 was expressed predominantly in soma. Expression of all three IP~3~Rs by RGCs indicates that all IP~3~R types potentially play a role in Ca^2+^ homeostasis and Ca^2+^ signaling in these cells. Differential localization of IP~3~ receptor subtypes in combination with biophysical properties of IP~3~R types may be an important molecular mechanism by which RGCs organize their cytosolic Ca^2+^ signals. © 2006 Wiley‐Liss, Inc.