Neuronal filopodium formation induced by the membrane glycoprotein M6a (Gpm6a) is facilitated by coronin‐1a, Rac1, and p21‐activated kinase 1 (Pak1)

• Published in: Journal of neurochemistry 2016-04, Vol.137 (1), p.46-61
• Main Authors: Alvarez Juliá, Anabel, Frasch, Alberto C., Fuchsova, Beata
• Format: Article
• Language: English
• Subjects: Actins - analysis; Animals; Cells, Cultured; Coronin‐1a; Cytoskeleton; Down-Regulation; filopodium; Genes, Reporter; Glycoproteins; hippocampal neuron; Hippocampus - cytology; Kinases; membrane glycoprotein M6a; Membrane Glycoproteins - physiology; Microfilament Proteins - genetics; Microfilament Proteins - physiology; Nerve Tissue Proteins - antagonists & inhibitors; Nerve Tissue Proteins - physiology; Neurochemistry; Neurons - ultrastructure; Organelle Biogenesis; p21-Activated Kinases - physiology; Primary Cell Culture; Pseudopodia - physiology; rac1 GTP-Binding Protein - antagonists & inhibitors; rac1 GTP-Binding Protein - physiology; Ras‐related C3 botulinum toxin substrate 1 (Rac1); rat; Rats; Rats, Sprague-Dawley; RNA, Small Interfering - genetics; Rodents; Signal Transduction - drug effects; Signal Transduction - physiology
• ISSN: 0022-3042; 1471-4159
• DOI: 10.1111/jnc.13552

Stress‐responsive neuronal membrane glycoprotein M6a (Gpm6a) functions in neurite extension, filopodium and spine formation and synaptogenesis. The mechanisms of Gpm6a action in these processes are incompletely understood. Previously, we identified the actin regulator coronin‐1a (Coro1a) as a putative Gpm6a interacting partner. Here, we used co‐immunoprecipitation assays with the anti‐Coro1a antibody to show that Coro1a associates with Gpm6a in rat hippocampal neurons. By immunofluorescence microscopy, we demonstrated that in hippocampal neurons Coro1a localizes in F‐actin‐enriched regions and some of Coro1a spots co‐localize with Gpm6a labeling. Notably, the over‐expression of a dominant‐negative form of Coro1a as well as its down‐regulation by siRNA interfered with Gpm6a‐induced filopodium formation. Coro1a is known to regulate the plasma membrane translocation and activation of small GTPase Rac1. We show that Coro1a co‐immunoprecipitates with Rac1 together with Gpm6a. Pharmacological inhibition of Rac1 resulted in a significant decrease in filopodium formation by Gpm6a. The same was observed upon the co‐expression of Gpm6a with the inactive GDP‐bound form of Rac1. In this case, the elevated membrane recruitment of GDP‐bound Rac1 was detected as well. Moreover, the kinase activity of the p21‐activated kinase 1 (Pak1), a main downstream effector of Rac1 that acts downstream of Coro1a, was required for Gpm6a‐induced filopodium formation. Taken together, our results provide evidence that a signaling pathway including Coro1a, Rac1, and Pak1 facilitates Gpm6a‐induced filopodium formation. Formation of filopodia by membrane glycoprotein M6a (Gpm6a) requires actin regulator coronin‐1a (Coro1a), known to regulate plasma membrane localization and activation of Rac1 and its downstream effector Pak1. Coro1a associates with Gpm6a. Blockage of Coro1a, Rac1, or Pak1 interferes with Gpm6a‐induced filopodium formation. Moreover, Gpm6a facilitates Rac1 membrane recruitment. Altogether, a mechanistic insight into the process of Gpm6a‐induced neuronal filopodium formation is provided. Formation of filopodia by membrane glycoprotein M6a (Gpm6a) requires actin regulator coronin‐1a (Coro1a), known to regulate plasma membrane localization and activation of Rac1 and its downstream effector Pak1. Coro1a associates with Gpm6a. Blockage of Coro1a, Rac1, or Pak1 interferes with Gpm6a‐induced filopodium formation. Moreover, Gpm6a facilitates Rac1 membrane recruitment. Altogether, a