Elsevier

Neuroscience

Volume 142, Issue 4, 3 November 2006, Pages 1055-1069
Neuroscience

Cellular neuroscience
Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation

https://doi.org/10.1016/j.neuroscience.2006.07.054Get rights and content

Abstract

Perineuronal nets (PNs) are lattice-like condensations of the extracellular matrix (ECM) that envelop synapses and decorate the surface of subsets of neurons in the CNS. Previous work has suggested that, despite the fact that PNs themselves are not visualized until later in development, some PN component molecules are expressed in the rodent CNS even before synaptogenesis. In the adult mammalian brain, monoclonal antibody Cat-315 recognizes a glycoform of aggrecan, a major component of PNs. In primary cortical cultures, a Cat-315-reactive chondroitin sulfate proteoglycan (CSPG) is also expressed on neuronal surfaces and is secreted into culture media as early as 24 h after plating. In this study, we show that in primary cortical cultures, the Cat-315 CSPG detected in early neural development is expressed in extrasynaptic sites prior to synapse formation. This suggests that ECM components in the CNS, as in the neuromuscular junction (NMJ), may prepattern neuronal surfaces prior to innervation. We further show that while the Cat-315-reactive carbohydrate decorates aggrecan in the adult, it decorates a different CSPG in the developing CNS. Using receptor protein tyrosine phosphatase beta (RPTPβ/protein tyrosine phosphatase zeta) knock-out mice and immunoprecipitation techniques, we demonstrate here that in the developing rodent brain Cat-315 recognizes RPTPβ isoforms. Our further examination of the Cat-315 epitope suggests that it is an O-mannose linked epitope in the HNK-1 family. The presence of the Cat-315 reactive carbohydrate on different PN components—RPTPβ and aggrecan—at different stages of synapse development suggests a potential role for this neuron-specific carbohydrate motif in synaptogenesis.

Section snippets

Antibodies

Cat-315 has been previously characterized (Lander et al., 1997). Rabbit polyclonal anti-synaptophysin was a gift from Dr. Pietro de Camilli (Cell Biology Department, Yale University Medical School, New Haven, CT, USA). Mouse monoclonal anti-phosphacan (mAb 5210) and anti-synaptophysin (clone SY35) antibodies were purchased from Chemicon (Temecula, CA, USA). The mouse monoclonal antibody3F8 developed by Dr. Margolis was obtained from the Developmental Hybridoma Bank, developed under the auspices

Neuronal cell-surface expression of an early-expressed Cat-315 proteoglycan precedes the development of synaptic contacts

Our previous work has shown that, while the monoclonal antibody Cat-315 detects PNs in the adult cerebral cortex, it also detects a cell-surface CSPG far in advance of net development. In E19 and P0 rodent brain, Cat-315 staining is diffuse in the cortical parenchyma but is prominent in fiber tracts (data not shown).

To further investigate the early expression of Cat-315, we investigated cultured cortical neurons prepared from E16 or P0 rats. As had been previously demonstrated, we found

Discussion

We demonstrate here that Cat-315-reactive puncta decorate the surface of primary neuronal cultures within 24 h after plating, well before the formation of synapses. Interestingly, as synapses develop in culture, synaptic markers are never co-localized with Cat-315 puncta. Instead, Cat-315 puncta are always found adjacent to sites of synaptic contact. The finding that the Cat-315 puncta are detected early in development and are found exclusively in extra- or non-synaptic sites, suggests a

Acknowledgments

This work was supported by NIH grant EY06511 (to S.H.) and NSF postdoctoral minority fellowship (to M.R.D.). We thank Smaragda Lamprianou for preparation of tissue samples from the RPTPβ knockout mice. We also thank Mariano Viapiano and Gail Kelly for advice, discussion, and comments during the preparation of this manuscript.

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    Present address: Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139–4307, USA.

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