RGD Reference Report - Protease-activated receptor subtype expression in developing eye and adult retina of the rat after optic nerve crush. - Rat Genome Database

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Protease-activated receptor subtype expression in developing eye and adult retina of the rat after optic nerve crush.

Authors: Rohatgi, T  Sedehizade, F  Sabel, BA  Reiser, G 
Citation: Rohatgi T, etal., J Neurosci Res 2003 Jul 15;73(2):246-54.
RGD ID: 1299297
Pubmed: PMID:12836167   (View Abstract at PubMed)
DOI: DOI:10.1002/jnr.10643   (Journal Full-text)

Protease-activated receptors (PARs), 7-transmembrane domain G protein-coupled receptors, are involved in tissue degeneration and repair upon injury. We demonstrate the expression of all four PAR subtypes in the postnatal eye and in retina of the adult rat by reverse transcription-polymerase chain reaction (RT-PCR). PAR-1 is regulated developmentally in the eye, with a decrease from P1, P9, to P16, whereas levels for PAR-2, PAR-3, and PAR-4 remain unchanged throughout. In the retina of the adult rat, PAR-1 is highly expressed, whereas PAR-2 and PAR-3 are moderately expressed, compared to low PAR-4 expression. To elucidate possible roles of PARs after trauma, we carried out semiquantitative RT-PCR analysis of expression of all 4 PAR subtypes, beginning 6 hr after partial optic nerve crush (ONC) in the adult rat until 3 weeks after the mild trauma. Levels of PAR mRNA for all four subtypes were upregulated as early as 6 hr after unilateral ONC, except PAR-3, which showed a delayed upregulation. PAR-1, PAR-3, and PAR-4 mRNA levels returned to almost basal levels at 3 weeks post-crush, whereas PAR-2 mRNA level was still high by the end of 3 weeks after crush. Although the lesion was unilateral, PAR mRNA expression in the contralateral, uninjured side was affected to levels almost comparable to those in the injured side. Previous studies have shown an increase in thrombin levels at the site of injury, retinal ganglion cell degeneration by necrosis and apoptosis, and PAR activation as consequences of nerve crush. PAR upregulation because of nerve crush in the mild trauma model could act as an effector of early cell death. Eventual return of receptor mRNA to basal levels is consistent with neuroprotection.

RGD Manual Disease Annotations    Click to see Annotation Detail View
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
Optic Nerve Injuries  ISOPawr (Rattus norvegicus)1299297; 1299297mRNA:increased expression:retina:RGD 
Optic Nerve Injuries  IEP 1299297mRNA:increased expression:retina:RGD 

Gene Ontology Annotations    Click to see Annotation Detail View

Molecular Function
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
G protein-coupled receptor activity  TAS 1299297 RGD 

Objects Annotated

Genes (Rattus norvegicus)
F2rl2  (coagulation factor II (thrombin) receptor-like 2)
Pawr  (pro-apoptotic WT1 regulator)

Genes (Mus musculus)
Pawr  (PRKC, apoptosis, WT1, regulator)

Genes (Homo sapiens)
PAWR  (pro-apoptotic WT1 regulator)

Objects referenced in this article
Gene F2r coagulation factor II (thrombin) receptor Rattus norvegicus
Gene F2rl1 F2R like trypsin receptor 1 Rattus norvegicus

Additional Information