Localization of sulfated glycoprotein-2/clusterin mRNA in the rat brain by in situ hybridization
- PMID: 8366194
- DOI: 10.1002/cne.903340205
Localization of sulfated glycoprotein-2/clusterin mRNA in the rat brain by in situ hybridization
Abstract
Sulfated glycoprotein-2 (SGP-2) gene expression seems to be constitutively expressed in a variety of tissues and organs, although levels of expression vary widely from one tissue to the other. SGP-2, also known as clusterin, has been reported to be expressed in the central nervous system (CNS). Some possible roles for brain SGP-2 have been postulated. In order to provide a substrate for a better understanding of the functions of this glycoprotein in the CNS, we investigated the detailed anatomical and cellular distribution of SGP-2 mRNA in the adult rat brain as well as the variation in its cellular expression after excitotoxin lesion. Transcripts for SGP-2 were found to be distributed throughout the rat CNS, although regional differences in their prevalence were readily observed. The ependymal lining of the ventricles showed the highest level of expression followed by various gray matter areas, some of which contained very intensively labeled cells. These cells were mostly found among several hypothalamic and brainstem nuclei, the habenular complex, as well as in the ventral horn of the spinal cord, which displayed striking hybridization signals over motoneurons. Occasional cells expressing high levels of SGP-2 transcripts were found in fiber tracts. Highly SGP-2 mRNA-positive resting glial cells were mainly located near the glial limitans and blood vessels. Two areas of relatively low constitutive SGP-2 mRNA expression are shown to produce strong hybridization signals 10 days after the local administration of the excitotoxin kainic acid. This overexpression of SGP-2 transcripts appears to involve GFAP-positive cells. Taken together, these results indicate that in the intact adult rat CNS, various cell populations, including neurons, constitutively express SGP-2 transcripts, whereas in the injured brain, reactive astrocytes become the major producers.
Similar articles
-
Lack of correspondence between mRNA expression for a putative cell death molecule (SGP-2) and neuronal cell death in the central nervous system.J Neurobiol. 1991 Sep;22(6):590-604. doi: 10.1002/neu.480220605. J Neurobiol. 1991. PMID: 1919566
-
Clusterin (SGP-2): a multifunctional glycoprotein with regional expression in astrocytes and neurons of the adult rat brain.J Comp Neurol. 1994 Jan 15;339(3):387-400. doi: 10.1002/cne.903390307. J Comp Neurol. 1994. PMID: 8132868
-
Follicular atresia as an apoptotic process: atresia-associated increase in the ovarian expression of the putative apoptotic marker sulfated glycoprotein-2.J Soc Gynecol Investig. 1996 Jul-Aug;3(4):199-208. J Soc Gynecol Investig. 1996. PMID: 8796831
-
Possible functions of a new genetic marker in central nervous system: the sulfated glycoprotein-2 (SGP-2).Synapse. 1992 Jun;11(2):105-11. doi: 10.1002/syn.890110203. Synapse. 1992. PMID: 1626310 Review.
-
Sulfated glycoprotein 2: new relationships of this multifunctional protein to neurodegeneration.Trends Neurosci. 1992 Oct;15(10):391-6. doi: 10.1016/0166-2236(92)90190-j. Trends Neurosci. 1992. PMID: 1279864 Review.
Cited by
-
Stress-induced transcription of the clusterin/apoJ gene.Biochem J. 1997 Nov 15;328 ( Pt 1)(Pt 1):45-50. doi: 10.1042/bj3280045. Biochem J. 1997. PMID: 9359832 Free PMC article.
-
Clusterin and LRP2 are critical components of the hypothalamic feeding regulatory pathway.Nat Commun. 2013;4:1862. doi: 10.1038/ncomms2896. Nat Commun. 2013. PMID: 23673647
-
Clusterin Expression in Colorectal Carcinomas.Int J Mol Sci. 2023 Sep 27;24(19):14641. doi: 10.3390/ijms241914641. Int J Mol Sci. 2023. PMID: 37834086 Free PMC article. Review.
-
Association between clusterin polymorphisms and esophageal squamous cell carcinoma risk in Han Chinese population.Int J Clin Exp Med. 2015 Aug 15;8(8):14004-10. eCollection 2015. Int J Clin Exp Med. 2015. PMID: 26550359 Free PMC article.
-
Glial activation and inflammation along the Alzheimer's disease continuum.J Neuroinflammation. 2019 Feb 21;16(1):46. doi: 10.1186/s12974-019-1399-2. J Neuroinflammation. 2019. PMID: 30791945 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous