<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>287(12)</volume><submitter>Lee S</submitter><pubmed_abstract>Prostaglandin D synthase (PGDS) is responsible for the conversion of PGH(2) to PGD(2). Two distinct types of PGDS have been identified: hematopoietic-type PGDS (H-PGDS) and lipocalin-type PGDS (L-PGDS). L-PGDS acts as both a PGD(2)-synthesizing enzyme and as an extracellular transporter of various lipophilic small molecules. Although L-PGDS is one of the most abundant proteins in the cerebrospinal fluid, little is known about the function of L-PGDS in the central nervous system (CNS). To better understand the role of L-PGDS in the CNS, effects of L-PGDS on the migration and morphology of glial cells were investigated. The L-PGDS protein accelerated the migration of cultured glial cells. Expression of the L-pgds gene was detected in glial cells and neurons. L-PGDS protein also induced morph</pubmed_abstract><journal>The Journal of biological chemistry</journal><pagination>9414-28</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3308805</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lipocalin-type prostaglandin D2 synthase protein regulates glial cell migration and morphology through myristoylated alanine-rich C-kinase substrate: prostaglandin D2-independent effects.</pubmed_title><pmcid>PMC3308805</pmcid><pubmed_authors>Lee S</pubmed_authors><pubmed_authors>Jang E</pubmed_authors><pubmed_authors>Kim JH</pubmed_authors><pubmed_authors>Lee WH</pubmed_authors><pubmed_authors>Suk K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lipocalin-type prostaglandin D2 synthase protein regulates glial cell migration and morphology through myristoylated alanine-rich C-kinase substrate: prostaglandin D2-independent effects.</name><description>Prostaglandin D synthase (PGDS) is responsible for the conversion of PGH(2) to PGD(2). Two distinct types of PGDS have been identified: hematopoietic-type PGDS (H-PGDS) and lipocalin-type PGDS (L-PGDS). L-PGDS acts as both a PGD(2)-synthesizing enzyme and as an extracellular transporter of various lipophilic small molecules. Although L-PGDS is one of the most abundant proteins in the cerebrospinal fluid, little is known about the function of L-PGDS in the central nervous system (CNS). To better understand the role of L-PGDS in the CNS, effects of L-PGDS on the migration and morphology of glial cells were investigated. The L-PGDS protein accelerated the migration of cultured glial cells. Expression of the L-pgds gene was detected in glial cells and neurons. L-PGDS protein also induced morph</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Mar</publication><modification>2025-04-05T12:06:53.758Z</modification><creation>2019-03-27T00:51:25Z</creation></dates><accession>S-EPMC3308805</accession><cross_references><pubmed>22275363</pubmed><doi>10.1074/jbc.m111.330662</doi><doi>10.1074/jbc.M111.330662</doi></cross_references></HashMap>