Hoyun Kwak , Eun-Ho Cho , Eun Bee Cho , Yoo-Na Lee , Anu Shahapal , Hyo Jeong Yong , Arfaxad Reyes-Alcaraz , Yongwoo Jeong , Yerim Lee , Minhyeok Lee , Nui Ha , Sitaek Oh , Jae Keun Lee , Won Suk Lee , Won Kyum Kim , Sangjin Yoo , Soon-Gu Kwon , Jong-Ik Hwang , Jae Young Seong
{"title":"Is FAM19A5 an adipokine? Peripheral FAM19A5 in wild-type, FAM19A5 knockout, and LacZ knockin mice","authors":"Hoyun Kwak , Eun-Ho Cho , Eun Bee Cho , Yoo-Na Lee , Anu Shahapal , Hyo Jeong Yong , Arfaxad Reyes-Alcaraz , Yongwoo Jeong , Yerim Lee , Minhyeok Lee , Nui Ha , Sitaek Oh , Jae Keun Lee , Won Suk Lee , Won Kyum Kim , Sangjin Yoo , Soon-Gu Kwon , Jong-Ik Hwang , Jae Young Seong","doi":"10.1016/j.mocell.2024.100125","DOIUrl":null,"url":null,"abstract":"<div><div><em>FAM19A5</em> is a novel secretory protein expressed primarily in the brain. However, a recent study reported that <em>FAM19A5</em> is an adipocyte-derived adipokine that regulates vascular smooth muscle function through sphingosine-1-phosphate receptor 2 (S1PR2). In our study, we investigated <em>FAM19A5</em> transcript and protein levels in peripheral tissues, including adipose tissues, from wild-type, <em>FAM19A5</em> knockout, and <em>FAM19A5</em>-<em>LacZ</em> knockin mice. We found that the <em>FAM19A5</em> transcript levels in the central nervous system were much greater than those in any of the peripheral tissues, including adipose tissues. Furthermore, the <em>FAM19A5</em> protein levels in adipose and reproductive tissues were below detectable limits for Western blot analysis and enzyme-linked immunosorbent assay (ELISA). Additionally, we found that the <em>FAM19A5</em> protein did not interact with S1PR2 in terms of G-protein-mediated signal transduction, β-arrestin recruitment, or ligand-mediated internalization. Taken together, our findings revealed basal levels of <em>FAM19A5</em> transcripts and proteins in peripheral tissues, confirming its primary expression in the central nervous system and lack of significant interaction with S1PR2.</div></div>","PeriodicalId":18795,"journal":{"name":"Molecules and Cells","volume":"47 12","pages":"Article 100125"},"PeriodicalIF":3.7000,"publicationDate":"2024-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecules and Cells","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S101684782400150X","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
FAM19A5 is a novel secretory protein expressed primarily in the brain. However, a recent study reported that FAM19A5 is an adipocyte-derived adipokine that regulates vascular smooth muscle function through sphingosine-1-phosphate receptor 2 (S1PR2). In our study, we investigated FAM19A5 transcript and protein levels in peripheral tissues, including adipose tissues, from wild-type, FAM19A5 knockout, and FAM19A5-LacZ knockin mice. We found that the FAM19A5 transcript levels in the central nervous system were much greater than those in any of the peripheral tissues, including adipose tissues. Furthermore, the FAM19A5 protein levels in adipose and reproductive tissues were below detectable limits for Western blot analysis and enzyme-linked immunosorbent assay (ELISA). Additionally, we found that the FAM19A5 protein did not interact with S1PR2 in terms of G-protein-mediated signal transduction, β-arrestin recruitment, or ligand-mediated internalization. Taken together, our findings revealed basal levels of FAM19A5 transcripts and proteins in peripheral tissues, confirming its primary expression in the central nervous system and lack of significant interaction with S1PR2.
期刊介绍:
Molecules and Cells is an international on-line open-access journal devoted to the advancement and dissemination of fundamental knowledge in molecular and cellular biology. It was launched in 1990 and ISO abbreviation is "Mol. Cells". Reports on a broad range of topics of general interest to molecular and cell biologists are published. It is published on the last day of each month by the Korean Society for Molecular and Cellular Biology.