Jun Yin, Hsueh-Ling Chen, Anna Grigsby-Brown, Yi He, Myriam L. Cotten, Jacob Short, Aidan Dermady, Jingce Lei, Mary Gibbs, Ethan S. Cheng, Dean Zhang, Caixia Long, Jennifer Tabet, Lele Xu, Tiffany Zhong, Rinat Abzalimov, Mariam Haider, Rong Sun, Ye He, Qiangjun Zhou, Nico Tjandra, Quan Yuan
{"title":"胶质细胞衍生的非典型脂肪酸结合蛋白调节脑脂质储存和清除","authors":"Jun Yin, Hsueh-Ling Chen, Anna Grigsby-Brown, Yi He, Myriam L. Cotten, Jacob Short, Aidan Dermady, Jingce Lei, Mary Gibbs, Ethan S. Cheng, Dean Zhang, Caixia Long, Jennifer Tabet, Lele Xu, Tiffany Zhong, Rinat Abzalimov, Mariam Haider, Rong Sun, Ye He, Qiangjun Zhou, Nico Tjandra, Quan Yuan","doi":"10.1126/sciadv.adv2902","DOIUrl":null,"url":null,"abstract":"<div >Glia-derived secretory factors are essential for brain development, physiology, and homeostasis, with their dysfunction linked to a variety of neurological disorders. Through genetic and biochemical approaches, we identified odorant binding protein 44a (Obp44a), a noncanonical α-helical fatty acid binding protein (FABP) highly expressed in <i>Drosophila</i> central nervous system glia. Obp44a binds long-chain fatty acids and shuttles between glia and neurons, acting as a secretory lipid chaperone and scavenger to support lipid storage, efflux, and redox homeostasis. Notably, Obp44a is recruited to apoptotic cells and injured axons, especially when glial engulfment is impaired, demonstrating its role in lipid waste management and clearance of cellular debris during development and in pathological states. Our findings highlight FABPs’ importance in regulating brain lipid dynamics and neuronal response to stress and injury. By visualizing FABP function in vivo, this study provides insights into how defective lipid regulation may contribute to neuronal stress and disease progression.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 31","pages":""},"PeriodicalIF":12.5000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.adv2902","citationCount":"0","resultStr":"{\"title\":\"Glia-derived noncanonical fatty acid binding protein modulates brain lipid storage and clearance\",\"authors\":\"Jun Yin, Hsueh-Ling Chen, Anna Grigsby-Brown, Yi He, Myriam L. Cotten, Jacob Short, Aidan Dermady, Jingce Lei, Mary Gibbs, Ethan S. Cheng, Dean Zhang, Caixia Long, Jennifer Tabet, Lele Xu, Tiffany Zhong, Rinat Abzalimov, Mariam Haider, Rong Sun, Ye He, Qiangjun Zhou, Nico Tjandra, Quan Yuan\",\"doi\":\"10.1126/sciadv.adv2902\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div >Glia-derived secretory factors are essential for brain development, physiology, and homeostasis, with their dysfunction linked to a variety of neurological disorders. Through genetic and biochemical approaches, we identified odorant binding protein 44a (Obp44a), a noncanonical α-helical fatty acid binding protein (FABP) highly expressed in <i>Drosophila</i> central nervous system glia. Obp44a binds long-chain fatty acids and shuttles between glia and neurons, acting as a secretory lipid chaperone and scavenger to support lipid storage, efflux, and redox homeostasis. Notably, Obp44a is recruited to apoptotic cells and injured axons, especially when glial engulfment is impaired, demonstrating its role in lipid waste management and clearance of cellular debris during development and in pathological states. Our findings highlight FABPs’ importance in regulating brain lipid dynamics and neuronal response to stress and injury. By visualizing FABP function in vivo, this study provides insights into how defective lipid regulation may contribute to neuronal stress and disease progression.</div>\",\"PeriodicalId\":21609,\"journal\":{\"name\":\"Science Advances\",\"volume\":\"11 31\",\"pages\":\"\"},\"PeriodicalIF\":12.5000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.science.org/doi/reader/10.1126/sciadv.adv2902\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science Advances\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.science.org/doi/10.1126/sciadv.adv2902\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adv2902","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Glia-derived noncanonical fatty acid binding protein modulates brain lipid storage and clearance
Glia-derived secretory factors are essential for brain development, physiology, and homeostasis, with their dysfunction linked to a variety of neurological disorders. Through genetic and biochemical approaches, we identified odorant binding protein 44a (Obp44a), a noncanonical α-helical fatty acid binding protein (FABP) highly expressed in Drosophila central nervous system glia. Obp44a binds long-chain fatty acids and shuttles between glia and neurons, acting as a secretory lipid chaperone and scavenger to support lipid storage, efflux, and redox homeostasis. Notably, Obp44a is recruited to apoptotic cells and injured axons, especially when glial engulfment is impaired, demonstrating its role in lipid waste management and clearance of cellular debris during development and in pathological states. Our findings highlight FABPs’ importance in regulating brain lipid dynamics and neuronal response to stress and injury. By visualizing FABP function in vivo, this study provides insights into how defective lipid regulation may contribute to neuronal stress and disease progression.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.