Author:
Barrett Thomas F.,Patel Bhuvic,Khan Saad M.,Yim Aldrin K.Y.,Pugazenthi Sangami,Mahlokozera Tatenda,Mullins Riley D.Z.,Zipfel Gregory J.,Herzog Jacques A.,Chicoine Michael R.,Wick Cameron C.,Durakovic Nedim,Osbun Joshua W.,Shew Matthew,Sweeney Alex D.,Patel Akash J.,Buchman Craig A.,Petti Allegra A.,Puram Sidharth V.,Kim Albert H.
Abstract
ABSTRACTVestibular schwannomas (VS) are benign tumors that lead to significant neurologic and otologic morbidity. How VS heterogeneity and the tumor microenvironment (TME) contribute to the pathogenesis of these tumors remains poorly understood. We performed scRNA-seq on 15 VS samples, with paired scATAC-seq in six samples. We identified diverse Schwann cell (SC), stromal, and immune populations in the VS TME and found that repair-like and MHC-II antigen presenting subtype SCs are associated with increased myeloid cell infiltrate, implicating a nerve injury-like process. Deconvolution analysis of RNA-expression data from 175 tumors revealed Injury-like tumors are associated with larger tumor size, and scATAC-seq identified transcription factors associated with nerve repair among SCs from Injury-like tumors. Ligand-receptor analysis and functionalin vitroexperiments suggested that SCs recruit monocytes. Our study indicates that Injury-like SCs may cause tumor growth via myeloid cell recruitment and identifies molecular pathways that may be targeted to prevent tumor progression.
Publisher
Cold Spring Harbor Laboratory