Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brain

Summary: Stem cell therapy shows promise for multiple disorders; however, the molecular crosstalk between grafted cells and host tissue is largely unknown. Here, we take a step toward addressing this question. Using translating ribosome affinity purification (TRAP) with sequencing tools, we simultan...

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Main Authors: Ricardo L. Azevedo-Pereira, Nathan C. Manley, Chen Dong, Yue Zhang, Alex G. Lee, Yulia Zatulovskaia, Varun Gupta, Jennifer Vu, Summer Han, Jack E. Berry, Tonya M. Bliss, Gary K. Steinberg
Format: Article
Language:English
Published: Elsevier 2023-04-01
Series:Cell Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124723003649
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author Ricardo L. Azevedo-Pereira
Nathan C. Manley
Chen Dong
Yue Zhang
Alex G. Lee
Yulia Zatulovskaia
Varun Gupta
Jennifer Vu
Summer Han
Jack E. Berry
Tonya M. Bliss
Gary K. Steinberg
author_facet Ricardo L. Azevedo-Pereira
Nathan C. Manley
Chen Dong
Yue Zhang
Alex G. Lee
Yulia Zatulovskaia
Varun Gupta
Jennifer Vu
Summer Han
Jack E. Berry
Tonya M. Bliss
Gary K. Steinberg
author_sort Ricardo L. Azevedo-Pereira
collection DOAJ
description Summary: Stem cell therapy shows promise for multiple disorders; however, the molecular crosstalk between grafted cells and host tissue is largely unknown. Here, we take a step toward addressing this question. Using translating ribosome affinity purification (TRAP) with sequencing tools, we simultaneously decode the transcriptomes of graft and host for human neural stem cells (hNSCs) transplanted into the stroke-injured rat brain. Employing pathway analysis tools, we investigate the interactions between the two transcriptomes to predict molecular pathways linking host and graft genes; as proof of concept, we predict host-secreted factors that signal to the graft and the downstream molecular cascades they trigger in the graft. We identify a potential host-graft crosstalk pathway where BMP6 from the stroke-injured brain induces graft secretion of noggin, a known brain repair factor. Decoding the molecular interplay between graft and host is a critical step toward deciphering the molecular mechanisms of stem cell action.
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spelling doaj.art-60fffa56c0664d14a22e17445291e7522023-04-12T04:11:42ZengElsevierCell Reports2211-12472023-04-01424112353Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brainRicardo L. Azevedo-Pereira0Nathan C. Manley1Chen Dong2Yue Zhang3Alex G. Lee4Yulia Zatulovskaia5Varun Gupta6Jennifer Vu7Summer Han8Jack E. Berry9Tonya M. Bliss10Gary K. Steinberg11Department of Neurosurgery, Stanford University, Stanford, CA 94305, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USAStanford Genetics Bioinformatics Service Center, Stanford University, Stanford, CA 94305, USADivision of Hematology and Oncology, Department of Pediatrics, University of California, San Francisco, CA 94143, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USADepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USA; Corresponding authorDepartment of Neurosurgery, Stanford University, Stanford, CA 94305, USA; Corresponding authorSummary: Stem cell therapy shows promise for multiple disorders; however, the molecular crosstalk between grafted cells and host tissue is largely unknown. Here, we take a step toward addressing this question. Using translating ribosome affinity purification (TRAP) with sequencing tools, we simultaneously decode the transcriptomes of graft and host for human neural stem cells (hNSCs) transplanted into the stroke-injured rat brain. Employing pathway analysis tools, we investigate the interactions between the two transcriptomes to predict molecular pathways linking host and graft genes; as proof of concept, we predict host-secreted factors that signal to the graft and the downstream molecular cascades they trigger in the graft. We identify a potential host-graft crosstalk pathway where BMP6 from the stroke-injured brain induces graft secretion of noggin, a known brain repair factor. Decoding the molecular interplay between graft and host is a critical step toward deciphering the molecular mechanisms of stem cell action.http://www.sciencedirect.com/science/article/pii/S2211124723003649CP: NeuroscienceCP: Stem cell research
spellingShingle Ricardo L. Azevedo-Pereira
Nathan C. Manley
Chen Dong
Yue Zhang
Alex G. Lee
Yulia Zatulovskaia
Varun Gupta
Jennifer Vu
Summer Han
Jack E. Berry
Tonya M. Bliss
Gary K. Steinberg
Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brain
Cell Reports
CP: Neuroscience
CP: Stem cell research
title Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brain
title_full Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brain
title_fullStr Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brain
title_full_unstemmed Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brain
title_short Decoding the molecular crosstalk between grafted stem cells and the stroke-injured brain
title_sort decoding the molecular crosstalk between grafted stem cells and the stroke injured brain
topic CP: Neuroscience
CP: Stem cell research
url http://www.sciencedirect.com/science/article/pii/S2211124723003649
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