Cadherin‐6 is a novel mediator for the migration of mesenchymal stem cells to glioblastoma cells in response to stromal cell‐derived factor‐1

Author:

Park Aran1,Kim Seung‐Eun2,Yu Jinyeong3,Son Donghyun2,Kim Kyung‐Sup4,Koh Eunjin4,Park Ki‐Sook25ORCID

Affiliation:

1. Graduate School of Biotechnology Kyung Hee University Yongin Korea

2. Department of Biomedical Science and Technology, Graduate School Kyung Hee University Seoul Korea

3. Industry‐Academic Cooperation Foundation Kyung Hee University Seoul Korea

4. Department of Biochemistry and Molecular Biology, College of Medicine Yonsei University Seoul Korea

5. East‐West Medical Research Institute Kyung Hee University Seoul Korea

Abstract

Glioblastoma recruits various nontransformed cells from distant tissues. Although bone marrow‐derived mesenchymal stem cells (MSCs) have been observed migrating to glioblastoma, the underlying mechanism driving MSC migration toward glioblastoma remains unclear. Tumor vascularity is critical in the context of recurrent glioblastoma and is closely linked to the expression of stromal cell‐derived factor‐1 (SDF‐1). We demonstrated that cadherin‐6 mediated MSC migration both toward SDF‐1 and toward glioblastoma cells. Cadherin‐6 knockdown resulted in the downregulation of MSCs capacity to migrate in response to SDF‐1. Furthermore, MSCs with cadherin‐6 knockdown exhibited impaired migration in response to conditioned media derived from glioblastoma cell lines (U87 and U373) expressing SDF‐1, thus simulating the glioblastoma microenvironment. Moreover, MSCs enhanced the vasculogenic capacity of U87 cells without increasing the proliferation, cancer stem cell characteristics, or migration of U87. These results suggest that the current strategy of utilizing MSCs as carriers for antiglioblastoma drugs requires careful examination. Furthermore, cadherin‐6 may represent a novel potential target for controlling the recruitment of MSCs toward glioblastoma.

Funder

Neurosciences Research Foundation

Publisher

Wiley

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