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Geisness, Athena

https://orcid.org/0009-0008-9147-2631

Mayo Clinic

University of Minnesota

Citations 1

An irradiated marrow niche reveals a small non-collagenous protein mediator of homing, dermatopontin
Kramer, Ashley C. , Astuti, Yuliana, Elfstrum, Alexis K. , Lehrke, Michael Jonathan , Tolar, Jakub , Blazar, Bruce R. , Blake, Amanda L., Taisto, Mandy, Furcich, Justin W. , Nolan, Erin E. , Webber, Beau R. , Geisness, Athena , Lehrke, Michael J , Durose, Wilaiwan W , Webber, Beau R , Blazar, Bruce R , Tolar, Jakub , Wood, David K. , Lund, Troy C.

Blood Advances | August 27, 2021 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.1182/bloodadvances.2021004475 Get It

Hematopoietic cell homing after hematopoietic cell transplant (HCT) is governed by several pathways involving marrow niche cells that are evoked after pre-HCT conditioning. To understand the factors that play a role in homing, we performed expression analysis on the zebrafish marrow niche cells following conditioning. We determined that the non-collagenous protein extracellular matrix related protein dermatopontin (Dpt) was upregulated seven-fold in response to irradiation. Studies in mice revealed DPT induction both with radiation and lipopolysaccharide exposure. Interestingly, we found that co-incubation of zebrafish or murine hematopoietic cells with rDPT impedes hematopoietic stem and progenitor cell homing by 50% and 86%, respectively. Similarly, this translated into a 24% reduction in long term engraftment (versus control, p = 0.01). We found DPT to interact with VLA-4 and block hematopoietic - endothelial cell adhesion and transendothelial migration. Finally, a DPT knockout mouse displayed a 60% increase in homing of hematopoietic cells versus wildtype (p = 0.03) with slight improvement in long-term LSK-SLAM engraftment (2-fold, p = 0.04). These data show that the extracellular matrix (ECM)-related protein DPT increases with radiation and transiently impedes the transendothelial migration of hematopoietic cells to the marrow.