Concentration and proteolysis of CX3CL1 may regulate the microglial response to CX3CL1-Reference-Cited by-同舟云学术

Concentration and proteolysis of CX3CL1 may regulate the microglial response to CX3CL1

Published:2022-09-15 Issue:2 Volume:71 Page:245-258
ISSN:0894-1491
Container-title:Glia
language:en
Short-container-title:Glia

Author:

Finneran Dylan¹²^ORCID,Li Qingyou¹,Subbarayan Meena S.¹³⁴,Joly‐Amado Aurelie¹,Kamath Siddharth¹,Dengler Daniela G.⁵,Gordon Marcia N.²,Jackson Michael R.⁵,Morgan Dave²,Bickford Paula C.¹³⁶,Smith Layton H.⁵,Nash Kevin R.¹^ORCID

Affiliation:

1. Department of Molecular Pharmacology and Physiology, Morsani College of Medicine University of South Florida Tampa USA

2. Department of Translational Neuroscience Michigan State University Grand Rapids Michigan USA

3. Center for Excellence in Aging and Brain Repair, Department of Neurosurgery and Brain Repair, Morsani College of Medicine University of South Florida Tampa USA

4. Gladstone Institute of Neurological Disease Gladstone Institutes San Francisco California USA

5. Conrad Prebys Center for Chemical Genomics, Sandford Burnham Prebys Medical Discovery Institute La Jolla California USA

6. Research Service James A Haley Veterans Hospital Tampa USA

Funder

National Institute on Aging

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/glia.24269

Reference57 articles.

1. A new class of membrane-bound chemokine with a CX3C motif

2. Genetically enhancing the expression of chemokine domain of CX3CL1 fails to prevent tau pathology in mouse models of tauopathy

3. Regulation of Tau Pathology by the Microglial Fractalkine Receptor

4. β-arrestin-Biased Agonism at the Parathyroid Hormone Receptor Uncouples Bone Formation from Bone Resorption

5. Control of microglial neurotoxicity by the fractalkine receptor

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