Aquaporin-4-dependent glymphatic solute transport in the rodent brain

Author:

Mestre Humberto1ORCID,Hablitz Lauren M1ORCID,Xavier Anna LR2,Feng Weixi3,Zou Wenyan3,Pu Tinglin3,Monai Hiromu45ORCID,Murlidharan Giridhar6,Castellanos Rivera Ruth M6,Simon Matthew J7,Pike Martin M8,Plá Virginia1ORCID,Du Ting1,Kress Benjamin T1,Wang Xiaowen4,Plog Benjamin A1,Thrane Alexander S29,Lundgaard Iben11011,Abe Yoichiro12ORCID,Yasui Masato12,Thomas John H1314,Xiao Ming3,Hirase Hajime415ORCID,Asokan Aravind61617,Iliff Jeffrey J718,Nedergaard Maiken12ORCID

Affiliation:

1. Center for Translational Neuromedicine, University of Rochester Medical Center, Rochester, United States

2. Center for Translational Neuromedicine, Faculty of Medical and Health Sciences, University of Copenhagen, Copenhagen, Denmark

3. Jiangsu Province Key Laboratory of Neurodegeneration, Center for Global Health, Nanjing Medical University, Nanjing, China

4. RIKEN Center for Brain Science, Wako, Japan

5. Ochanomizu University, Tokyo, Japan

6. Gene Therapy Center, The University of North Carolina, Chapel Hill, United States

7. Department of Anesthesiology and Perioperative Medicine, Oregon Health and Science University, Portland, United States

8. Advanced Imaging Research Center, Oregon Health and Science University, Portland, United States

9. Department of Ophthalmology, Haukeland University Hospital, Bergen, Norway

10. Department of Experimental Medical Science, Lund University, Lund, Sweden

11. Wallenberg Center for Molecular Medicine, Lund University, Lund, Sweden

12. Department of Pharmacology,School of Medicine, Keio University, Tokyo, Japan

13. Department of Mechanical Engineering, University of Rochester, Rochester, United States

14. Department of Physics and Astronomy, University of Rochester, Rochester, United States

15. Brain and Body System Science Institute, Saitama University, Saitama, Japan

16. Department of Molecular Genetics and Microbiology, Duke University School of Medicine, North Carolina, United States

17. Department of Surgery, Duke University School of Medicine, Durham, United States

18. Knight Cardiovascular Institute, Oregon Health and Science University, Portland, United States

Abstract

The glymphatic system is a brain-wide clearance pathway; its impairment contributes to the accumulation of amyloid-β. Influx of cerebrospinal fluid (CSF) depends upon the expression and perivascular localization of the astroglial water channel aquaporin-4 (AQP4). Prompted by a recent failure to find an effect of Aqp4 knock-out (KO) on CSF and interstitial fluid (ISF) tracer transport, five groups re-examined the importance of AQP4 in glymphatic transport. We concur that CSF influx is higher in wild-type mice than in four different Aqp4 KO lines and in one line that lacks perivascular AQP4 (Snta1 KO). Meta-analysis of all studies demonstrated a significant decrease in tracer transport in KO mice and rats compared to controls. Meta-regression indicated that anesthesia, age, and tracer delivery explain the opposing results. We also report that intrastriatal injections suppress glymphatic function. This validates the role of AQP4 and shows that glymphatic studies must avoid the use of invasive procedures.

Funder

Japan Society for the Promotion of Science

Knut och Alice Wallenbergs Stiftelse

National Institute on Aging

Human Frontier Science Program

Lundbeckfonden

National Institutes of Health

Dr. Miriam and Sheldon G. Adelson Medical Research Foundation

EU Joint Programme – Neurodegenerative Disease Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Reference73 articles.

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