PMID- 35295714 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20221004 IS - 2329-423X (Print) IS - 2329-4248 (Electronic) IS - 2329-423X (Linking) VI - 9 IP - 2 DP - 2022 Apr TI - Toolbox for studying neurovascular coupling in vivo, with a focus on vascular activity and calcium dynamics in astrocytes. PG - 021909 LID - 10.1117/1.NPh.9.2.021909 [doi] LID - 021909 AB - Significance: Insights into the cellular activity of each member of the neurovascular unit (NVU) is critical for understanding their contributions to neurovascular coupling (NVC)-one of the key control mechanisms in cerebral blood flow regulation. Advances in imaging and genetic tools have enhanced our ability to observe, manipulate and understand the cellular activity of NVU components, namely neurons, astrocytes, microglia, endothelial cells, vascular smooth muscle cells, and pericytes. However, there are still many unresolved questions. Since astrocytes are considered electrically unexcitable, Ca2+ signaling is the main parameter used to monitor their activity. It is therefore imperative to study astrocytic Ca2+ dynamics simultaneously with vascular activity using tools appropriate for the question of interest. Aim: To highlight currently available genetic and imaging tools for studying the NVU-and thus NVC-with a focus on astrocyte Ca2+ dynamics and vascular activity, and discuss the utility, technical advantages, and limitations of these tools for elucidating NVC mechanisms. Approach: We draw attention to some outstanding questions regarding the mechanistic basis of NVC and emphasize the role of astrocytic Ca2+ elevations in functional hyperemia. We further discuss commonly used genetic, and optical imaging tools, as well as some newly developed imaging modalities for studying NVC at the cellular level, highlighting their advantages and limitations. Results: We provide an overview of the current state of NVC research, focusing on the role of astrocytic Ca2+ elevations in functional hyperemia; summarize recent advances in genetically engineered Ca2+ indicators, fluorescence microscopy techniques for studying NVC; and discuss the unmet challenges for future imaging development. Conclusions: Advances in imaging techniques together with improvements in genetic tools have significantly contributed to our understanding of NVC. Many pieces of the puzzle have been revealed, but many more remain to be discovered. Ultimately, optimizing NVC research will require a concerted effort to improve imaging techniques, available genetic tools, and analytical software. CI - (c) 2022 The Authors. FAU - Tran, Cam Ha T AU - Tran CHT AUID- ORCID: 0000-0003-1177-7723 AD - University of Nevada, Reno School of Medicine, Department of Physiology and Cell Biology, Reno, Nevada, United States. LA - eng GR - P20 GM130459/GM/NIGMS NIH HHS/United States GR - R01 NS121543/NS/NINDS NIH HHS/United States GR - R21 AG073780/AG/NIA NIH HHS/United States PT - Journal Article PT - Review DEP - 20220314 PL - United States TA - Neurophotonics JT - Neurophotonics JID - 101632875 PMC - PMC8920490 OTO - NOTNLM OT - astrocytes OT - calcium OT - endothelial cells OT - neurons OT - optogenetics OT - pericytes OT - three-dimensional volume imaging OT - two-photon imaging OT - vascular smooth muscle cells EDAT- 2022/03/18 06:00 MHDA- 2022/03/18 06:01 PMCR- 2022/03/14 CRDT- 2022/03/17 05:12 PHST- 2021/10/30 00:00 [received] PHST- 2022/02/23 00:00 [accepted] PHST- 2022/03/17 05:12 [entrez] PHST- 2022/03/18 06:00 [pubmed] PHST- 2022/03/18 06:01 [medline] PHST- 2022/03/14 00:00 [pmc-release] AID - 21059SSVR [pii] AID - 10.1117/1.NPh.9.2.021909 [doi] PST - ppublish SO - Neurophotonics. 2022 Apr;9(2):021909. doi: 10.1117/1.NPh.9.2.021909. Epub 2022 Mar 14.