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Monocytes are key regulators of innate immunity and play a critical role in the renewal of the peripheral mononuclear phagocytic system and in case of inflammation. This manuscript describes the procedure of real time imaging of the mouse calvaria bone marrow to study the monocyte mobilisation mechanism.
Real time multiphoton imaging provides a great opportunity to study cell trafficking and cell-to-cell interactions in their physiological 3-dimensionnal environment. Biological activities of immune cells mainly rely on their motility capacities. Blood monocytes have short half-life in the bloodstream; they originate in the bone marrow and are constitutively released from it. In inflammatory condition, this process is enhanced, leading to blood monocytosis and subsequent infiltration of the peripheral inflammatory tissues. Identifying the biomechanical events controlling monocyte trafficking from the bone marrow towards the vascular network is an important step to understand monocyte physiopathological relevance. We performed in vivo time-lapse imaging by two-photon microscopy of the skull bone marrow of the Csf1r-Gal4VP16/UAS-ECFP (MacBlue) mouse. The MacBlue mouse expresses the fluorescent reporters enhanced cyan fluorescent protein (ECFP) under the control of a myeloid specific promoter 1, in combination with vascular network labelling. We describe how this approach enables the tracking of individual medullar monocytes in real time to further quantify the migratory behaviour within the bone marrow parenchyma and the vasculature, as well as cell-to-cell interactions. This approach provides novel insights into the biology of the bone marrow monocyte subsets and allows to further address how these cells can be influenced in specific pathological conditions.
The bone marrow plays a central role in hematopoiesis and represents the main reservoir of monocytes that constitutively recirculate between the blood and the medullar parenchyma, renew the pool of circulating monocytes with a short life span 2,3 and participate in the reconstitution of the steady state tissue-macrophages and dendritic cells 4. During inflammation or after transient aplasia, monocytes are actively mobilized from either the bone marrow or the spleen 5, 6, 7 and colonize inflamed organs. Several chemoattractant axis have been involved in the process of myeloid cell mobilization from the bone marrow 8, 5, ....
NOTE: All experiment protocols were approved by the French Animal Experimentation and Ethics Committee and validated by the “Service Protection et Santé Animales, Environnement” with number A-75-2065. Sample sizes are chosen to ensure reproducibility of the experiments, and according to the 3R of animal ethic regulation.
1. Preparation of the Mouse
Mouse skull structure offers a good opportunity to study the bone marrow physiology by intravital imaging. The bone being thin around the front-parietal area, it is possible to get access to medullar niches without abrasion of the bone. Figure 1 represents a wide 2D field of the skull of a MacBlue transgenic mouse. The bone matrix is mainly composed of collagen I easily detectable by SHG 19. Injection of rhodamin-dextran stains the vascular network of the bone marrow and allows for the identif.......
The critical points of in vivo imaging methodology are to ensure stability of the focus in order to maximize the duration of imaging and to minimize the risk of bacterial contamination and inflammation, which might impact the dynamics of the inflammatory cells. Imaging of the skull bone marrow follows these aims as the surgery performed to get access to the bone marrow is minimal. The use of sterile material and antiseptics is essential to limit the risk of infection that might induce perturbation in cel.......
The authors have nothing to disclose.
The authors wish to thank Anne Daron and Pierre Louis Loyher for editorial assistance, the Plateforme Imagerie Pitié-Salpêtrière (PICPS) for assistance with the two-photon microscope and the animal Facility “NAC” and Camille Baudesson for mice breeding assistance. The research leading to these results has received funding from the European Community’s Seventh Framework Programme (FP7/2007-2013) under grant agreement n° 304810 – RAIDs, and n°241440-Endostem, from Inserm, from Université Pierre et Marie Curie “Emergence”, from la “Ligue contre le cancer”, from “Association pour la Recher....
Name | Company | Catalog Number | Comments |
Name of Material/ Equipment | Company | Catalog Number | Comments/Description |
Ketamin | Merial | 100mg/mL, anesthetic | |
Xylazin | Bayer HealthCare | 10mg/mL, anesthetic | |
Isofluran | Baxter | 2.5%, anesthetic | |
O2/NO2 | 70/30 mixture, anesthetic | ||
Rhodamin-Dextran | Invitrogen | 2MDa, 10mg/mL, Vascular staining | |
Ly6G-PE | Becton-Dickinson | clone 1A8, neutrophils staining | |
Stereotactic holder | Home made | surgery | |
Ethanol 70% | surgery | ||
Sterile scissors and nippers | surgery | ||
Rubber ring | 18mm diameter, surgery | ||
Glubran 2 | Queryo Medical | Surgical Glue, rubber ring fixation | |
Small gauge needles | Terumo | surgery | |
Zeiss LSM 710 NLO multiphoton microscope | Carl Zeiss | Microscope | |
Ti:Sapphire crystal laser | Coherent Chameleon Ultra | 140fs pulses of NIR light | |
Zen 2010 | Carl Zeiss | Acquistion Software | |
Imaris Bitplane | Bitplane | Analysis Software, 3D automatic tracking | |
PBS 1X | D. Dutscher | surgery | |
Thermostated chamber | Carl Zeiss | intravital imaging |
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