The present protocol describes a mouse model of the ablation of adrenergic innervation by identifying and resecting the superior cervical ganglion.
A subscription to JoVE is required to view this content. Sign in or start your free trial.
Method Article
The present protocol describes a mouse model of the ablation of adrenergic innervation by identifying and resecting the superior cervical ganglion.
Growing evidence suggests that the sympathetic nervous system plays an important role in cancer progression. Adrenergic innervation regulates salivary gland secretion, circadian rhythm, macular degeneration, immune function, and cardiac physiology. Murine surgical sympathectomy is a method for studying the effects of adrenergic innervation by allowing for complete, unilateral adrenergic ablation while avoiding the need for repeated pharmacologic intervention and the associated side effects. However, surgical sympathectomy in mice is technically challenging because of the small size of the superior cervical ganglion. This study describes a surgical technique for reliably identifying and resecting the superior cervical ganglion to ablate the sympathetic nervous system. The successful identification and removal of the ganglion are validated by imaging the fluorescent sympathetic ganglia using a transgenic mouse, identifying post-resection Horner's syndrome, staining for adrenergic markers in the resected ganglia, and observing diminished adrenergic immunofluorescence in the target organs following sympathectomy. This model enables future studies of cancer progression as well as other physiological processes regulated by the sympathetic nervous system.
Multiple studies have reported that the nerves in the tumor microenvironment play an active role in supporting tumor progression. The ablation of adrenergic sympathetic nerves has been shown to impair tumor development and dissemination in prostate and gastric cancer in vivo1,2,3, while the pharmacological blockade of adrenergic receptors inhibits tumor growth in head and neck cancer4. Sympathetic neural involvement has also been described in pancreatic, cervical, and basal cell carcinoma progression5,
Access restricted. Please log in or start a trial to view this content.
The animal procedures described here were approved by the Institutional Animal Care and Use Committee at the Memorial Sloan Kettering Cancer Center. Eight-week-old male and female NSG mice were used here. The animals were obtained from a commercial source (see Table of Materials). The instruments are sterilized, the surgical working surface is disinfected, the animal's skin surface is disinfected, and the surgeon wears sterile gloves throughout the procedure.
1. Preparation of the mice and preoperative setup
Access restricted. Please log in or start a trial to view this content.
This protocol describes the surgical removal of the SCG in a mouse model. Figure 2 illustrates the anatomical landmarks, including the CCA, the anterior jugular vein, and the SCG. With dissection (Figure 2A), the right anterior jugular vein can be seen coursing alongside the lateral border of the trachea. As it is located deeper than the anterior jugular vein, the left CCA and its bifurcation into the internal carotid artery (ICA) and external carotid artery (EC.......
Access restricted. Please log in or start a trial to view this content.
This protocol describes a mouse model for the surgical unilateral ablation of SCG input. This technique allows for studying the effects of adrenergic innervation in various settings. In addition, the resected sympathetic ganglion can also be grown in 3D matrigel culture for in vitro experiments30.
Studies involving SCGx have mostly been performed in rats, as their larger anatomy allows for easier anatomic visualization and dissection. While SCGx in mice has bee.......
Access restricted. Please log in or start a trial to view this content.
The authors have nothing to disclose.
Q. W. was supported by NIH T32CA009685. R. J. W. was supported by NIH R01CA219534. The Memorial Sloan Kettering Cancer Center Core Facilities were supported by NIH P30CA008748.
....Access restricted. Please log in or start a trial to view this content.
| Name | Company | Catalog Number | Comments |
|---|---|---|---|
| Anti-Tyrosine Hydroxylase Antibody | EMD Millipore | AB152 | |
| Artificial Tears Lubricant Ophthalmic Ointment | Akorn | 59399-162-35 | |
| Curity 2 x 2 Inch Gauze Sponge 8 Ply, Sterile | Covidien | 1806 | |
| Derf Needle Holder | Thomas Scientific | 1177K00 | |
| Dissecting Microscope | |||
| Dumont #5/45 Forceps | Fine Science Tools | 11251-35 | |
| Dumont #7b Forceps | Fine Science Tools | 11270-20 | |
| ETHILON Nylon Suture | Ethicon | 698H | |
| Fine Scissors - ToughCut | Fine Science Tools | 14058-09 | |
| Hypoallergenic Surgical Tape | 3M Blenderm | 70200419342 | |
| Induction Chamber, 2 Liter | VetEquip | 941444 | |
| Isoflurane | Baxter | 1001936060 | |
| Nair | Church & Dwight Co., Inc | 40002957 | chemical hair removing agent |
| NORADRENALINE RESEARCH ELISA | Labor Diagnostika Nord (Rocky Mountain Diagnostics) | BA E-5200 | |
| NSG Mouse | Jackson Laboratory | JAX:005557 | |
| Povidone-Iodine Swabstick | PDI | S41350 | |
| Webcol Alcohol Preps | Covidien | 5110 |
Access restricted. Please log in or start a trial to view this content.