Rodent thymectomy is a valuable technique in immunological research. Here, a protocol for complete thymectomy in adult rats using a mini-sternotomy along with non-invasive intubation and positive pressure ventilation to minimize perioperative morbidity and mortality is described.
Thymectomy in neonatal rodents is an established and reliable procedure for immunological studies. However, in adult rats, complications of hemorrhage and pneumothorax from pleural disruption can result in a significant mortality rate. This protocol is a simple method of rat thymectomy that utilizes a mini-sternotomy and endotracheal intubation. Intubation is accomplished with a non-invasive and easily reproducible method and allows for positive pressure ventilation to prevent pneumothorax and a controlled airway that allows sufficient time for careful thymus dissection to minimize pleural disruption. A 1.5 cm sternal incision decreases contact with mediastinal vessels and pleura, while still providing full visualization of the thymus. Following exposure of the mediastinum, the thymus is removed by blunt dissection under magnification. The pleural space is then sealed by suture closure of the pre-tracheal muscles followed by the application of surgical glue. The thorax is then closed by suture closure of the sternum, followed by suture closure of the skin. All thymectomies were complete as evidenced by immunohistochemical (IHC) staining of mediastinal tissue, and absence of naïve T-cells by flow cytometry, and the procedure had a 96% survival rate. This method is suitable when complete thymectomy with minimal complications is desired for further immunological studies in athymic adult rats.
Since the early 1960s, the thymus has been recognized for its critical role in the development of central immunological tolerance. Rodent thymectomy has proven to be an essential procedure in defining the role of the thymus in lymphocyte differentiation, self-tolerance, and immunotolerance in the setting of allograft transplantation and tumor metastasis. Removal of the rat thymus allows for studies involving T-cell depletion or the adoptive transfer of defined T cell populations without the re-emergence of native naïve T cells.
Thymectomies in neonatal rodents can be accomplished using a suction technique with reliable outcomes1. In adult rats, this technique is associated with an approximate 20% mortality rate and frequently results in an incomplete thymectomy2. To consistently achieve complete thymectomy in adult rats, open exposure of the mediastinum through a median sternotomy is required. However, this procedure is associated with complications that include tracheal injury, hemorrhage and pneumothorax leading to an overall mortality rate ranging from 1.5 – 6%2-4.
Over the last two decades improvements in thymectomy techniques have decreased perioperative complications and have improved survival rates. Endotracheal intubation allowing for positive pressure ventilation has lessened pneumothorax rates5. Methods of intubation previously described range from open exposure to the trachea to less invasive methods using direct vocal cord visualization. Complications associated with the intubation procedure include tracheal injury, vocal cord rupture, unintended esophageal intubation, and hemorrhage resulting from cardiac puncture or laceration of the superior vena cava. In addition, close proximity of the lower thymic lobes to the pleural lining can result in pneumothorax.
Here we describe a technique of thymectomy through a minimally invasive 2 cm skin incision following a simple method of endotracheal intubation using a blunted-end angiocatheter and transcutaneous tracheal illumination. The thymectomy involves a 1.5 cm sternotomy and a three-layer closure with surgical glue application to seal the mediastinum and minimize the incidence of hemorrhage and respiratory complications. This method reliably results in complete thymectomy as evidenced by the disappearance of CD4+ and CD8+ naïve T cells following thymectomy and the absence of thymic tissue on IHC staining. Operative times and peri-procedural mortality are kept to a minimum.
NOTE: All experimental procedures involving the use of rats were done in accordance with protocols approved by the Animal Care and Use Committee of Duke University.
1. Preparation of the Tracheal Intubation Cannula
2. Pre-Surgical Procedures
3. Intubation
4. Thoracotomy and Thymectomy
This procedure was performed on adult Lewis rats (n = 26). The mean operation time was 15 ± 3 min. There was no intraoperative mortality. The mean intubation time – from placement of rat on the intubation apparatus to establishment of ventilation – was 45 ± 5 sec. 24 rats had a full recovery from the operation with no evidence of respiratory difficulties or hemorrhage through post-operative day (POD) 14. One rat developed respiratory difficulty on POD 4 and underwent re-operation to explore the mediastinum. The rat was found to have a collapsed lung lobe. Following re-expansion of the lung, the mediastinum was re-sealed with surgical glue under positive pressure ventilation and the chest was re-closed. The rat recovered with fully with no further respiratory abnormalities. One rat died on POD 7 of unknown causes.
The post-thymectomy mediastinum was inspected for retained thymus and the removed thymus tissue was visually inspected for missing sections and later examined histologically. At necropsy, thoracic tissue was examined by hematoxylin-eosin (H&E) stain. Immunohistochemistry (IHC) for cytokeratin was then performed to differentiate remnant thymic tissue from thoracic lymph nodes (LN), focusing particularly on sections with higher levels of nuclear staining by H&E as is normal for thymus tissue. Cytokeratin staining was performed using rabbit pan anti-cytokeratin as the primary ab, followed by biotinylated goat anti-rabbit IgG and Vectastain Elite ABC Kit Slides were counter-stained with haematoxylin prior to microscopy evaluation. Thymic tissue can be distinguished from thoracic LNs by denser nuclear staining on H&E (Figure 3A & 3B) and a characteristic lacy pattern of cytokeratin staining, which differs from the absence of cytokeratin staining seen in LNs (Figures 3C & 3D).
Peripheral blood samples obtained from euthanized rats were analyzed for persistent depletion of naïve T cells. Briefly, red blood cells were lysed with ACK lysing buffer and peripheral blood leucocytes (PBLs) were washed twice with PBS 2% FBS prior to stained with antibodies for 30 min at 4 °C. PBLs were then fixed with 4% w/v paraformaldehyde in neutral pH-buffered saline prior to analysis by multi-color flow cytometry. Total T-cells were identified by staining PBMCs (peripheral blood mononuclear cells) with anti-CD45+ and CD3+, and naïve T cells were identified by staining with anti-CD45RC, anti-CD62L and either anti-CD4 or anti-CD8. The percentages of each T cell subpopulation were multiplied by the absolute lymphocyte count (obtained by Duke Vet Clinical Diagnostic Lab) to determine cell counts. Representative Naïve CD4+ and CD8+ T-cell and total T-cell counts are shown in Figure 4. Thymectomized rats maintained overall T-cell counts compared to control rats but demonstrated loss of the naïve T-cell populations.
Figure 1. Design of the intubation cannula. The cannula is formed by blunting the end of the stylet of a 14 G x 2 inch angiocatheter. The distal 3 mm of the stylet is slightly bent to guide the catheter ventrally to facilitate tracheal intubation. (A) Side view of metal stylet. (B) Side view of angiocatheter over stylet. (C) Magnified view of blunted tip of stylet.
Figure 2. A sloped intubation platform is used to position the rat for intubation. The rat is suspended from the metal bar of the intubation platform by its upper incisor teeth. A light source will then be positioned ventral to the rat’s neck to trans-illuminate the pharynx. Forceps are used to hold the tongue and expose the aperture of the larynx. (A) Top view and (B) side view of intubation platform. (C) Diagram of the visualization of the glottis after suspension of the rat and exposure of the larynx. The larynx in the diagram is from a slide purchased from Motifolio.
Figure 3. H&E and cytokeratin staining of mediastinal tissue can distinguish thymus from lymph nodes. Hematoxylin and eosin (H&E) staining of a normal thymus (A) and thoracic LN (B). Cytokeratin staining of thymic tissue (C) and a thoracic LN recovered post-thymectomy (D). Magnification is 200X. Bar is 100 μM. Please click here to view a larger version of this figure.
Figure 4. Attrition of peripheral blood naïve T cells post-thymectomy. Total T cell, naïve CD4+ T cells and naïve CD8+ T cells where quantified from PBLs by flow cytometry in pre-thymectomy (Pre) and rats 4 weeks post-thymectomy (Post). Data are shown for one rat per group and are representative of overall results obtained.
The present protocol for complete thymectomy provides a minimally invasive approach with a three layer incision closure with surgical glue application designed to minimize complications. Complete removal of the thymus was demonstrated by the loss of naïve T cells and by IHC staining of mediastinal lymphoid tissue for cytokeratin.
The procedure of adult rat thymectomy has been complicated by mortality rates ranging from 1.5 – 20% due to peri-operative complications, most of which are the attributable to the intimate association of the lower lobes of the thymus with the pleura, the heart and the major mediastinal vessels2-4. Open tracheal intubation techniques, where the trachea is punctured, have a 6% mortality rate2. The use of non-invasive tracheal intubation has been reported by Na and co-workers; however, survival rates were not reported5. Intubation with the cannula prepared as described here with transcutaneous tracheal illumination permits clear visualization of the vocal cords for consistently successful intubations. No advanced equipment is needed for the presented method, which differs from other reported non-invasive techniques2,5-8. Our method of blunting the end of an angiocatheter needle and creating an upward bend at the end makes it easier to avoid inadvertent esophageal intubation and minimizes tracheal trauma. These are improvements to a previously described method of intubation also using a modified angiocatheter9.
We find that keeping the sternal incision to a minimum decreases contact with major mediastinal vessels and associated risk of hemorrhage while allowing adequate exposure for complete removal of the thymus. Theoretically, the smaller incision should also lessen post-procedural pain and recovery time. The use of fibrin glue was first reported as a modification of an open tracheal intubation procedure to prevent pneumothorax and airway injury2. We have found that the application of a small amount of glue over the sutured pre-tracheal muscles while applying positive pressure adequately seals the pleural cavity and helps to prevent post-operative respiratory complications.
There are a few aspects of the protocol that are important to highlight so the procedure can be performed successfully. It is important to secure the anesthesia tubing with adequate tape because it is possible to disconnect the gas flow during the operation as the surgeon’s hands are positioned near the rat’s head and visualization is focused only on the surgical site under the microscope. The minimum possible lubrication applied to the cannula prior to intubation prevents the cannula from slipping into the esophagus. During the multi-layer closure, it also helps to apply the cyanoacrylate tissue adhesive through a small gauge needle with a syringe, which allows precise application and prevents accidental over-application of glue.
This procedure does not allow re-vascularization of the removed thymus in a recipient rat, which has been described elsewhere10. We also did not attempt this procedure in mice, which are often used for immune studies. The most recent descriptions of the thymectomy procedure in adult mice involve either vacuum aspiration of the thymus after exposure, which has high complication rate in adult rats, or a dissection method that is similar to our procedure11,12. The closure is not performed in layers, and anesthesia is achieved by intraperitoneal injection of pentobarbital, which does not mandate intubation. The main limitations of the thymectomy procedure in any rodent are the requirement for an operating microscope, which can be very expensive, and the technical expertise needed to operate under magnification and perform the procedure quickly.
Complete thymectomy in adult rats facilitates immunological studies involving T-cell development, T cell reactivity and tolerance in transplantation and tumor studies, and studies involving T-cell depletion in athymic rats13-15.
The authors have nothing to disclose.
This work was supported by AI101263 from the National Institutes of Health (T.V.B), and by a grant from The Hartwell Foundation (M.L.M). M.L.M. is a member of the Duke Comprehensive Cancer Center.
Name of Reagent/ Equipment | Company | Catalog Number | Comments/Description |
2" 14-gauge angiocatheter | |||
Operating microscope | Zeiss | ||
Warming pad | |||
Heart rate and blood oxygenation monitor for rodents with foot sensors | Harvard Apparatus | ST1 72-8010, ST1 72-8098 (Rat foot sensor) | |
Intubation apparatus (plastic with metal bar at the top) | See Figure 2 | ||
Small animal anesthesia system with induction box, isoflurane tank and O2 tank | Harvard Apparatus | ST1 72-6420 | |
Small animal ventilator with tubing | CWE | 12-02000 (ventilator)and 12-04000 (external valve assembly for mice/rats) | |
High-intensity Fiber-Optic Illuminator | Dolan Jenner | EEG 2823M | |
Student standard pattern forceps | Fine Science Tools | 91100-16 | |
Fine straight scissors | Fine Science Tools | 14060-09 | |
Blunt-tipped Shea scissors | Fine Science Tools | 14105-12 | |
Small Alm retractor (for sternum) | Fine Science Tools | 17008-07 | |
Blunt Graefe forceps | Fine Science Tools | 11050-10 | |
Fine Dumont forceps | Fine Science Tools | 11254-20 | |
5-0 Maxon sutures | Ethicon | ||
4-0 Silk sutures (with cutting needle) | Ethicon | ||
6-0 Nylon suture | Ethicon | ||
Cyanoacrylate glue (Endermil) | |||
Lubrication gel | Akorn Animal Health | NDC 17478-162-35 |