Transplantation into the Anterior Chamber of the Eye for Longitudinal, Non-invasive In vivo Imaging with Single-cell Resolution in Real-time

Podsumowanie

A new approach combining intraocular transplantation and confocal microscopy enables longitudinal, non-invasive real-time imaging with single-cell resolution within grafted tissues in vivo. We demonstrate how to transplant pancreatic islets into the anterior chamber of the mouse eye.

Streszczenie

Intravital imaging has emerged as an indispensable tool in biological research. In the process, many imaging techniques have been developed to study different biological processes in animals non-invasively. However, a major technical limitation in existing intravital imaging modalities is the inability to combine non-invasive, longitudinal imaging with single-cell resolution capabilities. We show here how transplantation into the anterior chamber of the eye circumvents such significant limitation offering a versatile experimental platform that enables non-invasive, longitudinal imaging with cellular resolution in vivo. We demonstrate the transplantation procedure in the mouse and provide representative results using a model with clinical relevance, namely pancreatic islet transplantation. In addition to enabling direct visualization in a variety of tissues transplanted into the anterior chamber of the eye, this approach provides a platform to screen drugs by performing long-term follow up and monitoring in target tissues. Because of its versatility, tissue/cell transplantation into the anterior chamber of the eye not only benefits transplantation therapies, it extends to other in vivo applications to study physiological and pathophysiological processes such as signal transduction and cancer or autoimmune disease development.

Wprowadzenie

Advances in intravital microscopy have revealed physiological phenomena not predicted by in vitro studies¹. This highlights the challenge in translating findings obtained by conventional in vitro methods into the living animal. In the last decade, visualization of tissues in living animals was considerably improved by technological advances in imaging modalities^{2, 3, 4, 5, 6}. This has spurred a need for in vivo imaging approaches with feasible application in experimental animal models to enable longitudinal visualization of target tissues non-invasively.

Imaging techniques such as magnetic resonance imaging and positron emission tomography or bioluminescence have enabled non-invasive imaging of organs/tissues deep within the body^{7-8, 9}. But these techniques cannot achieve single cell-resolution due to high background signals and low spatial resolution, despite the use of high contrast materials or tissue-specific luminescence⁴. This was addressed with the advent of two-photon fluorescence confocal microscopy¹⁰. Two-photon microscopy enabled intravital imaging studies to visualize and quantify cellular events with unprecedented details^{11, 12}. This has led to the characterization of key biological processes in health and disease^{13, 14, 15, 16}. While pioneering intravital imaging studies have primarily "mimicked" in vivo conditions in excised tissue (e.g. lymph nodes), other studies have used invasive approaches to image exposed target tissues in situ^{17, 18, 19, 20, 21}. Other studies have also used "window chamber models" to circumvent limitations associated with invasive approaches and limited imaging resolution in vivo^{22, 23, 24, 25}. In the window chamber model, a chamber with a transparent window is surgically implanted into the skin at different locations (dorsal or ear skin, mammary fat pad, liver, etc) on the animal (e.g. mouse, rat, rabbit). While this approach clearly enables high-resolution in vivo imaging, it requires an invasive surgery to implant the chamber and may not be able to accommodate longitudinal imaging studies over several weeks or months²².

It was recently demonstrated that combining high-resolution confocal microscopy with a minimally invasive procedure, namely transplantation into the anterior chamber of the eye (ACE) provides a "natural body window" as a powerful and versatile in vivo imaging platform^{26, 27}. Transplantation into the ACE has been used in the last several decades to study biological aspects of a variety of tissues ^{28, 29, 30}; and its recent combination with high-resolution imaging enabled studying the physiology of pancreatic islets with single cell-resolution non-invasively and longitudinally^{26, 27}. This approach was used to study autoimmune responses during development of type 1 diabetes in animal models (unpublished data). It was also used to study pancreatic development, as well as, in studies of kidney function by transplanting into the ACE pancreatic buds or individual renal glomeruli, respectively (unpublished data). A recent report using this approach further demonstrated its application to study immune responses after pancreatic islet transplantation³¹. Importantly, this study showed that transplantation into the anterior chamber of the eye provides a natural body window to perform: (1) longitudinal, non-invasive imaging of transplanted tissues in vivo; (2) in vivo cytolabeling to assess cellular phenotype and viability in situ; (3) real-time tracking of infiltrating immune cells in the target tissue; and (4) local intervention by topical application or intraocular injection.

Here, we demonstrate how to perform transplantation into the anterior chamber of the eye using pancreatic islets.

Protokół

The following procedure is performed under the stereoscope in 2 steps, the first step involves loading the islets into the cannula and the second step is the actual transplantation into the ACE. All procedures performed on animals were approved by the institutional animal care and use committee (IACUC) of the University of Miami.

1. Loading Islets in Cannula for Transplantation

1. Center the islets in culture dish by spinning the dish in narrowing circles.
2. Disconnect the cannula from the "reservoir" and place the cannula and connecting tubing on a clean surface. The reservoir can be made out of a 300 μl disposable plastic pipette tip without filter (Figure 1a).
3. Flush air bubbles out of the reservoir to ensure continuous stream of islets when aspirating into reservoir. Flushing the reservoir is done by driving forward the hands-free motorized syringe-driver using the foot pedal (Figure 1b, c). This will also make space in the syringe to allow aspiration of the islets into the reservoir (pre-loaded with sterile solution such as saline, PBS or culture media).
4. Gently aspirate desired amount of islets into the reservoir. Islets will tend to swirl as they enter the reservoir and will remain together towards the bottom. Aspiration is done by driving backward the motorized syringe-driver using the foot pedal.
5. Reconnect the cannula to the reservoir via the connecting tubing.
6. Place the cannula tip back in the culture dish and flush the islets out of the reservoir into the tubing then into the cannula. Ensure that islets remain together as you back-fill the tubing/cannula by gently "flicking" (tapping) the tubing (Figure 1d). Stop either before or after all air bubbles ahead of the islets are flushed out the cannula. If not sure, stop as islets enter the back of the cannula as remaining air bubbles ahead of islets can help prevent reflux (backflow) of islets out of the ACE. Will dissipate overnight.
7. At this stage, you are ready to inject the islets into the ACE (please see next steps).

2. Islet Transplantation into the Anterior Chamber of the Eye

1. Position the anesthetized mouse on a warm pad under stereoscope.
2. Place the snout of the mouse into anesthesia "mask" connected to oxygen/isoflurane anesthesia machine. The mask is made out of a 1 ml disposable plastic pipette tip (without filter) and connected to anesthesia tubing through the narrow end (Figure 2a,b).
3. Gently retract the eye lids of the eye to be transplanted using the index finger and thumb of your free hand and "pop" the eye out for better exposure and easy access (Figure 2c). This will require some practice to perfect without impeding breathing of the mouse by excessive pressure on the neck or blocking blood flow to the head.
4. Using a disposable insulin syringe (29 - 31G) as scalpel, carefully penetrate only the tip in the cornea and make a single lateral incision. Make the incision at midpoint between the apex of the cornea and limbus to minimize reflux of the islets during injection out of the ACE (Figure 2d).
5. Carefully insert the cannula (preloaded with islets) through the incision.
6. Slowly eject islets out of the cannula and deposit them on top of the iris. To avoid islet reflux due to excessive pressure buildup in the ACE, eject the islets in brief thrusts in as little volume(s) as possible in the quadrant opposite to the incision. This can be further ensured by compacting islets in the tubing while loading the cannula (please see step 1.6).
7. Slowly retract the cannula out of the ACE. This is a critical step, especially, if a large volume of islets was injected as islet reflux due to pressure build up inside the ACE may be inevitable. To eliminate/minimize islet reflux, gently rotate the cannula while inside the ACE to release excess pressure through the incision around the cannula. Check for signs of reflux as you attempt to retract the cannula and, if needed, wait until pressure subsides before completely retracting the cannula out of the ACE.
8. Rinse the transplanted eye with sterile PBS or saline.
9. Inject buprenorphine for post-operative analgesia (0.05-0.1 mg/kg, subcutaneously) for the first 48 hr.
10. Apply erythromycin ophthalmic antibiotic ointment to the transplanted eye immediately after transplantation.
11. Place the animal back in a warmed cage to allow recovery from anesthesia.

Wyniki

There are a few parameters that define a "good" transplantation. A good transplantation is one that proceeds without bleeding when making the incision as can be seen in the video. Bleeding is prevented/minimized by penetrating only the tip of the scalpel (needle) into the ACE (Figure 3a). This will also help prevent contact and puncture of the iris. It will also ensure a small incision which will heal very well without causing cloudiness of the cornea over time (Figure 3c, d). Anoth...

Dyskusje

Murine pancreatic islets were isolated using collagenase digestion followed by purification on density gradients, as described previously ³³. Isolated islets were cultured overnight before transplantation. While this may not be required, it is recommended to allow the islets to recover from the isolation procedure. This is critical when transplantation is performed in diabetic recipients as it will ensure transplantation of surviving/robust islets.

Transplantation is performed ...

Materiały

Name	Company	Catalog Number	Comments
IsoTHESIA (Isoflurane)	Buttler Animal Health Supply	11695-6775-2	99.9% Isoflurane/ml
Ketaset (Ketamine HCL)	Fort dodge Animal Health	0856-2013-01	Alternative injectable anesthesia
Beprenex (Buprenorphine HCL)	Reckitt Benckiser Health Care (UK) Ltd.	12496-075-7-1	0.3 mg/ml
Erythromycin Ophthalmic Ointment USP, 0.5%	Akron	17478-070-35	Applied prophylactically to transplanted eye
0.9% Sodium Chloride (Saline)	Hospira Inc.	0409-7983-03	For iv injection. Sterile
PBS	Gibco	10010-023	1X. Sterile
CMRL medium 1066	Cellgro	98-304-CV	Supplemented, CIT modification. Preferred media for islets