A Fibrin-Enriched and tPA-Sensitive Photothrombotic Stroke Model

Summary

Traditional photothrombotic stroke (PTS) models mainly induce dense platelet aggregates of a high resistance to tissue plasminogen activator (tPA)-lytic treatment. Here a modified murine PTS model is introduced by co-injecting thrombin and photosensitive dye for photoactivation. The thrombin-enhanced PTS model produces mixed platelet:fibrin clots and is highly sensitive to tPA-thrombolysis.

Abstract

An ideal thromboembolic stroke model requires certain properties, including relatively simple surgical procedures with low mortality, a consistent infarction size and location, precipitation of platelet:fibrin intermixed blood clots similar to those in patients, and an adequate sensitivity to fibrinolytic treatment. The rose bengal (RB) dye-based photothrombotic stroke model meets the first two requirements but is highly refractory to tPA-mediated lytic treatment, presumably due to its platelet-rich, but fibrin-poor clot composition. We reason that combination of RB dye (50 mg/kg) and a sub-thrombotic dose of thrombin (80 U/kg) for photoactivation aimed at the proximal branch of middle cerebral artery (MCA) may produce fibrin-enriched and tPA-sensitive clots. Indeed, the thrombin and RB (T+RB)-combined photothrombosis model triggered mixed platelet:fibrin blood clots, as shown by immunostaining and immunoblots, and maintained consistent infarct sizes and locations plus low mortality. Moreover, intravenous injection of tPA (Alteplase, 10 mg/kg) within 2 h post-photoactivation significantly decreased the infarct size in T+RB photothrombosis. Thus, the thrombin-enhanced photothrombotic stroke model may be a useful experimental model to test novel thrombolytic therapies.

Introduction

Endovascular thrombectomy and tPA-mediated thrombolysis are the only two U.S. Food and Drug Administration (FDA)-approved therapies of acute ischemic stroke, which afflicts ~700,000 patients annually in the United States¹. Because the application of thrombectomy is limited to large vessel occlusion (LVO), while tPA-thrombolysis may alleviate small vessel occlusions, both are valuable therapies of acute ischemic stroke². Moreover, the combination of both therapies (e.g., initiation of tPA-thrombolysis within 4.5 hours of stroke onset, followed by thrombectomy) improves reperfusion and the functional outcomes³. Thus, optimizing thrombolysis remains an important goal for stroke research, even in the era of thrombectomy.

Thromboembolic models are an essential tool for preclinical stroke research aiming to improve thrombolytic therapies. This is because mechanical vascular occlusion models (e.g., intraluminal suture MCA occlusion) do not produce blood clots, and its fast recovery of cerebral blood flow after the removal of mechanical occlusion is overly idealized^4,5. To date, major thromboembolic models include photothrombosis^6,7,8, topical ferric chloride (FeCl₃) application⁹, microinjection of thrombin into the MCA branch^10,11, injection of ex vivo (micro)emboli into the MCA or common carotid artery (CCA)^12,13,14, and transient hypoxia-ischemia (tHI)^15,16,17,18. These stroke models differ in the histological composition of ensuing clots and the sensitivity to tPA-mediated lytic therapies (Table 1). They also vary in the surgical requirement of craniotomy (needed for in situ thrombin injection and topical application of FeCl₃), the consistency of infarct size and location (e.g., CCA-infusion of microemboli yield very variable outcomes), and global effects on the cardiovascular system (e.g., tHI increases the heart rate and cardiac output to compensate for hypoxia-induced peripheral vasodilation).

The RB dye-based photothrombotic stroke (PTS) model has many attractive features, including simple craniotomy-free surgical procedures, low mortality (typically < 5%), and a predictable size and location of infarct (in the MCA-supplying territory), but it has two major limitations.⁸ The first caveat is weak-to-nil response to tPA-mediated thrombolytic treatment, which is also a drawback of the FeCl₃ model^7,19,20. The second caveat of PTS and FeCl₃ stroke models is that the ensuing thrombi consist of densely-packed platelet aggregates with a small amount of fibrin, which not only lead to its resilience to tPA-lytic therapy, but also deviates from the pattern of intermixed platelet:fibrin thrombi in acute ischemic stroke patients^21,22. In contrast, the in situ thrombin-microinjection model mainly comprises polymerized fibrin and a uncertain content of platelets¹⁰.

Given the above reasoning, we hypothesized that admixture of RB and a sub-thrombotic dose of thrombin for MCA-targeted photoactivation through thinned skull may increase the fibrin component in the resultant thrombi and boost the sensitivity to tPA-mediated lytic treatment. We have confirmed this hypothesis,²³ and herein we describe detail procedures of the modified (T+RB) photothrombotic stroke model.

Protocol

This protocol is approved by the Institutional Animal Care and Use Committee (IACUC) at the University of Virginia and follows the National Institutes of Health Guideline for Care and Use of Laboratory Animals. Figure 1A outlines the sequence of surgical procedures of this protocol.

1. Surgery setup

1. Place a warming pad with temperature setting at 37 °C on the small animal adaptor at least 15 minutes before the surgery. Prepare a nose-clip roll for adaptor which allows the animal head rotation. Prepare the anesthetics Ketamine (60 mg/kg)/ Xylazine (10 mg/kg).
2. Sterilize the surgical tools including scissors, forceps, micro-needle holders, hemostats, cotton swabs and sutures with autoclave (121 °C at 15 psi for 60 min). Prepare tissue glue and eye ointment. Prepare the 532 nm laser protection goggle for surgeons.
   NOTE: This protocol describes a major survival surgery procedure and should be conducted using aseptic techniques.
3. Set up the illumination system with a 532 nm laser source. Prepare a dental drill.
4. Prepare the Rose Bengal solution in saline (10 mg/mL). Place an aliquot bovine thrombin (0.1 U/µL) on ice-bucket.
5. Inject Ketoprofen (4.0 mg/kg) subcutaneously to the mouse as analgesia at 30 min before surgery or use the analgesic regimen recommended by the local institutional guidelines.

2. Ligation of the ipsilateral common carotid artery

1. Anesthetize 10-14 week-old male C57BL/6NCrl mice weighing 22 to 30 g by intramuscular injection of Ketamine (60 mg/kg) and Xylazine (10 mg/kg).
   NOTE: The entire surgical procedure, encompassing the ligation of the ipsilateral common carotid artery through the monitoring of cerebral blood flow, is expected to take ~120 min. The anesthetic regimen will be typically effective for this entire duration, but the anesthetic depth should be reassessed at least every 15 min. While learning these procedures, it may be necessary to re-dose the anesthesia.
2. Perform a toe-pinch to ensure the animal is fully anesthetized. Remove the hair on the left neck for CCA ligation and the head for skull thinning with the hair removal cream.
3. Place the mouse on the small animal adaptor in the supine position. Sterilize the surgical area by wiping skin with three alternating swipes of povidone-iodine and 70% ethanol.
4. Secure the mouse head using ear bars. Under a dissecting microscope, make a 0.5 cm left-cervical incision using a pair of micro-scissors and straight forceps at about 0.2 cm lateral to the midline.
5. Use a pair of fine serrated forceps to pull apart the soft tissue and fascia to expose the left common carotid artery (LCCA). Carefully separate the left CCA from the vagal nerve using a pair of fine smooth forceps.
6. Place a permanent double-knot suture around the LCCA using 5-0 silk suture cut into 20 mm segments, and then close the wound using sterile wound clips.

3. Skull thinning above the MCA branch and photoactivation

1. Flip the mouse to prone position on the small animal adaptor. Rotate the nose-clip roll for 15°. Sterilize the surgical area by wiping skin with three alternating swipes of betadine and 70% ethanol.
2. Make a 0.8 cm incision in the scalp using a pair of micro-scissors and straight forceps along the left eye and ear to expose the temporalis muscle, which is located between the eye and the ear (Figure 1B).
3. Under the dissecting microscope, make a 0.5 cm incision along the edge of temporalis muscle on left parietal bone by a pair of fine serrated forceps. Make a second 0.3 cm vertical incision on temporalis muscle by a micro scissors. Retract the temporal muscle to expose the edge of parietal bone and squamosal bone. Make sure to visualize the landmark of coronal suture between the frontal and the parietal bones (Figure 1B,C).
4. Moisture the skull by applying sterile saline to reveal the left MCA. Mark the proximal MCA branch on the squamosal bone with a marker pen. Gently draw a circle for about 1 mm in diameter surrounding the marked area with the pneumatic dental drill (burr speed setting at 50% of speed controller), and then thin the skull about 0.2 mm in depth without touching the underneath dura. Stop the drilling until a very thin layer of bone is left.
5. Mix the thrombin (T, 0.1 U/μL, 80 U/kg) and Rose bengal (RB, 10 mg/mL, 50 mg/kg) solution based on the mouse’s body weight. For example, for a mouse of 25 g body weight, mix 20 μL of thrombin (0.1 U/μL) and 125 μL of RB (10 mg/mL).
6. Slowly inject T+RB solution (145 µL per 25 g body weight) into the retro-orbital sinus with an insulin syringe (#31G needle).
   NOTE: In pilot experiments, the mortality rate of increasing doses of thrombin mixed with the standard dose of RB dye (50 mg/kg) was examined for photoactivation. The mortality was 0% for 80 U/kg thrombin (n=13), 43% for 120 U/kg thrombin (n=7), and 100% for both 160 U/kg (n=5) and 200 U/kg thrombin (n=5). A dose of 80 U/kg thrombin was therefore chosen for this model. Laser speckle contract imaging was also used to exclude the possibility of rampant blood clotting near the orbital cavity after retro-orbital sinus injection of T+RB (Supplementary Figure 1), as well as, widespread fibrin deposition in the contralateral hemisphere that was not subjected to laser illumination (Supplementary Figure 2).
7. Apply eye ointment on both eyes to prevent dryness.
8. Apply the illuminator with a 532 nm laser light (with 0.5 mW energy) on the drilled site with 2-inch distance for 20 min. Visualize the illumination on the proximal branch of MCA through a laser protection goggle (Figure 1C,D).
   NOTE: The MCA with 532 nm illumination shows red fluorescence under the goggle. The distal MCA will disappear after 10 min illumination. Exclude the animal if the distal MCA flow is still present after 20 min illumination.
9. Stop the laser illumination after 20 min. Close the wound with sterile wound clips.

4. Intravital imaging (optional)

NOTE: To characterize the thrombus formation in-vivo, use intraviral imaging by a spin-disk confocal with photoactivation system²³.

1. Make a cranial window ~3 mm in diameter on the parietal bone of skull.
2. Place a coverglass on the cranial window and locate the distal MCA (~50 μm in diameter) under a 20x water-immersion objective.
3. Label the circulating platelet by tail vein injection of DyLight488-conjugated anti-GPIbβ antibody (0.1 mg/kg) at 5 min before imaging.
4. Inject the mixture solution of thrombin (80 U/kg) and Rose bengal (50 mg/kg) by retro-orbital at 5 min before imaging.
5. Photoactivate the MCA using a 561 nm laser system with laser beam 10 μm in diameter and record the image until the thrombus formation.

5. tPA administration

1. Place the anesthetized animal on a 37 °C warm pad. At the selected post-photoactivation time-point, wet a gauze with ~45 °C warm water and wrap it on the tail for 1 min.
2. Inject recombinant human tPA (10 mg/kg) through the tail vein with a 50% bolus and 50% over 30 min by infusion pump.
   NOTE: Although the clinical dose of recombinant human tPA for acute ischemic stroke treatment is 0.9 mg/kg, a higher dose (10 mg/kg) is commonly used in rodents to compensate for reduced cross-species tPA reactivity. We also followed the standard protocol of tPA-administration in preclinical stroke models, using 50% as a bolus and 50% infused through the tail vein over 30 min.²⁴

6. Monitor of cerebral blood flow (CBF)

NOTE: To confirm CBF recovery after tPA treatment, use a two-dimensional laser speckle contrast imaging system¹⁵ and record immediately after photothrombosis (step 3.9) or at 24 h after tPA treatment.

1. Place anesthetized animal in the prone position and make a midline incision on the scalp with the skull exposed.
2. Moisturize the skull with sterile saline and gently apply the ultrasound gel on the skull. Avoid any hair and bubble in the gel, which will interfere the CBF signal.
3. Monitor CBF in both cerebral hemispheres under laser speckle contrast imager for 10 min.
4. After recording the CBF image, close the scalp with tissue glue and return the animal to the cage.
5. Analyze CBF in the selected regions and calculate the CBF recovery percentage compared to contralateral region.
6. Then, place the animal back to a warm cage for recovery. Monitor the mice for 5-10 min until they recover from anesthesia. Place wetted food in the cage and return it to the animal care facility.
   NOTE: Provide post-op analgesia as recommended by the local institutional guidelines.

7. Infarct volume measurement by triphenyl tetrazolium chloride (TTC) staining

1. Twenty-four hours after photothrombosis, deeply anesthetize the animal per the local institutional guidelines for nonsurvival surgery.
   NOTE: We administer tribromoethanol (avertin) 250 mg/kg via intraperitoneal (IP) injection.
2. Perform transcardial perfusion with PBS, collect fresh brain and embed in 3% agar gel.
3. Section the brain slice with 1 mm thickness by vibratome and incubate in 2% TTC solution for 10 min.
4. Quantify the total infarct volume from 6 brain slices as the absolute volume by ImageJ software.
   NOTE: Brain edema was not used as an outcome measurement for two reasons. First, the TTC stain measures tissue viability (via the mitochondrial reduction activity) which is a more severe consequence than edema. Second, as infarction proceeds, both vasogenic and cytotoxic edema occur and cannot be easily distinguished by the standard brain edema measurement methods. However, we have used anti-immunoglobin (IgG) labeling to assess the integrity of blood-brain-barrier (BBB), and found comparable IgG-extravasation at 6 h after photoactivation in both RB and T+RB stroke models (Supplementary Figure 3).

8. Thrombus formation measurement

NOTE: To measure the thrombus formation, collect the brain at 1 h and 2 h after photothrombosis for thrombus measurement in MCA by immunochemistry (IHC) and for fibrin measurement in brain hemisphere by immunoblot, respectively.

1. Perform the IHC for the characterization of clot composition. Fix the brain with 4% paraformaldehyde overnight and then dehydrate the brain with 30% sucrose for the OCT embedding.
2. Section the brain with sagittal orientation in 20 μm thickness, and perform the IHC with specific antibodies against fibrinogen, platelet (glycoprotein IIb), red blood cell (TER119) and blood vessel (isolectin GS-IB4).
3. Perform the measurement of fibrin in brain hemisphere by immunoblot with an antibody against fibrinogen.

Results

First, we compared the fibrin content in RB versus T+RB photothrombosis-induced blood clots. Mice were sacrificed by transcardial perfusion of fixatives at 2 h after photoactivation, and brains were removed for immunofluorescence staining of the MCA branch in longitudinal and transverse planes. In RB photothrombosis, the MCA branch was densely packed with CD41⁺ platelets and little fibrin (Figure 2A,C). In contrast, the MCA branch in T+RB photothrombosis was occlu...

Discussion

The traditional RB photothrombotic stroke, introduced in 1985, is an attractive model of focal cerebral ischemia for simple surgical procedures, low mortality, and high reproducibility of brain infarction.⁵ In this model, the photodynamic dye RB rapidly activates platelets upon light excitation, leading to dense aggregates that occlude the blood vessel^5,8,23. However, the small amount of fibrin in RB-indu...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
2,3,5-triphenyltetrazolium chloride (TTC)	Sigma	T8877	infarct
4-0 Nylon monofilament suture	LOOK	766B	surgical supplies
5-0 silk suture	Harvard Apparatus	624143	surgical supplies
543nm laser beam	Melles Griot	25-LGP-193-249	photothrombosis
adult male mice	Charles River	C57BL/6	10~14 weeks old (22~30 g)
Anesthesia bar for mouse adaptor	machine shop, UVA		surgical setup
Avertin (2, 2, 2-Tribromoethanol)	Sigma	T48402	euthanasia
Dental drill	Dentamerica	Rotex 782	surgical setup
Digital microscope	Dino-Lite	AM2111	brain imaging
Dissecting microscope	Olympus	SZ40	surgical setup
Fine curved forceps (serrated)	FST	11370-31	surgical instrument
Fine curved forceps (smooth)	FST	11373-12	surgical instrument
goat anti-rabbit Alexa Fluro 488	Invitrogen	A11008	Immunohistochemistry
Halsted-Mosquito hemostats	FST	13008-12	surgical instrument
Heat pump with warming pad	Gaymar	TP700	surgical setup
infusion pump	KD Scientific	200	thrombolytic treatment
Insulin syringe with 31G needle	BD	328291	photothrombosis
Ketamine	CCM, UVA		anesthesia
Laser protective google 532nm	Thorlabs	LG3	photothrombosis
Ketoprofen	CCM, UVA		NSAID analgesia
micro needle holders	FST	12060-01	surgical instrument
micro scissors	FST	15000-03	surgical instrument
MoorFLPI-2 blood flow imager	Moor	780-nm laser source	Laser Speckle Contrast Imaging
Mouse adaptor	RWD	68014	surgical setup
Puralube Vet ointment	Fisher	NC0138063	eye dryness prevention
Retractor tips	Kent Scientific	Surgi-5014-2	surgical setup
Rose Bengal	Sigma	198250	photothrombosis
Thrombin	Sigma	T7513	photothrombosis
Tissue glue	Abbott Laboratories	NC9855218	surgical supplies
tPA	Genetech	Cathflo activase 2mg	thrombolytic treatment
Vibratome	Stoelting	51425	TTC infacrt
Xylazine	CCM, UVA		anesthesia