Assessment of Blood-brain Barrier Permeability by Intravenous Infusion of FITC-labeled Albumin in a Mouse Model of Neurodegenerative Disease

Summary

In this study, we present an easy and efficient procedure for evaluating the disruption of the blood-brain barrier under neurodegenerative conditions. To achieve our objective, we infused high molecular weight fluorescein isothiocyanate labelled (FITC)-albumin into mouse jugular vein and evaluated its leakage into the brain parenchyma by fluorescence microscopy.

Abstract

Disruption of blood-brain barrier (BBB) integrity is a common feature for different neurological and neurodegenerative diseases. Although the interplay between perturbed BBB homeostasis and the pathogenesis of brain disorders needs further investigation, the development and validation of a reliable procedure to accurately detect BBB alterations may be crucial and represent a useful tool for potentially predicting disease progression and developing targeted therapeutic strategies.

Here, we present an easy and efficient procedure for evaluating BBB leakage in a neurodegenerative condition like that occurring in a preclinical mouse model of Huntington disease, in which defects in the permeability of BBB are clearly detectable precociously in the disease. Specifically, the high molecular weight fluorescein isothiocyanate labelled (FITC)-albumin, which is able to cross the BBB only when the latter is impaired, is acutely infused into a mouse jugular vein and its distribution in the vascular or parenchymal districts is then determined by fluorescence microscopy.

Accumulation of green fluorescent-albumin in the brain parenchyma functions as an index of aberrant BBB permeability and, when quantitated by using Image J processing software, is reported as Green Fluorescence Intensity.

Introduction

Homeostasis within the central nervous system (CNS) is a prerequisite for the proper communication and function of the neuronal cells. The CNS parenchyma is tightly sealed off from the periphery by the endothelial blood-brain barrier (BBB), which represents the interface between the peripheral bloodstream and the brain and plays a pivotal role in the cross-talk between these two districts^1,2. The BBB is a complex and dynamic three-dimensional structure mainly composed of specialized micro-vessel endothelial cells (ECs) linked to each other through intercellular junctional complexes - tight junctions (TJs)- and surrounded by pericytes, neuron endings and astrocyte foot processes^1,2.

Under physiological conditions, the extremely low permeability of the intact BBB ensures the strict regulation of the transport of nutrients and other molecules into and out of the brain, and provides the CNS with a unique protection from changes occurring in the composition of the blood that might influence neural activity and against potential peripheral insults^1,2,3.

Disruption of BBB integrity and its enhanced permeability has long been known to constitute a key feature for many neurological and neurodegenerative disorders⁴ including Huntington's Disease (HD)^5,6, however, whether such a dysfunction is a causative phenomenon or a propagative event in the course of the disease is still unclear. The timing of BBB breakdown also remains elusive, however, emerging evidence by our group and others indicates that disrupted BBB integrity does not represent a late event in the disease progression, but rather an early step^6,7,8, which may have long-term consequences.

With this in mind, it is important to precociously reveal BBB breakdown in neurodegeneration in order to develop strategies useful to predict disease progression and brain damage and to develop alternative and more targeted interventions capable of successfully mitigating the clinical consequences of such a disruption. Reliable imaging of BBB impairment is, therefore, of major importance in both experimental research and clinical management of brain diseases.

In this paper, we describe a successful and simple procedure for the evaluation of BBB permeability in a HD mouse model by using the high molecular weight fluorescein isothiocyanate labelled-albumin (FITC-albumin). Extravasation of FITC-albumin, which normally cannot cross the barrier, into the brain parenchyma was measured as an index of BBB leakage. This technique is readily adaptable to rats and to other pathological conditions characterized by cerebrovasculature impairment^9,10.

Protocol

All procedures on animals were approved by the IRCCS Neuromed Animal Care Review Board and by "Istituto Superiore di Sanità" (permit number: 1163/2015- PR) and were in accordance with the guidelines of the EU Directive 2010/63/EU for animal experiments.

1. Preparation of FITC-albumin Solution to be Injected into Jugular Vein

NOTE: All experiments were carried out in manifest (11-week old) HD R6/2 mice and in age and gender-matched wild-type (WT) control littermates.

1. Dissolve FITC-albumin powder (see Table of Materials) in phosphate buffered saline (PBS) at 10 mg/ml.
   NOTE: For optimal results, this should be prepared fresh for each labelling reaction.

2. Preparation of Equipment to Be Used During Surgery

1. Lay out the previously autoclaved surgical instruments (see Table of Materials).
2. Clean the surgical bench with alcohol (70% ethanol solution). Prepare the surgical area (45 cm x 45 cm) with a surgical sterile disposable towel drape and set up the operating stereomicroscope.

3. Surgical Procedure for FITC-albumin Infusion into the Jugular Vein

1. Record mouse body weight for anesthesia.
2. Anesthetize mouse with an intraperitoneal injection (i.p) of an appropriate dose of Ketamine (100 mg/kg) - xylazine (10 mg/kg) solution.
3. Monitor animal sedation by gentle toe pinch withdraw reflex as demonstrated in Walantus et al.^11,12.
4. Place the anesthetized mouse in a face-up supine position and fix the four legs and the tail on the surgical workbench with adhesive tape.
5. After the mouse is secured, carefully shave the appropriate surgical margin on the neck with an electric razor (see Table of Materials) and disinfect it with povidone-iodine solution and 70% ethanol.
6. Dry the exposed shaved surface with cotton swabs.
7. Gently pull up the shaved skin and make a 1.5 cm long longitudinal incision, by scalpel, in the midclavicular line starting midway on the thorax and extending to just below the neck.
8. Carefully stretch apart connective tissue with forceps under microscopic observation (5X magnification) to expose the external jugular vein.
9. Ensure a sufficient space on the right and on the left of the jugular vein to facilitate the insertion of the 30½ G needle for the infusion of the FITC-albumin solution.
10. Inject the animal intravenously (right jugular vein) slowly (over 3 min) with 100 µL of 10 mL/kg FITC-albumin by using the 30½ G needle.
11. After 15 minutes, euthanize the mouse by decapitation, rapidly remove the brain from the skull as previously described¹³, and immerse it for 15 min in at least 10x the volume of the brain itself of pre-chilled isopentane.
12. Move the isopentane frozen brain into a pre-chilled tube and store it into a -80 °C freezer until histological sectioning.

4. Histological Sectioning of Brain Infused with FITC-albumin

1. Embed frozen brain in optimal cutting temperature (OCT) compound (see Table of Materials) prior to cryostat sectioning.
2. Serially cut the brain into 20 µm thick sections, with a cryostat (see Table of Materials), and mount them onto microscope glass slides.
3. Perform the FITC-Albumin/laminin co-staining by using a specific anti-laminin antibody (see Table of Materials) as previously described⁶.
   1. Briefly, incubate sections with the primary antibody anti-laminin (pAb 1:1000) over night and proceed with appropriate secondary antibody conjugated to Cy3.
   2. Coverslip slides with mounting medium containing 4',6-diamidino-2-phenylindole (DAPI) (absorption peak = 360 nm; emission peak = 460 nm (see Table of Materials).
   3. Leave the slide to dry overnight at 4 °C in the dark.
   4. Observe the fluorescence staining under a fluorescence microscope (see Table of Materials) at 20X magnification equipped with both FITC (absorption peak = 495 nm; emission peak = 525 nm) and Cy3 filters (absorption peak = 550 nm; emission peak = 570 nm).
      1. To view the samples immediately after the staining, secure the coverslip at the corners using nail polish and examine them under the microscope as above (4.3.3).

5. Setting Up the Fluorescence Microscope and Acquisition of Colour Images

1. Set up the fluorescence microscope as follows.
   1. Turn on the fluorescence lamp about 10 minutes before use. Turn on the microscope, the connected computer, and the digital camera. Run the image analysis software (see Table of Materials).
   2. Use the appropriate objective for optimal signal collection and spatial resolution, and select appropriate filters.
2. Acquisition of Colour Images
   1. Select the [live] command on the image analysis software (see Table of Materials) and set up the optimal illumination parameters for each filter.
   2. Select the [freeze] command to take the single channel colour image and add the scale bar ('Edit>Burn Scale')
   3. Save each image in the '.tiff' format.
   4. Merge channels into a single image by selecting 'File>Merge channel' and save it in the
   5. tiff' format.
   6. Acquire a minimum of four twenty-four bit color pictures (2200 µm x 3400 µm) per brain slice (6 sections per slide).

6. Assessment of FITC-albumin Extravasation

1. Analyze the fluorescence intensity for each single channel by using the freely available ImageJ^14,15.
2. Normalize the total fluorescent signal intensity of the FITC-albumin by the total CY3-Laminin fluorescent intensity per each image and report the extravasated albumin outside the vessels as Green Fluorescence Intensity.

Results

Proper infusion of FITC-albumin into the jugular vein results in the extravasation of the green fluorescence tracer from the bloodstream into the brain parenchymawhen the BBB is compromised⁶. Under physiological conditions, distribution of infused fluorescent albumin is restricted to the inside of the brain blood vessels and no signal in the surrounding perivascular area and/or brain parenchyma is detectable (Figure 1A, micrographs on ...

Discussion

The technique we describe here is primarily useful for detecting BBB leakage under brain disease conditions. BBB dysfunction is gaining attention as a common feature of diverse neurologic disorders⁴. We previously used this approach to describe the early derangement of BBB integrity in a mouse model of a rare neurodegenerative disease like HD⁶.

This method takes advantage of the relative simplicity and effectiveness of the procedure, which provid...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
Albumin-fluorescin isothiocyanate conjiugate	SIGMA	A9771-100MG
pAb anti-Laminin	Novus Biologicals	NB300-144
CY3 anti-rabbit made in goat	MILLIPORE	AP132
SUPERFROST PLUS	Thermo Scientific	J1800AMNZ
Cover Slips 24 X 50 mm	Thermo Scientific (DIAPATH)	61050
Kilik Optimal Cutting Temperature (OCT) compound	Bio Optica	05-9801
VECTASHIELD Mounting Media	VECTOR	H-1500	Mounting media with DAPI
iNSu/Light Insulin Disposible Syringe	RAYS Health & Safety	INS1ML26G13
30G 1/2"	BD Microlance	304000	Needle for Insulin disposible Syringe
Scalpel Handle	F.S.T.	91003-12
#22 Disposable Scalpel blads	F.S.T.	10022-00
Fine Iris scissors 10.5 cm	F.S.T.	14094-11
Dumont Forceps #5745 45° 0.10 x 0.06 mm	F.S.T.	11251-35
Graefe Forceps 10 cm	F.S.T.	11051-10
Dumont Forceps #5 0.1 X 0.06 mm	F.S.T.	11251-20
Medical patch	Medicalis	34788
Sterile disposable towel drape	Dispotech	TVO50VE
Stereoscopic Microscope	NIKON	SMZ 745 T
Optic Illuminator LED light (C-FLED2)	NIKON	1003167	Optic Illuminator for Stereoscopic Micrscope
Eclipse Ni-U Microscope	Nikon	932162	Epifluorescence Microscope
Microscope digital Camera	Nikon	DS-Ri2	Microscope camera
Intenslight	Nikon	C-HGFI	Microscope lamp
NIS-Elements 64 bit	Nikon	AR 4.40.00	Analysis Software
Electric Razor	Gemei	GM-3007