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Microglia are regarded as some of the most versatile cells in the body, capable of morphological and functional adaptation. Their heterogeneity and multifunctionality enable the maintenance of brain homeostasis, while also being linked to various neurological pathologies. Here, a technique for purifying spinal cord microglia is described.
The vertebral column defines a vertebrate and shapes the spinal canal, a cavity that encloses and safeguards the spinal cord. Proper development and function of the mammalian central nervous system rely significantly on the activity of resident macrophages known as microglia. Microglia display heterogeneity and multifunctionality, enabling distinct gene expression and behavior within the spinal cord and brain. Numerous studies have explored cerebral microglia function, detailing purification methods extensively. However, the purification of microglia from the spinal cord in mice lacks a comprehensive description. In contrast, the utilization of a highly purified collagenase, as opposed to an unrefined extract, lacks reporting within central nervous system tissues. In this study, the vertebral column and spinal cord were excised from 8-10 week-old C57BL/6 mice. Subsequent digestion employed a highly purified collagenase, and microglia purification utilized a density gradient. Cells underwent staining for flow cytometry, assessing viability and purity through CD11b and CD45 staining. Results yielded an average viability of 80% and a mean purity of 95%. In conclusion, manipulation of mouse microglia involved digestion with a highly purified collagenase, followed by a density gradient. This approach effectively produced substantial spinal cord microglia populations.
The defining characteristic of vertebrates is the vertebral column or spine, in which the notochord has been replaced by a sequence of segmented bones called vertebrae, divided by intervertebral discs. This succession of osseous material shapes the spinal canal, a cavity that encloses and protects the spinal cord1. In the genus Rodentia, the spine is usually formed by seven cervical vertebrae, thirteen thoracic vertebrae, six lumbar vertebrae, and a variable number of caudal vertebrae2,3. The length of the spinal cord is similar to that of the spine, and the terminal filum is a....
The study was conducted in accordance with the official Mexican standard NOM-062-ZOO-1999 and the guide for the care and use of laboratory animals. Approval for the study was obtained from the Research, Ethics, and Biosafety Committees of the Mexico Children's Hospital (HIM/2023/006) and the Research and Bioethics Committee of the General Hospital of Mexico Eduardo Liceaga (DI/21/501/04/62). Three C57BL/6 mice aged 6 to 8 weeks were obtained from the Mexico Children's Hospital, where they were raised under isolat.......
Utilizing mouse spinal cord tissue, enzymatic digestion was performed using a mixture highly enriched with collagenase and thermolysin. The resulting digested tissue underwent passage through a 40 µm filter to eliminate undigested material. The collected cells were enriched through a Percoll density gradient, with 90% in the lower portion and 45% in the upper portion. The microglia-enriched cells within the interface were then stained with CD45 and CD11b antibodies and subjected to flow cytometric analysis (
Numerous protocols have been developed for the study of microglia due to their significance in brain homeostasis. In these methods, microglia are typically sourced from the cerebral hemispheres of embryonic or neonatal rats and mice17. A limited number of studies have addressed the purification of microglia from the spinal cords of adult mice13,14. These techniques involve enzymatic digestion using collagenase and/or papain along with DNAs.......
This work was supported by grants from the scholarship granted by the National Council of Science and Technology (CONACYT) (702361). The authors acknowledge the Ph.D. program in Biological Chemical Sciences of the National School of Biological Sciences of the National Polytechnic Institute.
....Name | Company | Catalog Number | Comments |
15 mL collection tubes | Corning, USA | 430790 | |
2 mL microtubes | Axygen, USA | MCT-200-G | |
2.4G2 anti-FcR | BioLegend, USA | 101302 | |
50 mL collection tubes | Corning, USA | 430829 | |
70% ethanol | |||
Antibiotic-Antimycotic (penicillin, streptomycin, amphotericin b) | Gibco, USA | 15240062 | |
Antibody CD11b eFluor 450 anti-mouse | eBioscience, USA | 48-0112 | |
Antibody CD45 PerCP anti-mouse | BioLegend, USA | 103130 | |
Balanced salt solution (PBS) calcium- magnesium-free | Corning, USA | 46-013-CM | |
Blue Cell Strainer 40 μm | Corning, USA | 352340 | |
Costar 6-well Clear Not Treated | Corning, USA | CLS3736 | |
Coverslips | |||
Digital Heating Shaking Drybath | Thermo Scientific Digital HS Drybath, USA | 88870001 | |
Dissecting forceps for microsurgery | FT by DUMONT | ||
DNase | Roche, USA | 4536282001 | |
Dulbecco´s Modified Eagle´s Medium-high glucose (DMEM) | Merck, USA | D6429 | |
Electric shaver | |||
FACS tube | Thermo, USA | 352058 | |
Fetal bovine serum (FBS) | PAN Biotech, Alemania | P30-3306 | |
Flow cytometer Cytoflex | Beckman Coulter | ||
Hank’s balanced salt solution | Merck, USA | H2387 | |
L-glutamine | Corning, USA | 15393631 | |
Liberase TM | Roche, USA | 5401119001 | |
Neubauer chamber Counting Chambers | China | 1103 | |
Pentobarbital | |||
Percoll | Merck, USA | 17089101 | density gradient centrifugation |
Poly-L-lysine solution | Merck, USA | P8920 | |
Scalpel No. 25 | HERGOM, Mexico | H23 | |
Snaplock Microcentrifuge Tubes 2 mL | Axygen, USA | 10011-680 | |
Stereoscopic microscope | Velab, Mexico | HG927831 | |
Straight surgical scissors (10 cm) | HERGOM, Mexico | ||
Straight Vannas scissors | HERGOM, Mexico | ||
Triton X100 | Merck, USA | X100 | |
Trypan blue Stain 0.4% | Merck, USA | 15250-061 | |
Vortex mixer | DLAB, China | 8031102000 | |
Zombie Aqua Fixable Viability Kit | BioLegend, USA | 423102 | amine-reactive fluorescent dye staining |
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