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2 protocols using rm5201

1

Isolation and Identification of Muscle Cell Populations

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For isolation of cell populations, tibialis anterior, quadriceps and gastrocnemius muscles were collected uninjured or 3 days after glycerol injection and digested with Dispase II (2.5 U/ml) (Roche), Collagenase B (0.2%) (Roche) and MgCl2 (5 mM) at 37 °C. Cells were then incubated at 4 °C for 30 min with antibodies against CD45 (Invitrogen, MCD4501 or MCD4528; dilution for both 1/25), CD31 (Invitrogen, RM5201 or RM5228; dilution for both 1/25), CD11b (Invitrogen, RM2801 or RM2828; dilution for both 1/25), CD34 (BD Biosciences, 560230 or 560238; dilution for both 1/60), Ly-6A–Ly-6E (Sca1) (BD Biosciences, 561021; dilution 1/150), α7-integrin (R&D, FAB3518N; dilution 1/30) and CD140a (eBioscience, 12–1401–81 or 17–1401–81; dilution for both 1/30). Antibody validation is provided on the manufacturer’s website. Specific cell subsets were isolated with a Beckman Coulter Astrios Cell sorter as described below and represented in supplementary figures S1 and S3A. MuSCs were identified as CD31/CD11b/CD45/Sca1/CD34+/Integrin α7+ and Fibro/Adipogenic progenitors (FAPs) were identified as CD31/CD11b/CD45/Sca1+/CD34+/PDGFRα+. Lineage positive cells (Lin+) were identified as: CD31+/CD11b+/CD45+. CD31/CD11b/CD45/Sca1+/CD34+/PDGFRα cells were also collected and named PDGFRα cells.
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2

Immunophenotyping of Brain Vascular Cells

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Extracellular and intracellular stainings was performed by the method of (Larochelle, C. et al., 2012).18 (link) Briefly, isolated BMVECs, pericytes and astrocytes were trypsinized and resuspended in BD Pharmingen™ Stain Buffer (FBS). Cells were incubated with the antibodies against the surface markers CD31 (1:100, Invitrogen, RM5201) and PDGFR-β (1:100, Invitrogen,14-1402-82). For intracellular staining, a GFAP specific antibody (1:100, abcam, ab7260) was used to label astrocytes. Intracellular staining was performed using the BD Cytofix/Cytoperm™ Fixation and Permeabilization Solution (554722). Nonspecific background staining was assessed by appropriate fluorochrome-matched isotype antibodies. A BD FACSAria flow cytometer (version 6.1) was used to analyzed cell staining.
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