TY - JOUR
T1 - Tomato lectin histochemistry for microglial visualization
AU - Villacampa, Nàdia
AU - Almolda, Beatriz
AU - González, Berta
AU - Castellano, Bernardo
PY - 2013/7/18
Y1 - 2013/7/18
N2 - The use of different lectins for the study of microglial cells in the central nervous system (CNS) is a valuable tool that has been extensively used in the last years for the selective staining of this glial cell population, not only in normal physiological conditions, but also in a wide range of pathological situations where the normal homeostasis of the parenchyma is disturbed. In this chapter we accurately describe the methodology for the selective labelling of microglial cells by using the tomato lectin (TL), a protein lectin obtained from Lycopersicum esculentum with specific affinity for poly-N-acetyl lactosamine sugar residues which are found on the plasma membrane and in the cytoplasm of microglia. Here we describe how to perform this technique on vibratome, frozen, and paraffin sections for optical microscopy, as well as for transmission electron microscopy (TEM) studies. Using this methodology it is possible to visualize amoeboid microglia in the developing brain, ramified microglia in the adult, and activated/reactive microglia in the experimentally damaged brain. In addition, as TL also recognized sugar residues in endothelial cells, this technique is very useful for the study of the relationship established between microglia and the CNS vasculature. © 2013 Springer Science+Business Media New York.
AB - The use of different lectins for the study of microglial cells in the central nervous system (CNS) is a valuable tool that has been extensively used in the last years for the selective staining of this glial cell population, not only in normal physiological conditions, but also in a wide range of pathological situations where the normal homeostasis of the parenchyma is disturbed. In this chapter we accurately describe the methodology for the selective labelling of microglial cells by using the tomato lectin (TL), a protein lectin obtained from Lycopersicum esculentum with specific affinity for poly-N-acetyl lactosamine sugar residues which are found on the plasma membrane and in the cytoplasm of microglia. Here we describe how to perform this technique on vibratome, frozen, and paraffin sections for optical microscopy, as well as for transmission electron microscopy (TEM) studies. Using this methodology it is possible to visualize amoeboid microglia in the developing brain, ramified microglia in the adult, and activated/reactive microglia in the experimentally damaged brain. In addition, as TL also recognized sugar residues in endothelial cells, this technique is very useful for the study of the relationship established between microglia and the CNS vasculature. © 2013 Springer Science+Business Media New York.
KW - Double labelling
KW - Fluorescence
KW - Histochemistry
KW - Microglia
KW - Tomato lectin
KW - Transmission electron microscopy
UR - https://www.scopus.com/pages/publications/84880122334
U2 - 10.1007/978-1-62703-520-0_23
DO - 10.1007/978-1-62703-520-0_23
M3 - Article
SN - 1064-3745
VL - 1041
SP - 261
EP - 279
JO - Methods in Molecular Biology
JF - Methods in Molecular Biology
ER -