“…Microglial cells are derived from the monocyte/macrophage lineage, and they progressively enter the nervous system during development (Cuadros and Navascues, 1998). Nondifferentiated microglial cells thus label with typical macrophage markers, such as lectins (Acarin et al, 1994;Andjelkovic et al, 1998) or different phagocyte antibodies (Kullberg et al, 2001;Choi et al, 2004;Herber et al, 2006). In agreement with our results, in most of these cases the intensity of the staining with different markers greatly diminishes as the microglia ramify.…”
Section: Cathepsin B and D Expression In Macrophages And Microglial Psupporting
Here, we show a detailed chronotopographical analysis of cathepsin B and D expression during development of the mouse visual system. Both proteases were detected in large rounded/ameboid cells usually located in close relationship with prominent sites of extensive physiological cell death. In concordance with their morphological features and topographical distribution, we demonstrate that expressing cells corresponded with macrophages and microglial precursors. We found that as microglial precursors differentiated the expression of both cathepsins was down-regulated. Of interest, cathepsin B and D transcripts were never observed in degenerating cells. Our findings point to a role for cathepsin D and B in cell debris degradation after apoptotic processes rather than promoting cell death, as proposed for other developmental models. Additionally their pattern of expression suggests a role in the maturation of the microglial precursors.
“…Microglial cells are derived from the monocyte/macrophage lineage, and they progressively enter the nervous system during development (Cuadros and Navascues, 1998). Nondifferentiated microglial cells thus label with typical macrophage markers, such as lectins (Acarin et al, 1994;Andjelkovic et al, 1998) or different phagocyte antibodies (Kullberg et al, 2001;Choi et al, 2004;Herber et al, 2006). In agreement with our results, in most of these cases the intensity of the staining with different markers greatly diminishes as the microglia ramify.…”
Section: Cathepsin B and D Expression In Macrophages And Microglial Psupporting
Here, we show a detailed chronotopographical analysis of cathepsin B and D expression during development of the mouse visual system. Both proteases were detected in large rounded/ameboid cells usually located in close relationship with prominent sites of extensive physiological cell death. In concordance with their morphological features and topographical distribution, we demonstrate that expressing cells corresponded with macrophages and microglial precursors. We found that as microglial precursors differentiated the expression of both cathepsins was down-regulated. Of interest, cathepsin B and D transcripts were never observed in degenerating cells. Our findings point to a role for cathepsin D and B in cell debris degradation after apoptotic processes rather than promoting cell death, as proposed for other developmental models. Additionally their pattern of expression suggests a role in the maturation of the microglial precursors.
“…66 -69 In contrast, perivascular macrophages appear later when the vasculature develops. 67,70 Previous studies in adult rodents have shown that macrophages in the perivascular, meningeal, and choroid plexus turnover regularly, whereas the repopulation of microglia by bone marrow precursors is limited, at least under normal conditions. 3,[71][72][73] Therefore, perivascular macrophages in adult and developing CNS are undoubtedly of monocytic origin.…”
Section: Cd163 a Monocyte Lineage Marker For Perivascular Macrophagesmentioning
“…Infiltration of monocytes could be confirmed by carbon-labelling (Ling et al, 1980) and histochemical studies using marker enzymes for monocytes (Ferrer and Sarmiento, 1980;Ling et al, 1982). Andjelkovic and colleagues labelled microglia in the developing and adult human brain using lectin-histochemistry (Andjelkovic et al, 1998). Lectin positive cells can be subdivided into two groups which both exist in the adult brain, but show different distribution and time schedule of morphological changes.…”
Section: Origin and Sources Of Microgliamentioning
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