Myeloid progenitors in the bone marrow differentiate into most of the major cell types of the immune system, including macrophages and dendritic cells. These cells play important roles in both innate and adaptive immunity. They express a number of proteases and protease inhibitors including members of the serine proteinase inhibitor or serpin superfamily. In this study we report the differential expression of neuroserpin in cells of the human myeloid lineage. Neuroserpin was highly expressed and secreted following the differentiation of monocytes to macrophages and dendritic cells. Activation of dendritic cells with lipo-polysaccharide resulted in increased neuroserpin mRNA levels but no neuroserpin secretion. Confocal immunofluorescence microscopy showed neuroserpin was differentially localised in human myeloid cells. In macrophages and dendritic cells it was concentrated in vesicles located in close proximity to the plasma membrane. The majority of activated dendritic cells also exhibited an intracellular focal concentration of neuroserpin which co-localised with the lysosomal/late endosomal marker LAMP-I. As neuroserpin inhibits tissue plasminogen activator, a comparative analysis of tPA and plasminogen activator inhibitor-I (PAI-1) expression was undertaken. This analysis revealed differential expression of PAI-I and neuroserpin suggesting they may have different functions in human immune cells.

Expression of the serine protease inhibitor neuroserpin in cells of the human myeloid lineage / Sarah A., Kennedy; Angela C., Van Diepen; Cecilia M., Van Den Hurk; Leigh C., Coates; Tet Woo, Lee; Lena L., Ostrovsky; MIRANDA BANOS, MARIA ELENA; Juan, Perez; Mark J., Davies; David A., Lomas; P., Rod Dunbar; Nigel P., Birch. - In: THROMBOSIS AND HAEMOSTASIS. - ISSN 0340-6245. - 97:3(2007), pp. 394-399. [10.1160/th06-09-0543]

Expression of the serine protease inhibitor neuroserpin in cells of the human myeloid lineage

MIRANDA BANOS, MARIA ELENA;
2007

Abstract

Myeloid progenitors in the bone marrow differentiate into most of the major cell types of the immune system, including macrophages and dendritic cells. These cells play important roles in both innate and adaptive immunity. They express a number of proteases and protease inhibitors including members of the serine proteinase inhibitor or serpin superfamily. In this study we report the differential expression of neuroserpin in cells of the human myeloid lineage. Neuroserpin was highly expressed and secreted following the differentiation of monocytes to macrophages and dendritic cells. Activation of dendritic cells with lipo-polysaccharide resulted in increased neuroserpin mRNA levels but no neuroserpin secretion. Confocal immunofluorescence microscopy showed neuroserpin was differentially localised in human myeloid cells. In macrophages and dendritic cells it was concentrated in vesicles located in close proximity to the plasma membrane. The majority of activated dendritic cells also exhibited an intracellular focal concentration of neuroserpin which co-localised with the lysosomal/late endosomal marker LAMP-I. As neuroserpin inhibits tissue plasminogen activator, a comparative analysis of tPA and plasminogen activator inhibitor-I (PAI-1) expression was undertaken. This analysis revealed differential expression of PAI-I and neuroserpin suggesting they may have different functions in human immune cells.
2007
dendritic cells; macrophages; monocytes; serpin; tissue plasminogen activator
01 Pubblicazione su rivista::01a Articolo in rivista
Expression of the serine protease inhibitor neuroserpin in cells of the human myeloid lineage / Sarah A., Kennedy; Angela C., Van Diepen; Cecilia M., Van Den Hurk; Leigh C., Coates; Tet Woo, Lee; Lena L., Ostrovsky; MIRANDA BANOS, MARIA ELENA; Juan, Perez; Mark J., Davies; David A., Lomas; P., Rod Dunbar; Nigel P., Birch. - In: THROMBOSIS AND HAEMOSTASIS. - ISSN 0340-6245. - 97:3(2007), pp. 394-399. [10.1160/th06-09-0543]
File allegati a questo prodotto
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/141132
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 10
  • Scopus 20
  • ???jsp.display-item.citation.isi??? 20
social impact