Acidic and neutral sialidases (pH optimum 4.7 and 7.2, respectively) were assayed on human circulating erythrocytes during ageing. The assays were performed on intact erythrocytes and resealed erythrocyte ghost membranes. From young to senescent erythrocytes the acidic sialidase featured a 2.7-fold and 2.5-fold decrease in specific activity when measured on intact cells or resealed ghost membranes, whereas the neutral sialidase a 5-fold and 7-fold increase, respectively. The Ca2+-loading procedure was employed to mimic the vesiculation process occurring during erythrocyte ageing. Under these conditions the released vesicles displayed an elevated content of acidic sialidase, almost completely linked through a glycan phosphoinositide (GPI) anchor but no neutral sialidase activity, that was completely retained by remnant erythrocytes together with almost all the starting content of sialoglycoconjugates. The loss with vesiculation of acidic sialidase with a concomitant relative increase of neutral sialidase was more marked in young than senescent erythrocytes. The data presented suggest that during ageing erythrocytes loose acidic sialidase, and get enriched in the neutral enzyme, the vesiculation process, possibly involving GPI-anchors-rich membrane microdomains, being likely responsible for these changes. The enhanced neutral sialidase activity might account for the sialic acid loss occurring during erythrocyte ageing.

Different behaviour of ghost-linked acidic and neutral sialidases during human erythrocyte ageing / C. Tringali, A. Fiorilli, B. Venerando, G. Tettamanti. - In: GLYCOCONJUGATE JOURNAL. - ISSN 0282-0080. - 18:5(2001 May), pp. 407-418.

Different behaviour of ghost-linked acidic and neutral sialidases during human erythrocyte ageing

C. Tringali
Primo
;
A. Fiorilli
Secondo
;
B. Venerando
Penultimo
;
G. Tettamanti
Ultimo
2001

Abstract

Acidic and neutral sialidases (pH optimum 4.7 and 7.2, respectively) were assayed on human circulating erythrocytes during ageing. The assays were performed on intact erythrocytes and resealed erythrocyte ghost membranes. From young to senescent erythrocytes the acidic sialidase featured a 2.7-fold and 2.5-fold decrease in specific activity when measured on intact cells or resealed ghost membranes, whereas the neutral sialidase a 5-fold and 7-fold increase, respectively. The Ca2+-loading procedure was employed to mimic the vesiculation process occurring during erythrocyte ageing. Under these conditions the released vesicles displayed an elevated content of acidic sialidase, almost completely linked through a glycan phosphoinositide (GPI) anchor but no neutral sialidase activity, that was completely retained by remnant erythrocytes together with almost all the starting content of sialoglycoconjugates. The loss with vesiculation of acidic sialidase with a concomitant relative increase of neutral sialidase was more marked in young than senescent erythrocytes. The data presented suggest that during ageing erythrocytes loose acidic sialidase, and get enriched in the neutral enzyme, the vesiculation process, possibly involving GPI-anchors-rich membrane microdomains, being likely responsible for these changes. The enhanced neutral sialidase activity might account for the sialic acid loss occurring during erythrocyte ageing.
English
Blood cells; Glycoconjugates; Glycohydrolases; Human biochemistry; Plasma membranes
Settore BIO/10 - Biochimica
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
Articolo
Sì, ma tipo non specificato
mag-2001
Springer Netherlands
18
5
407
418
Periodico con rilevanza internazionale
http://www.springerlink.com/content/k423t88426p0u117/
info:eu-repo/semantics/article
Different behaviour of ghost-linked acidic and neutral sialidases during human erythrocyte ageing / C. Tringali, A. Fiorilli, B. Venerando, G. Tettamanti. - In: GLYCOCONJUGATE JOURNAL. - ISSN 0282-0080. - 18:5(2001 May), pp. 407-418.
none
Prodotti della ricerca::01 - Articolo su periodico
4
262
Article (author)
si
C. Tringali, A. Fiorilli, B. Venerando, G. Tettamanti
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/26242
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