دورية أكاديمية

Binding and migration across fibronectin and VCAM-1 of cycling hematopoietic progenitor cells.

التفاصيل البيبلوغرافية
العنوان: Binding and migration across fibronectin and VCAM-1 of cycling hematopoietic progenitor cells.
المؤلفون: Gothot A; National Fund for Scientific Research, Brussels and University of Liège, Liège, Belgium. agothot@ulg.ac.be, Giet O, Huygen S, Beguin Y
المصدر: Leukemia & lymphoma [Leuk Lymphoma] 2003 Aug; Vol. 44 (8), pp. 1379-83.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Review
اللغة: English
بيانات الدورية: Publisher: Taylor & Francis Country of Publication: United States NLM ID: 9007422 Publication Model: Print Cited Medium: Print ISSN: 1042-8194 (Print) Linking ISSN: 10268022 NLM ISO Abbreviation: Leuk Lymphoma Subsets: MEDLINE
أسماء مطبوعة: Publication: [Philadelphia, PA] : Taylor & Francis
Original Publication: Chur ; New York : London, UK : Harwood Academic Publishers ; Distributed by STBS, 1989-
مواضيع طبية MeSH: Fibronectins/*metabolism , Hematopoietic Stem Cells/*cytology , Vascular Cell Adhesion Molecule-1/*metabolism, Animals ; Cell Adhesion ; Cell Movement ; Graft Survival ; Hematopoiesis ; Hematopoietic Stem Cell Transplantation ; Hematopoietic Stem Cells/physiology ; Humans
مستخلص: Using different experimental approaches, it has been established that transplantability of hematopoietic/stem progenitor cells is ineffective during transit through the cell cycle. Although primitive stem cells are responsive to mitogenic stimulation in optimized ex vivo conditions, defective engraftment of generated cells may limit their detection in standard transplantation models as well as their use in clinical cell therapy. The activation level of adhesion receptors is modulated by stimulation of cytokine receptors via "inside-out" signaling. This prompted us to study the interactions of progenitor cells with fibronectin (Fn) in different phases of the cell cycle. We first demonstrated that adhesion to Fn was stimulated in S/G2 + M as compared to G0/G1, in ex vivo cultured CD34+ cells, with a predominant usage of very late antigen (VLA)-5 over that of VLA-4. We next determined that maximal Fn binding in active phases of the cell cycle limited cell motility toward stromal cell-conditioned medium. It was also observed that VLA-4 and VLA-5 ability to mediate adhesion or migration varied independently during cell cycle transit. Finally, in synchronized progenitor cells executing a first cell cycle ex vivo, a reversible increase in Fn binding was associated with a reversible decrease in adhesion to vascular cell-adhesion molecule (VCAM)-1. Overall, these observations suggest that defective engraftment of cycling stem/progenitor cells may result, at least in part, from abnormal trafficking related to changes in the activation level of adhesion receptors.
Number of References: 34
التعليقات: Erratum in: Leuk Lymphoma. 2003 Oct;44(10):following 1839.
المشرفين على المادة: 0 (Fibronectins)
0 (Vascular Cell Adhesion Molecule-1)
تواريخ الأحداث: Date Created: 20030904 Date Completed: 20040316 Latest Revision: 20191107
رمز التحديث: 20240628
DOI: 10.1080/1042819031000083406
PMID: 12952232
قاعدة البيانات: MEDLINE
الوصف
تدمد:1042-8194
DOI:10.1080/1042819031000083406