دورية أكاديمية

Cell adhesion dynamics and actin cytoskeleton reorganization in HepG2 cell aggregates.

التفاصيل البيبلوغرافية
العنوان: Cell adhesion dynamics and actin cytoskeleton reorganization in HepG2 cell aggregates.
المؤلفون: Edwards GO; Cardiff School of Biosciences, Main Building, Cardiff University, Cardiff, Wales, UK. edwardsgo@cardiff.ac.uk, Bazou D, Kuznetsova LA, Coakley WT
المصدر: Cell communication & adhesion [Cell Commun Adhes] 2007 Jan-Feb; Vol. 14 (1), pp. 9-20.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Taylor & Francis Country of Publication: England NLM ID: 101096596 Publication Model: Print Cited Medium: Print ISSN: 1541-9061 (Print) Linking ISSN: 15435180 NLM ISO Abbreviation: Cell Commun Adhes Subsets: MEDLINE
أسماء مطبوعة: Publication: [London] : Taylor & Francis
Original Publication: Basingstoke, Hants, UK : Harwood Academic Publishers, c2001-
مواضيع طبية MeSH: Actins/*metabolism , Cytoskeleton/*metabolism, Cell Adhesion ; Cell Aggregation ; Cell Death ; Cell Line, Tumor ; Cell Shape ; Cellular Senescence ; Cytoskeleton/chemistry ; Humans ; Microscopy, Fluorescence ; Protein Transport ; Ultrasonics
مستخلص: The temporal dependence of cytoskeletal remodelling on cell-cell contact in HepG2 cells has been established here. Cell-cell contact occurred in an ultrasound standing wave trap designed to form and levitate a 2-D cell aggregate, allowing intercellular adhesive interactions to proceed, free from the influences of solid substrata. Membrane spreading at the point of contact and change in cell circularity reached 50% of their final values within 2.2 min of contact. Junctional F-actin increased at the interface but lagged behind membrane spreading, reaching 50% of its final value in 4.4 min. Aggregates had good mechanical stability after 15 min in the trap. The implication of this temporal dependence on the sequential progress of adhesion processes is discussed. These results provide insight into how biomimetic cell aggregates with some liver cell functions might be assembled in a systematic, controlled manner in a 3-D ultrasound trap.
المشرفين على المادة: 0 (Actins)
تواريخ الأحداث: Date Created: 20070425 Date Completed: 20071019 Latest Revision: 20171116
رمز التحديث: 20231215
DOI: 10.1080/15419060701224849
PMID: 17453827
قاعدة البيانات: MEDLINE
الوصف
تدمد:1541-9061
DOI:10.1080/15419060701224849