Disruption of microfilaments alters laminin synthesis but not laminin trafficking in NHEK in vitro

• Published in: In vitro cellular & developmental biology. Animal Vol. 32; no. 5; p. 300
• Main Authors: Cook, J R, Van Buskirk, R G
• Format: Journal Article
• Language: English
• Published: Germany 01.05.1996
• Subjects: Actin Cytoskeleton - drug effects; Actin Cytoskeleton - physiology; Cells, Cultured; Cytochalasin D - pharmacology; Electrophoresis, Polyacrylamide Gel; Humans; Immunosorbent Techniques; Keratinocytes - metabolism; Keratinocytes - ultrastructure; Laminin - biosynthesis; Laminin - metabolism; Nocodazole - pharmacology
• ISSN: 1071-2690
• DOI: 10.1007/BF02723063

Laminin synthesis and deposition are concomitant with the development of a basal lamina between the human epidermis and the underlying dermis. One of the challenges in tissue engineering of human epidermal models is to develop substrates and conditions that encourage the development of a basement membrane. The purpose of this study was to determine if actin filaments and/or microtubules are involved in the synthesis/secretion of laminin by normal human epidermal keratinocytes (NHEK) in vitro. NHEK synthesize and secrete laminin subunits B1, B2, and M but little, if any, of laminin subunit A. Data indicate that disruption of microfilaments by the destabilizing agent, cytochalasin D, had no apparent effect on the relative synthesis rates of most cytosolic proteins as revealed by one-dimensional sodium dodecyl sulfate (SDS) gel electrophoresis. This drug, however, increased laminin B2 synthesis several fold over untreated controls. This enhanced synthetic rate was independent of the type of collagen matrix on which the NHEK were grown. Similar increases in synthesis of the M and B1 laminin chains were not observed. To determine if this increase in synthesis lead to increases in laminin B2 secretion, laminin B2 was immunoprecipitated from both the apical and basal domains of NHEK cells grown on microporous membranes. While more laminin B1, B2, and M were secreted basally than apically, an observation consistent with laminin's role in basal lamina formation, cytochalasin D had no apparent effect on either basal or apical laminin B2 secretion. Experiments with the microtubule destabilizer, nocodazole, showed no similar effects on laminin synthesis and/or secretion. We conclude that (a) disruption of the actin network in NHEK selectively increases the synthesis of laminin B2, (b) the secretion of laminin B2 from NHEK cells is not governed by either the microfilamentous cytoskeleton or the amount of laminin synthesized by NHEK, and (c) disruption of the microtubular network does not alter laminin synthesis or secretion.