Arp2 depletion inhibits sheet-like protrusions but not linear protrusions of fibroblasts and lymphocytes - PubMed (original) (raw)

Arp2 depletion inhibits sheet-like protrusions but not linear protrusions of fibroblasts and lymphocytes

Susan M Nicholson-Dykstra et al. Cell Motil Cytoskeleton. 2008 Nov.

Abstract

The Arp2/3 complex-mediated assembly and protrusion of a branched actin network at the leading edge occurs during cell migration, although some studies suggest it is not essential. In order to test the role of Arp2/3 complex in leading edge protrusion, Swiss 3T3 fibroblasts and Jurkat T cells were depleted of Arp2 and evaluated for defects in cell morphology and spreading efficiency. Arp2-depleted fibroblasts exhibit severe defects in formation of sheet-like protrusions at early time points of cell spreading, with sheet-like protrusions limited to regions along the length of linear protrusions. However, Arp2-depleted cells are able to spread fully after extended times. Similarly, Arp2-depleted Jurkat T lymphocytes exhibit defects in spreading on anti-CD3. Interphase Jurkats in suspension are covered with large ruffle structures, whereas mitotic Jurkats are covered by finger-like linear protrusions. Arp2-depleted Jurkats exhibit defects in ruffle assembly but not in assembly of mitotic linear protrusions. Similarly, Arp2-depletion has no effect on the highly dynamic linear protrusion of another suspended lymphocyte line. We conclude that Arp2/3 complex plays a significant role in assembly of sheet-like protrusions, especially during early stages of cell spreading, but is not required for assembly of a variety of linear actin-based protrusions.

(c) 2008 Wiley-Liss, Inc.

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Figures

Figure 1

Figure 1. Arp2 suppression in 3T3 Fibroblasts

(A) Western blot of Arp2 (upper) and actin (lower) levels in Control and Arp2-knockdown whole cell extracts. (B) Phase and immunofluorescent images depicting Control (upper) and Arp2-KD (lower) cell stained for Arp2 to demonstrate depletion of endogenous Arp2 in GFP+ anti-Arp2-shRNA transfected cells. (C–D) Phase (left) and fluorescent images of polymerized actin (center) and GFP (right) in Control (C) and Arp2-KD (D) cells 78 hours post-transfection. Cells were plated onto glass coverslips immediately after transfection. (E–F) Phase contrast images of Control (E) and Arp2-KD (F) cells plated onto glass coverslips directly after transfection, then observed 78 hours post transfection by live cell imaging to monitor peripheral protrusion dynamics. (G–H) Enlarged phase contrast time lapse image of regions from Control (G) and Arp2-KD (H) depicted by boxes in D,E. Time points indicate time in minutes during time course. Bar: B,C = 20 μm; D–G = 10 μm.

Figure 2

Figure 2. Fibroblast Spreading Assay

SEM (A–C) and immunofluorescent (D–F) staining of 3T3s replated after trypsinization on PLL-coated coverslips and fixed after 20 min (A, D), 60 min (B, E) or 24 hours (C, F). SEM images taken at 500x, bar = 50μm. D–F) Phase (left), polymerized actin (middle) and tubulin (right) staining. Polymerized actin labeled with rhodamine-phalloidin. Image levels adjusted independently to reflect localization and organization of polymerized actin and tubulin. (G,H) Fluorescent time-lapse images of 3T3s expressing 6His-GFP-Actin (G) or GFP-Arp3 (H) during replating time course on PLL-coated coverslips. Bar: D–F = 20 μm, G,H = 10 μm.

Figure 3

Figure 3. Spreading time course of Arp2-knockdown 3T3 fibroblasts on PLL

Images of phase and fluorescently stained F-Actin and tubulin in Empty Vector Control (A) and Arp2-knockdown cells after 20 min, 60 min, 120 min and 8 hours after trypsinization and replating on PLL-coated coverslips. Fluorescent levels separately adjusted to optimize view of F-actin and tubulin in each image. Bar: A–B = 10 μm. (C) Quantification of morphology of Empty Vector Control and Arp2-knockdown cells after 20 minutes of spreading on PLL-coated coverslips. (D) Quantification of number of Empty Vector Control and Arp2-knockdown cells adhered to coverslip and exhibiting a spread morphology similar to untransfected control cells (see Fig. 1).

Figure 4

Figure 4. Arp2-knockdown inhibits cell spreading and lamellipodial protrusion

(A–I) Phase contrast time lapse images of cells spreading on PLL-coated coverslips. (A) Untransfected control (A) and Arp2-knockdown (B) cells observed from 30–46 minutes after initiation of spreading assay. (C–E) Enlarged inset of peripheral lamellipodial protrusions (C) of control cell outlined in (A) and of lamellipodia-like protrusion along the length of pre-existing filopodia-like protrusions of Arp2-knockdown cells (D, solid box; E, hashed box) outlined in (B). Empty Vector Control (F) and Arp2-knockdown (G) cells observed 30–38 minutes after initiation of spreading assay. Enlarged inset of peripheral lamellipodial protrusions of control cell (H) outlined in (F) and of remaining lamellipodial protrusions of Arp2-knockdown cell (I) outlined in (G). Bar: A,B = 10μm; C–E = 5 μm; F,G = 10μm; H,I = 2 μm.

Figure 5

Figure 5. Arp2-depletion inhibits Jurkat ruffle formation

SEM (A) and fluorescent images of actin-rich ruffles (B) on the surface of Jurkat cells in suspension. SEM images of Control (C) and Arp2-KD (D) cells fixed in suspension 76–78 hours post-transfection. Bars: A–E = 2 μm. Cells were evaluated for the presence of ruffles, microvilli, blebs and bald surfaces (E).

Figure 6

Figure 6. The microvilli of Arp2-depleted Jurkats are not a result of mitotic arrest

SEM (A) and fluorescent (B) images of untransfected Jurkat cells demonstrating presence of occasional microvillar-covered cells, clearly seen by low-magnification SEM images (A) and by imaging the apical surface of cells stained for polymerized actin (B). Microvilli-covered cells are outlined by boxes. (C,D) SEM (upper) and immunfluorescent images (lower) of Untreated Control cells (C) and Nocodazole-blocked cells 45 minutes post-washout (D). Fluorescent images include rhodamine-phalloidin stained actin on dorsal surface (upper), anti-tubulin stained microtubules (middle) and DAPI-stained DNA (lower). (E) Quantification of surface morphology (by SEM analysis) of untreated and post-nocodazole washout cells. Cells were evaluated for presence of ruffles, microvilli, blebs or bald surfaces. (F) Mitotic Index of control and 45 min post-nocodazole washout cells. Immunofluorescent images were evaluated for total number of interphase and mitotic cells in general population. (G) Mitotic Index of Control and Arp2-depleted cells 76 hours after transfection. Quantification presented in F,G is from a single experiment that is representative of multiple nocodazole block and release trials.

Figure 7

Figure 7. Arp2-depletion has no effect on microvillar formation in 300.19 cells

Western blot analysis of Control and Arp2-KD 300.19 cells (A) stained with anti-Arp2. (B,C) Phase (left) and fluorescent images of the actin-rich puncta and the peripheral band of actin of GFP+ Control (B) and Arp2-KD (C) cells. SEM images of Control (D) and Arp2-KD (E) cells fixed in suspension. Bar: B–E = 5 μm.

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