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PKCδ Clustering at the Leading Edge and Mediating Growth Factor-Enhanced, but not ECM-Initiated, Dermal Fibroblast Migration  Jianhua Fan, Shengxi Guan,

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Presentation on theme: "PKCδ Clustering at the Leading Edge and Mediating Growth Factor-Enhanced, but not ECM-Initiated, Dermal Fibroblast Migration  Jianhua Fan, Shengxi Guan,"— Presentation transcript:

1 PKCδ Clustering at the Leading Edge and Mediating Growth Factor-Enhanced, but not ECM-Initiated, Dermal Fibroblast Migration  Jianhua Fan, Shengxi Guan, Chieh-Fang Cheng, Michele Cho, Joshua W. Fields, Mei Chen, Mitchell F. Denning, David T. Woodley, Wei Li  Journal of Investigative Dermatology  Volume 126, Issue 6, Pages (June 2006) DOI: /sj.jid Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

2 Figure 1 DF expresses multiple isoforms of the PKC family kinases. (a–k) Equal amounts of total cell lysates of the indicated cell types, which were serum-starved overnight, were resolved in duplicates in SDS-PAGEs, transferred to nitrocellulose membranes and immunoblotted with a panel of antibodies specifically against PKC isoforms. A duplicate membrane was blotted with anti-p38 MAPK antibody as sample loading control. This experiment was repeated twice and similar results were obtained. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

3 Figure 2 PDGF-BB strongly stimulates membrane clustering of PKCδ at the leading edge of DFs. (a–r) DFs, cultured in collagen-pre-coated coverslip chambers and serum-starved overnight, were treated without or with PDGF-BB (15ng/ml) or PMA (100nm) for 15minutes, in which maximum translocation of PKCδ was detected. The cells were fixed, permeabilized, and immunostained with antibodies specifically against each of the six DAG-sensitive PKC isoforms expressed in DFs. Eight to 120 randomly selected cells by each antibody staining were analyzed. The percentages of the cells that represent the images were estimated and shown. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

4 Figure 3 An early and transient event of PDGF-BB-stimulated membrane translocation and leading edge clustering of PKCδ. (a–d) DFs, cultured in collagen-pre-coated coverslip chambers and serum-starved overnight, were untreated or treated with PDGF-BB (15ng/ml, the optimal concentration for cell migration) for the indicated time. Cells were fixed, permeabilized, and immunostained with anti-PKCδ antibody. The localization of the bound anti-PKCδ antibodies were indicated by a GFP-conjugated secondary antibody and visualized under a fluorescent microscope. Randomly selected 80–120 cells under each condition were analyzed and the percentages of the cells that represent the displayed images were shown. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

5 Figure 4 Requirement of the PKCδ kinase function for sustained membrane accumulation of PKCδ. (a–j) To study the role of its kinase domain, GFP-PKCδ-wt and GFP-PKCδ-KD fusion genes were constructed and cloned into lentiviral vector, pRRLsin-MCS-Deco. DFs, infected with GFP-PKCδ-wt or GFP-PKCδ-KD, were untreated or treated with PDGF-BB (15ng/ml) for the indicated time, fixed, and directly analyzed under fluorescent microscope. Randomly selected 80–120 cells under each condition were analyzed. The percentages of the cells that represent the images shown were estimated. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

6 Figure 5 PKCδ plays a critical role in PDGF-BB-stimulated, but not collagen-initiated, DF migration in vitro kinase assay. (a–l) DFs with overexpressed PKCδ-KD and DFs with downregulated PKCδ by siRNA were subjected to in vitro wound-healing assays, under three defined conditions: (1) ECM free and GF free (−/−); (2) collagen coating and GF free (+/−); and (3) collagen and PDGF-BB (+/+). All experiments were stopped in 16hours and wound closure analyzed. The wound closures were photographed and the quantitation (average gap, or AG) was carried out as described (Li et al., 2004b). The results shown here are reproducible in three independent experiments. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

7 Figure 6 PKCδ plays a critical role in PDGF-BB-stimulated, but not collagen-initiated, DF migration in colloidal gold migration assay. DFs, in which PKCδ signaling was blocked by either siRNA downregulation of the endogenous PKCδ or exogenously overexpression of PKCδ-KD, were subjected to colloidal gold migration in assays under three defined conditions: (1) ECM free and GF free (“control”); (2) collagen coating and GF free (“collagen”); and (3) collagen and PDGF-BB (“collagen+PDGF”). The cell migration in all experiments was stopped in 16hours and analyzed. (a–i, j) DFs with downregulated PKCδ by siRNA on colloidal gold migration assays and quantitation (migration index). (k–y, z) DF-overexpressing PKCδ-KD or MEK1-KD in colloidal gold migration assays and quantitation (migration Index). (aa–ff and gg) DF-overexpressing constitutively activated PKCδ-R144/145A in colloidal gold migration assays and quantitation (migration index). Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

8 Figure 7 PKCδ is not a direct activator of the three major MAPK cascades. Three approaches were used to interrupt PKCδ signaling, overexpression of PKCδ-KD mutant, downregulation of the endogenous PKCδ by PKCδ-siRNA, and overexpression of constitutively activated PKCδ-R144/145A mutant. (a, b) Western blot of the DF-expressing vector, PKCδ-wt, or PKCδ-KD. The lower part of the same membrane was blotted with anti-p38 antibody. (c–h) Lysates of DFs, overexpressing vector control, PKCδ-wt, or PKCδ-KD, were equalized and resolved in SDS-PAGEs. Duplicate gels were analyzed by Western immunoblotting analyses using antibodies specifically against the phosphorylated forms of (panel c) p38, (panel e) ERK1/2, and (panel g) JNK, or (panels d, f, and h, respectively) their peptides. This experiment was repeated multiple times. (i, j) Downregulation of the endogenous PKCδ protein by FG12 infection with siRNA against PKCδ, as shown by a Western blot. (k, l) PDGF-BB-stimulated p38 phosphorylation was analyzed in DF-expressing siRNA against PKCδ or vector and Lac-Z-siRNA controls. (m, n) DFs, expressing vector control, PKCδ-KD, or PKCδ-siRNA, were lysed by lysis buffer for in vitro kinase assay supplied by the manufacturer. p38 was immunoprecipitated by anti-p38 antibodies linked to argarose beads. (panel m) The immune complexes were then subjected to in vitro kinase assay using purified ATF-2 as the substrate. Phosphorylation of ATF-2 was used as the readout and quantitated by scanning densitometry. (panel n) The immunoprecipitation was monitored by blotting the membrane with an anti-p38 antibody. (o-r) Lysates of DFs, overexpressing PKCδ-wt or PKCδ-R144/145A, were analyzed by Western immunoblotting analyses using antibodies specifically against the phosphorylated forms of (panel o) p38, (panel p) ERK1/2 and (panel q) JNK, or (panel r) β-actin, respectively. (s–v) Lysates of DFs, either treated with increasing concentrations of rottlerin or overexpressing vector control, PKCδ-wt, or PKCδ-R144/145A and being treated with PDGF-BB (50ng/ml) for the indicated time, were equalized and resolved in SDS-PAGEs. Duplicate gels were analyzed by Western immunoblotting analyses using antibodies specifically against the phosphorylated forms of (panels s and u) Stat3, or (panels t and v) their peptides. These experiments were repeated multiple times and similar results were obtained. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

9 Figure 8 A schematic working model for PKCδ signaling in DF migration during wound healing. The cells on collagen in the absence of PDGF do not undergo polarization and PKCδ does not translocate to the membrane. PDGF stimulation causes the PDGF receptor to dimerize and PKCδ to cluster at the leading edge of polarized cells. The membrane-bound PKCδ mediates PDGF-stimulated migration signals. However, PKCδ does not relay the motility signal to any of the three major MAPK cascades. Instead, it appears to act upstream of Stat3, a critical factor in skin cell migration and wound healing (Sano et al., 1999). The relative numbers and proportions of the signaling molecules shown do not quantitatively reflect them in the cells. Journal of Investigative Dermatology  , DOI: ( /sj.jid ) Copyright © 2006 The Society for Investigative Dermatology, Inc Terms and Conditions

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