Abstract
Mortalin (Mot) is a mitochondrial chaperone of the heat shock protein 70 family and it’s pro-proliferative and anti-apoptosis functions could be associated with keloid pathogenesis, and blocking of mortalin and its interaction with p53 might be a potential novel target for the treatment of keloid. Therefore, we generated mortalin-specific small hairpin (sh) RNAs (dE1-RGD/GFP/shMot) and introduced into keloid spheroids for examination of its apoptotic and anti-fibrotic effect. On keloid tissues, mortalin expression was higher than adjacent normal tissues and it’s protein expressions were activated keloid fibroblasts (KFs). After primary keloid spheroid were transduced with dE1-RGD/GFP/shMot for knockdown of mortalin, expression of type I, III collagen, fibronectin, and elastin was significantly reduced and transforming growth factor-β1, epidermal growth factor receptor (EGFR), Extracellular Signal-Regulated Kinases 1 and 2 (Erk 1/2), and Smad 2/3 complex protein expression were decreased. In addition, increased TUNEL activities and cytochrome C were observed. Further, for examine of mortalin and p53 interaction, we performed immunofluorescence analysis. Knockdown of mortalin relocated p53 to the cell nucleus in primary keloid spheroids by dE1-RGD/GFP/shMot transduction. These results support the utility of knockdown of mortalin to induce apoptosis and reduce ECMs expression in keloid spheroid, which may be highly beneficial in treating keloids.
Similar content being viewed by others
Introduction
Keloids are defined as benign skin tumors, and occurred when the normal tissue repair sequence becomes dysregulated and the result of a prolonged proliferative and a delayed remodeling phase1,2,3. It caused by excessive extracellular matrix accumulation resulting from an aberrant extracellular matrix protein synthesis and degradation. Increased cell proliferation and an imbalance between collagen synthesis and degradation, accounting for the progressive and hypertrophic nature of keloids, correlates with reduced apoptosis, which may explain keloid pathogenesis3,4,5,6,7. Overexpression of tumor suppressor protein p537,8,9 and mutation in the p53 gene8,9,10,11,12 had been found in keloids, and these may be linked to keloid pathogenesis. p53 is a nuclear transcription factor often found in cytosol which translocates to the nucleus in response to stress, ultimately promoting apoptosis of damaged cells3,6,13,14.
Mortalin (Mot; mtHsp70/PBP74/Grp75) is a 679 amino acids long (MW 73,913 Da) heat un-inducible member of Hsp70 family of proteins and plays an essential role in mitochondrial import, oxidative stress response, regulation of mitochondrial membrane potential, energy generation, intracellular transport, chaperonization, protection against apoptosis, and p53 functions15,16,17. Mortalin and p53 interactions were first identified in the cytoplasm of tumor cells. The pro-proliferative effects of mortalin overexpression in cancer cells have been assigned to its binding with p53 that results in its retention in the cytoplasm, and inhibition of its normal transcriptional activation function of p5316,18,19,20,21, resulting in lifespan extension of cells, uncontrolled proliferation, and malignant transformation. But in normal human cells, mortalin predominantly present in mitochondria where it mediates transcription-independent tumor suppression by induction of mitochondrial permeabilization and apoptosis22,23. Several other studies have assigned in line with an anti-apoptotic function to mortalin21,23,24,25,26. Anti-mortalin molecule, such as antisense, ribozyme, and shRNA that that abrogated mortalin-p53 interaction and caused the relocation of p53 to the cell nucleus, resulted in growth arrest/apoptosis of cancer cells19,26,27,28. However, the expression of mortalin and mortalin-p53 interaction on the keloid was not investigated.
Keloid scars are locally aggressive, continually grow, and invade the surrounding normal skin, and are caused by increased proliferation and an excess collagen deposition by abnormal fibroblasts. On the basis of these characteristics of keloid, we hypothesize that the pro-proliferative and anti-apoptosis functions of mortalin could be associated with keloid pathogenesis, and targeting mortalin and its interaction with p53 might be a potential novel target for the treatment of keloid. Therefore, in the present study, we investigate the expression of mortalin in keloid and normal tissues, where it protects cell apoptosis by mechanisms involving inactivation of p53 functions. Also, we generated mortalin-specific small hairpin (sh)RNAs (dE1-RGD/GFP/shMot) and introduced into keloid spheroids for examination of its apoptotic and anti-fibrotic effect.
Results
Mortalin expression was increased in keloid tissues compared with adjacent normal tissues
After hematoxylin and eosin (H&E) staining, we observed that keloid tissue had a dense and excessive collagen deposition that extended over the clinical keloid margin into the extra-lesional dermal tissue (Fig. 1a). To evaluate mortalin protein expression patterns in keloid tissue, immunohistochemical staining was performed (n = 5). Compared to extra-lesional normal tissue (Fig. 1b & e), markedly increased mortalin immunoreactivity was noted in central and peripheral keloid region (Fig. 1c & d). The increased expression of mortalin was semi-quantitatively measured with MetaMorph® image analysis software (Fig. 1f). The results showed that mortalin protein levels were markedly higher in the central and transitional regions of the keloids (optical density; 92446 ± 17322, 99007 ± 19811, respectively) than in normal tissue (optical density; 23005 ± 3969). Protein expression levels of mortalin in keloid tissues were 4.8 times that of normal tissue (**p < 0.01).
Mortalin protein expression was investigated with Western blot analysis (n = 3). As shown in Fig. 2, mortalin protein levels were 25 times higher in KFs relative to normal dermal tissue, which was further upregulated by 2.3-fold when KFs were activated with transforming growth factor (TGF)-β1 (10 ng/mL), a strong fibrosis inducing factor that plays an important role in the keloid pathophysiology.
Construction of mortalin specific shRNA-expressing adenovirus and their effect on the KFs and keloid spheroids
On the basis of the results that mortalin expression increased on the keloid tissues, we anticipated that inhibition of mortalin could be applied for keloid or hypertrophic scar treatment. Therefore, we generated mortalin-specific shRNA-expressing adenovirus (Fig. 3a) and examined their effect on KFs and keloid spheroids. As shown in Fig. 3b and c, overexpressed mortalin on the cytosolic and extracellular area of KFs (Fig. 3b) and primary keloid spheroid (Fig. 3c), which were examined by immunofluorescence assay, were extremely knockdown by the treatment of dE1-RGD/GFP/shMot.
Mortalin specific shRNA-expressing adenovirus decreases collagen type I and III, elastin, and fibronectin protein expression in primary human keloid spheroids
Keloid spheroids derived from active-stage keloid patients (n = 3) were cultured and transduced with either dE1-RGD/GFP/scramble or dEl-RGD/GFP/shMot. The effect of mortalin on expression of major ECM components of keloid was evaluated histologically. Masson’s trichrome of keloid sections revealed that collagen deposition was decreased in spheroids transduced with dEl-RGD/GFP/shMot versus scramble virus (Fig. 4a). In addition, dense and coarse collagen bundles structure were replaced by thin and shallow collagen bundles. Image analysis of immunohistochemical staining also revealed significantly reduced type I collagen, type III collagen, elastin, and fibronectin in dEl-RGD/GFP/shMot treated keloid spheroids, by 12%, 43%, 12%, and 18%, respectively, versus scramble virus-transduced spheroids (**p < 0.01 in all cases; Fig. 4b and c). Taken together, these data strongly suggest that expressions of the major ECM components such as collagen type I and III, elastin, and fibronectin are significantly decreased by knockdown of mortalin expression in primary keloid spheroid.
Mortalin specific shRNA-expressing adenovirus elicited decreased expression of TGF-β1, EGFR, and Erk 1/2 on keloid spheroids
We examined that dEl-RGD/GFP/shMot may be decreased expression of TGF-β1 and EGFR on keloid spheroid compared with dE1-RGD/GFP/scramble. Also, to examine the intracellular effect of mortalin specific shRNA-expressing adenovirus, Smad 2/3 complex and Erk 1/2 protein expressions were investigated. As shown in Fig. 4d, significantly decreased expressions of TGF-β1, EGFR, Smad 2/3 complex, and Erk 1/2 protein were observed in mortalin specific shRNA-expressing adenovirus treated keloid spheroids, by 52%, 43%, 11%, and 42%, respectively, versus scramble virus-transduced spheroids (*p < 0.05, **p < 0.01; Fig. 4d and e). These results demonstrated that knockdown of mortain can attenuate EGF/EGFR signaling pathway and TGF-β1/Smad pathway, which have an important role in the fibrogenesis. Also, overexpressed mortalin has an important role in keloid pathogenesis and inhibition of mortalin expression could be a therapeutic target on the treatment of keloid or hypertrophic scar.
Knockdown of mortalin decreased PCNA expression and induced apoptosis
Keloid formation is often considered to be the result of a prolonged cellular proliferation and reduced apoptosis. Therefore, proliferative activities of keloid was examined by a proliferating cell nuclear antigen (PCNA) immunohistochemical staining on keloid tissues (n = 5), resulted that expression of PCNA protein markedly increased in central and transitional keloid region compared to adjacent normal tissue by 3.9 times and 3.2 times, respectively (Fig. 5a and b). Next, we examined whether the knockdown of mortalin could decrease cellular proliferation and induce apoptosis in scramble and mortalin specific shRNA-expressing adenovirus-transfected keloid spheroid. Image analysis of immunohistochemical staining revealed significantly reduced PCNA expression in dEl-RGD/GFP/shMot treated keloid spheroids by 29% (Fig. 5c and d).
Further, to determine whether reduced mortalin expression induced apoptosis, a TUNEL assay and cytochrome C immune-staining were carried out using the keloid spheroid. As shown in Fig. 5c and d, TUNEL positivities were increased on the dEl-RGD/GFP/shMot-treated keloid spheroids, and expression of cytochrome C protein was increased by 1.8 times after dEl-RGD/GFP/shMot transduction. In addition, wild type p53, phospho-p53, p21, and caspase 3 were increased by 2.8-, 8.5-, 3.2-, and 5.7-fold, respectively, in primary keloid fibroblast after transduction with dE1-RGD/GFP/shMot (200 MOI) in comparison with dE1-RGD/GFP/scramble (200 MOI) group (Supplementary Fig. S2). Taken collectively, our results suggest that knockdown of mortalin protein decrease cell proliferation and induce apoptosis, and mortalin may be a target for keloid treatment.
Mortalin as p53 inactivator; Mortalin interacts with p53 and its knockdown relocate p53 to the cell nucleus in primary keloid spheroids
As shown in Fig. 6, overexpression of p53 protein on the KFs (Fig. 6a) and keloid tissues (n = 5) (Fig. 6b-c) were confirmed, and the localization of p53 was found in the cytoplasm as well as the nucleus, but most of them expressed in the cytoplasm. The cytoplasmic accumulation of p53 was especially noticeable on the keloid tissues. We next investigated whether mortalin would cause inactivation of p53 function by cytoplasmic sequestration. If so, apoptosis caused by mortalin knockdown would be expected to involve nuclear translocation of the p53 and induce an apoptosis by reactivation of p53. To test this hypothesis, we performed immunofluorescence analysis on keloid spheroid (n = 3). Transduction of dEl-RGD/GFP/shMot led to significant accumulation of p53 in the nucleus. As shown in Fig. 6d, colocalizations of p53 and mortalin in the cytosol were investigated on the untreated keloid spheroid. After mortalin specific shRNA-expressing adenovirus was treated on the keloid spheroids, mortalin expressions were knockdown and they was exhibited intense nuclear staining for p53, suggesting the nuclear translocation. In line with these findings, a time-dependent increase in nuclear p53 level was confirmed by western blot analysis in dEl-RGD/shMot-treated primary keloid fibroblast (Supplementary Fig. S3). In contrast, no nuclear p53 level was increased in scrambled shRNA-expressing Ad-treated cells.
Disscusion
Keloids are fibro-proliferative skin lesions that are characterized by excessive accumulation of ECM components–mainly collagens–and invasion into normal peripheral regions. Increased cell proliferation, accounting for the progressive and hypertrophic nature of keloids, correlates with a lower rate of apoptosis5,7,9, which may play a role in the process of pathological scarring. Therefore, apart from the researches keloid pathogenesis caused by increased proliferation and an excess collagen deposition by fibroblasts, the understanding of the mechanisms by which keloids escape from apoptosis could be beneficial in the development of novel therapeutic strategies.
Our data showed that mortalin and tumor suppressor protein p53 expression were increased on the keloid tissues compared with adjacent normal tissues, especially on the cytosol. In addition, mortalin expression significantly increased after TGF-β1 (10 ng/mL) treatment on keloid fibroblasts. Mortalin (mot-2/mthsp70/PBP74/GRP75) is an essential protein belonging to the Hsp70 family of chaperones, and its overexpression confers proliferation-growth advantages to cells15,16,18,20,21. Mortalin is primarily localized in the mitochondria but is also found in the endoplasmic reticulum, plasma membrane, and cytoplasmic vesicle29. It is also found as a secreted protein and detected in the extra-cellular space29. It protects cells from senescence and apoptosis and is overexpressed in cancer cells, but yet few report identified its role in fibrotic disease such as keloid. Therefore, we think that overexpressed mortalin in keloid tissue compared to the adjacent normal tissue could be an important role in fibrogenesis. In light of this, we generated mortalin-specific small hairpin (sh)RNAs (dE1-RGD/GFP/shMot) and introduced into keloid spheroids for examination of its apoptotic and anti-fibrotic effect. After the transduction of dE1-RGD/GFP/shMot, expressions of the major ECM components are significantly decreased in primary keloid spheroid, and knockdown of mortain can attenuate EGF/EGFR signaling pathway and TGF-β1/Smad pathway, which have a role in the fibrogenesis. The number of studies revealed that extracellular Hsp70 (Hsp 72) promotes TLR4 signaling leading to TGF-β1 activation30,31,32,33, and Hsp47 is a collagen-specific molecular chaperone that plays a critical role in normal procollagen biosynthesis in mammals34,35. However, the functional rule of mortalin for the fibrogenesis remains unclear. Therefore, additional researches will be needed.
The fibrotic process is maintained by the inhibition of apoptosis in myofibroblasts, which produce an excess of ECM, thereby causing keloid or hypertrophic scar. A number of nuclear proteins have been shown to redistribute to the cytosol and mitochondria at the onset of apoptosis. Among these, the tumor-suppressor protein p53 is a short lived nuclear phosphoprotein, which has transcription-dependent effects that involves induction of pro-apoptotic genes14,36,37 and overexpression of p537,8,9 had been found in keloids. In line with these reports, primary patient keloid fibroblast samples used in this study expressed wild type p53 (Supplementary Fig. S1).
The effects of overexpressed mortalin such as malignant transformation38, life span extension15, and attenuation of differentiation39 has been attributed, at least in part, to transcriptional inactivation of p53. There is well known that mortalin (amino-terminus region) was found to bind to the carboxy-terminus region of p53, resulting in cytoplasmic retention and transcriptional inactivation of p5316,18,19,20,21. Also, it localizes in the nucleus, inactivates p53-mediated apoptosis28. On the basis of theses knowledge, we blocked the cytosolic mortalin by dE1-RGD/GFP/shMot, and expected it to discharge p53 from mortalin–p53 complex resulting in its functional activation. As shown in our data, we examined that knockdown of mortalin induced nuclear translocation of the p53 and decrease cell proliferation. Also, apoptotic activity, cytochrome C release, and TUNEL positivities were increased on the dE1-RGD/GFP/shMot treated keloid spheroid.
On our researches, we found that functional roles of dE1-RGD/GFP/shMot such as anti-proliferative function, antifibrosis, and increase apoptotic activity could be expected to be of great advantage in keloid or hypertrophic scars therapeutics. Despite this role, the potential therapeutic use of shMot-expressing adenovirus possesses limitations, such as a transient effect, which is not desirable to chronically persistent keloids, acute inflammatory responses, and the innate immune response. Exhaustive research efforts has prompted the development of novel strategies to overcome these limitations40. Therefore, we think that further refinement studies will be needed for more efficient and safe gene transfer in patients.
Materials and Method
Human dermal fibroblast, keloid tissue, and keloid-derived fibroblast cells
Human normal dermal fibroblasts (HDFs) and keloid fibroblasts (KFs) were obtained from the ATCC (American Type Culture Collection, Manassas, VA). After obtaining informed consent according to a protocol approved by the Yonsei University College of Medicine Institutional Review Board, keloid tissues and normal abdominal skin tissues were obtained for fibroblast culture, histologic, and immunohistochemical analysis with excision. Keloid fibroblasts were obtained from both the central dermal layer of keloids (Supplementary Table 1). All experiments involving humans were performed in adherence to the Helsinki Guidelines. Cells were cultured in Dulbecco’s Modified Eagle’s Medium (DMEM; GIBCO, Grand Island, NY) supplemented with 10% heat-inactivated fetal bovine serum (FBS), penicillin (100 U/mL), streptomycin (100 μg/mL).
Immunohistochemistry (IHC) for mortalin, p53, and PCNA
Formaldehyde-fixed tissues were transferred to a paraffin-embedded block, sectioned at 4-μm thicknesses. After tissue deparaffinization and rehydration, endogenous peroxidase activity was blocked by 10-min incubation at room temperature with absolute methanol containing 1% hydrogen peroxide. The tissue sections were incubated with a primary antibody against mouse anti-mortalin monoclonal antibody (C1-3), rabbit anti-p53 (sc-6243; Santa Cruz biotechnology, Santa Cruz, CA), and mouse anti-PCNA (M0879; DAKO, Carpinteria, CA) at 4 °C overnight. After incubation with the secondary antibody (Super Sensitive™ Polymer-HRP IHC, BioGenex) for 1 h at room temperature, the bound complexes were visualized by incubating tissue sections with 0.05% diaminobenzidine and 0.003% hydrogen peroxide. The sections were counterstained with Harris hematoxylin and then dehydrated and mounted. Mortalin, p53, and PCNA protein levels were semi-quantitatively analyzed using MetaMorph® image analysis software (Universal Image Corp., Buckinghamshire, UK). Results are expressed as mean optical density of six different digital images per sample.
Generating shMot-expressing adenoviral vectors
A replication-incompetent Ad expressing shMot (dE1-RGD/GFP/shMot; Ad-shMot) and control Ad (dE1-RGD/GFP/scramble; Ad-scramble) were used in this study (Fig. 3). Both replication-incompetent Ads possess RGD, a tripeptide composed of L-arginine, glycine, and L-aspartic acid that recognizes subtypes of integrins, in their fiber to improve the transduction to keloid fibroblasts in comparison to wild-type Ad by providing an alternative viral entry pathway into keloid fibroblasts41,42. To generate an Ad expressing GFP and shMot or scramble at the E1 and E3 regions, respectively, pdE1-RGD/GFP43 was linearized by SpeI digestion and co-transformed into Escherichia coli BJ5183 with the XmnI-digested pSP72-E3/CMV-shMot or -scramble E3 shuttle vector44 for homologous recombination, generating a pdE1-RGD/GFP/shMot or /scramble adenoviral vector. The propagation, purification, and titration of Ad were performed as described previously45,46.
Preparation and adenoviral transduction of keloid spheroids
Keloid tissues were obtained from active-stage keloid patients (n = 5). Keloid spheroids were prepared by dissecting keloid central dermal tissue into 2-mm diameter pieces with sterile 21-gauge needles. Explants were plated onto HydroCell® 24 Multi-well plates (Nunc, Rochester, NY) after which they were cultured for 4 h in IMDM (Isocove’s modified Dulbecco’s medium, Gibco BRL) supplemented with 5% fetal bovine serum, 10 mM l−1 insulin and 1 mM l−1 hydrocortisone. Each of the Ads (dE1-RGD/GFP/shMot and dE1-RGD/GFP/scramble) at 1 × 1010 VP were added into the plates containing keloid spheroid, and incubated at 37 °C in 5% CO2 incubator for 3 days. The transduced keloid spheroids were then fixed with 10% formalin, paraffin-embedded, and cut into 5-μm-thick sections.
Histology and immunohistochemistry
Representative sections were stained with hematoxylin and eosin (H & E) and Masson’s trichrome, and then examined by light microscopy. Keloid spheroid sections were incubated at 4 °C overnight with mouse anti-collagen type I (ab6308; Abcam, Ltd., Cambridge, UK), mouse anti-collagen type III (C7805; Sigma, St. Louis, MO), mouse anti-elastin (E4013; Sigma), mouse anti-fibronectin (sc-52331; Santa Cruz Biotechnology), rabbit anti-TGF-β1 (ab9758; Abcam, Cambridge, UK), mouse anti-EGFR (Ab-1; Oncogene Research Products, Calbiochem), rabbit anti-Erk 1/2 (#4370 S; Cell Signaling Technology, Beverly, MA), and rabbit anti-Smad 2/3 complex (#8685 S; Cell Signaling Technology) mouse anti-PCNA (DAKO), goat anti-Cytochrome c (SC-8385; Santa Cruz Biotechnology) primary antibody, and then incubated at room temperature for 20 min with the Dako Envision™ Kit (DAKO, Glostrup, Denmark) as secondary antibody. Diaminobenzidine/hydrogen peroxidase (DAKO, Carpinteria, CA) was used as the chromogen substrate. All slides were counterstained with Meyer’s hematoxylin. The expression levels of TGF-β1, EGFR, Erk 1/2, Smad 2/3, type I and III collagen, elastin, and fibronectin were semi-quantitatively analyzed using MetaMorph® image analysis software (Universal Image Corp., Buckinghamshire, UK). Results are expressed as the mean optical density for six different digital images.
Western blot analysis
KFs were lysed in a solution containing 50 mM Tris-HCl (pH 7.6), 1% Nonidet P-40 (NP-40), 150 mM NaCl, 0.1 mM zinc acetate, and protease inhibitors. Protein concentration was determined by the Lowry method (Bio-Rad, Hercules, CA), and 30 μg of each sample was separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The proteins on the gel were electrotransferred to polyvinylidene fluoride membrane, incubated with the primary mouse anti-mortalin monoclonal antibody (C1-3) and rabbit anti-β-actin antibody (Sigma, St Louis, MO), and then secondarily incubated with the HRP (horseradish peroxidase)-conjugated secondary antibody (#7074 or 7076; Cell Signaling Technology). The expression patterns were revealed using the ECL detection kit (sc-2004; Santa Cruz Biotechnology), and the expression levels of mortalin was developed using enhanced chemiluminescence (Amersham Pharmacia Biotech, Uppsala, Sweden). Mortalin protein was semi-quantitatively analyzed using ImageJ software (National Institutes of Health, Bethesda, MD).
Immunofluorescence assay
Keloid tissue sections (n = 4) were deparaffinized, rehydrated, blocked with 5% goat serum, and incubated with mouse anti-mortalin monoclonal antibody (C1-3) or rabbit anti-p53 (sc-6243; Santa Cruz biotechnology) primary antibody overnight at 4 °C. Day after incubation, sections were washed with phosphate-buffered saline (PBS) and incubated with Alexa Flour 488-conjugated goat anti-mouse IgG (A11001; Invitrogen, Carlsbad, CA) or Alexa Flour 633-conjugated goat anti-rabbit IgG (A21070; Invitrogen) secondary antibody for 60 min at room temperature. Tissues were mounted on slides using Vectashield® mounting medium containing the nuclear stain DAPI (Vector Laboratories, Burlingame, CA), and viewed by confocal microscopy (LSM700, Olympus, Center Valley, PA).
Terminal Deoxynucleotidyl Transferase dUTP Nick End Labeling (TUNEL) assay
The apoptotic spheroid population was assessed by TUNEL assay as described previously (Gene Ther, 2008. 15(9): p. 635-51). The apoptotic cells were visually identified in five randomly selected fields and photographed at a magnification of x100 and x400. The expression level of apoptotic spheroid was semi-quantitatively analyzed using MetaMorph® image analysis software. Results are expressed as the mean optical density for five different digital images.
Statistics
Results are expressed as the mean ± standard error of the mean (SEM). Data were analyzed by a repeated-measures one-way ANOVA. Two sets of independent sample data were compared using a paired t-test; p-values < 0.05 was considered indicative of statistically significant differences.
References
Bran, G. M., Goessler, U. R., Hormann, K., Riedel, F. & Sadick, H. Keloids: current concepts of pathogenesis (review). International journal of molecular medicine 24, 283–293 (2009).
Tuan, T. L. & Nichter, L. S. The molecular basis of keloid and hypertrophic scar formation. Molecular Medicine Today 4, 19–24 (1998).
Shih, B., Garside, E., McGrouther, D. A. & Bayat, A. Molecular dissection of abnormal wound healing processes resulting in keloid disease. Wound Repair Regen 18, 139–153, https://doi.org/10.1111/j.1524-475X.2009.00553.x (2010).
Chipev, C. C. et al. Myofibroblast phenotype and apoptosis in keloid and palmar fibroblasts in vitro. Cell Death Differ 7, 166–176, https://doi.org/10.1038/sj.cdd.4400605 (2000).
Luo, S., Benathan, M., Raffoul, W., Panizzon, R. G. & Egloff, D. V. Abnormal balance between proliferation and apoptotic cell death in fibroblasts derived from keloid lesions. Plast Reconstr Surg 107, 87–96 (2001).
Ladin, D. A. et al. p53 and apoptosis alterations in keloids and keloid fibroblasts. Wound Repair Regen 6, 28–37 (1998).
Lu, F., Gao, J., Ogawa, R., Hyakusoku, H. & Ou, C. Biological differences between fibroblasts derived from peripheral and central areas of keloid tissues. Plast Reconstr Surg 120, 625–630, https://doi.org/10.1097/01.prs.0000270293.93612.7b (2007).
Saed, G. M. et al. Analysis of p53 gene mutations in keloids using polymerase chain reaction-based single-strand conformational polymorphism and DNA sequencing. Arch Dermatol 134, 963–967 (1998).
De Felice, B., Garbi, C., Santoriello, M., Santillo, A. & Wilson, R. R. Differential apoptosis markers in human keloids and hypertrophic scars fibroblasts. Mol Cell Biochem 327, 191–201, https://doi.org/10.1007/s11010-009-0057-x (2009).
Liu, W. et al. [Experimental study on p53 gene mutation in keloid fibroblasts]. Zhonghua Shao Shang Za Zhi 20, 85–87 (2004).
Heitzer, E. et al. Infrequent p53 gene mutation but UV gradient-like p53 protein positivity in keloids. Exp Dermatol 21, 277–280, https://doi.org/10.1111/j.1600-0625.2012.01450.x (2012).
De Felice, B. et al. Differential p63 and p53 expression in human keloid fibroblasts and hypertrophic scar fibroblasts. DNA Cell Biol 26, 541–547, https://doi.org/10.1089/dna.2007.0591 (2007).
Woods, D. B. & Vousden, K. H. Regulation of p53 function. Exp Cell Res 264, 56–66, https://doi.org/10.1006/excr.2000.5141 (2001).
Lindenboim, L., Borner, C. & Stein, R. Nuclear proteins acting on mitochondria. Biochim Biophys Acta 1813, 584–596, https://doi.org/10.1016/j.bbamcr.2010.11.016 (2011).
Kaul, S. C., Yaguchi, T., Taira, K., Reddel, R. R. & Wadhwa, R. Overexpressed mortalin (mot-2)/mthsp70/GRP75 and hTERT cooperate to extend the in vitro lifespan of human fibroblasts. Exp Cell Res 286, 96–101 (2003).
Wadhwa, R., Taira, K. & Kaul, S. C. An Hsp70 family chaperone, mortalin/mthsp70/PBP74/Grp75: what, when, and where? Cell Stress Chaperones 7, 309–316 (2002).
Wadhwa, R., Taira, K. & Kaul, S. C. Mortalin: a potential candidate for biotechnology and biomedicine. Histol Histopathol 17, 1173–1177 (2002).
Ran, Q. et al. Extramitochondrial localization of mortalin/mthsp70/PBP74/GRP75. Biochem Biophys Res Commun 275, 174–179, https://doi.org/10.1006/bbrc.2000.3237 (2000).
Kaul, S. C., Aida, S., Yaguchi, T., Kaur, K. & Wadhwa, R. Activation of wild type p53 function by its mortalin-binding, cytoplasmically localizing carboxyl terminus peptides. J Biol Chem 280, 39373-39379. https://doi.org/10.1074/jbc.M500022200 (2005).
Kaul, S. C., Taira, K., Pereira-Smith, O. M. & Wadhwa, R. Mort. alin: present and prospective. Exp Gerontol 37, 1157–1164 (2002).
Kaul, S. C., Deocaris, C. C. & Wadhwa, R. Three faces of mortalin: a housekeeper, guardian and killer. Exp Gerontol 42, 263–274, https://doi.org/10.1016/j.exger.2006.10.020 (2007).
Mihara, M. & Moll, U. M. Detection of mitochondrial localization of p53. Methods Mol Biol 234, 203–209, https://doi.org/10.1385/1-59259-408-5:203 (2003).
Saxena, N. et al. Molecular interactions of Bcl-2 and Bcl-xL with mortalin: identification and functional characterization. Biosci Rep 33, https://doi.org/10.1042/BSR20130034 (2013).
Deocaris, C. C., Kaul, S. C. & Wadhwa, R. On the brotherhood of the mitochondrial chaperones mortalin and heat shock protein 60. Cell Stress Chaperones 11, 116–128 (2006).
Lu, W. J. et al. Mortalin-p53 interaction in cancer cells is stress dependent and constitutes a selective target for cancer therapy. Cell Death Differ 18, 1046–1056, https://doi.org/10.1038/cdd.2010.177 (2011).
Lu, W. J. et al. Induction of mutant p53-dependent apoptosis in human hepatocellular carcinoma by targeting stress protein mortalin. Int J Cancer 129, 1806–1814, https://doi.org/10.1002/ijc.25857 (2011).
Wadhwa, R., Takano, S., Taira, K. & Kaul, S. C. Reduction in mortalin level by its antisense expression causes senescence-like growth arrest in human immortalized cells. J Gene Med 6, 439–444, https://doi.org/10.1002/jgm.530 (2004).
Ryu, J. et al. Identification and functional characterization of nuclear mortalin in human carcinogenesis. J Biol Chem 289, 24832–24844, https://doi.org/10.1074/jbc.M114.565929 (2014).
Wadhwa, R. & Kaul, S. C. In Mortalin Biology: Life, Stress and Death 3-20 (Springer, 2012).
Bellaye, P. S., Burgy, O., Causse, S., Garrido, C. & Bonniaud, P. Heat shock proteins in fibrosis and wound healing: good or evil? Pharmacology & therapeutics 143, 119–132, https://doi.org/10.1016/j.pharmthera.2014.02.009 (2014).
Cai, W. F. et al. Intracellular or extracellular heat shock protein 70 differentially regulates cardiac remodelling in pressure overload mice. Cardiovascular research 88, 140–149, https://doi.org/10.1093/cvr/cvq182 (2010).
Asea, A. et al. Novel signal transduction pathway utilized by extracellular HSP70: role of toll-like receptor (TLR) 2 and TLR4. The Journal of biological chemistry 277, 15028–15034, https://doi.org/10.1074/jbc.M200497200 (2002).
Lee, J. H. et al. Proteomic profiling reveals upregulated protein expression of hsp70 in keloids. BioMed research international 2013, 621538, https://doi.org/10.1155/2013/621538 (2013).
Chen, J. J. et al. Effect of heat shock protein 47 on collagen accumulation in keloid fibroblast cells. The British journal of dermatology 156, 1188–1195, https://doi.org/10.1111/j.1365-2133.2007.07898.x (2007).
Chen, J. J. et al. Effect of heat shock protein 47 on collagen synthesis of keloid in vivo. ANZ journal of surgery 81, 425–430 (2011).
Vousden, K. H. & Prives, C. Blinded by the Light: The Growing Complexity of p53. Cell 137, 413–431, https://doi.org/10.1016/j.cell.2009.04.037 (2009).
Laptenko, O. & Prives, C. Transcriptional regulation by p53: one protein, many possibilities. Cell death and differentiation 13, 951–961, https://doi.org/10.1038/sj.cdd.4401916 (2006).
Kaul, S. C. et al. Malignant transformation of NIH3T3 cells by overexpression of mot-2 protein. Oncogene 17, 907–911, https://doi.org/10.1038/sj.onc.1202017 (1998).
Xu, J., **ao, H. H. & Sartorelli, A. C. Attenuation of the induced differentiation of HL-60 leukemia cells by mitochondrial chaperone HSP70. Oncology research 11, 429–435 (1999).
Ahi, Y. S., Bangari, D. S. & Mittal, S. K. Adenoviral vector immunity: its implications and circumvention strategies. Current gene therapy 11, 307–320 (2011).
Lee, W., Kim, Y., Choi, I., Rah, D. & Yun, C. O. Adenovirus‐relaxin gene therapy for keloids: implication for reversing pathological fibrosis. British Journal of Dermatology 165, 673–677 (2011).
Lee, W. J. et al. Relaxin-expressing adenovirus decreases collagen synthesis and up-regulates matrix metalloproteinase expression in keloid fibroblasts: in vitro experiments. Plastic and reconstructive surgery 130, 407e–417e (2012).
Wu, H., Yoon, A. R., Li, F., Yun, C. O. & Mahato, R. I. RGD peptide-modified adenovirus expressing hepatocyte growth factor and X-linked inhibitor of apoptosis improves islet transplantation. J Gene Med 13, 658–669, https://doi.org/10.1002/jgm.1626 (2011).
Yoo, J. Y. et al. Tumor suppression by apoptotic and anti-angiogenic effects of mortalin-targeting adeno-oncolytic virus. J Gene Med 12, 586–595, https://doi.org/10.1002/jgm.1471 (2010).
Yoo, J. Y. et al. Short hairpin RNA-expressing oncolytic adenovirus-mediated inhibition of IL-8: effects on antiangiogenesis and tumor growth inhibition. Gene Ther 15, 635–651, https://doi.org/10.1038/gt.2008.3 (2008).
Yoo, J. Y. et al. VEGF-specific short hairpin RNA-expressing oncolytic adenovirus elicits potent inhibition of angiogenesis and tumor growth. Mol Ther 15, 295–302, https://doi.org/10.1038/sj.mt.6300023 (2007).
Acknowledgements
This work was supported by grants from the Korea Science and Engineering Foundation (2015R1A2A1A13027811, 2016M3A9B5942352 and 2013M3A9D3045879, Dr. C-O. Yun), the National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST) (No. 2014051295, WJ Lee).
Author information
Authors and Affiliations
Contributions
W.J. Lee collected, designed, analyzed data, and wrote the manuscript; H.M. Ahn, Y.J. Na, and J.W. Hong performed experiments and analyzed data; R. Wadhwa analyzed and discussed data; C.O. Yun supervised the whole process of the study and wrote the manuscript. All authors contributed to this article.
Corresponding author
Ethics declarations
Competing Interests
The authors declare that they have no competing interests.
Additional information
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Electronic supplementary material
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Lee, W.J., Ahn, H.M., Na, Y. et al. Mortalin deficiency suppresses fibrosis and induces apoptosis in keloid spheroids. Sci Rep 7, 12957 (2017). https://doi.org/10.1038/s41598-017-13485-y
Received:
Accepted:
Published:
DOI: https://doi.org/10.1038/s41598-017-13485-y
- Springer Nature Limited
This article is cited by
-
Targeting the Akt/PI3K/mTOR signaling pathway for complete eradication of keloid disease by sunitinib
Apoptosis (2022)
-
Mortaparib, a novel dual inhibitor of mortalin and PARP1, is a potential drug candidate for ovarian and cervical cancers
Journal of Experimental & Clinical Cancer Research (2019)