Both protein activation and gene expression are involved in early vascular tube formation in vitro - PubMed (original) (raw)
Affiliations
- PMID: 12231549
Both protein activation and gene expression are involved in early vascular tube formation in vitro
Andrew D Grove et al. Clin Cancer Res. 2002 Sep.
Abstract
Purpose: Gene expression and protein translation regulate and direct endothelial cell proliferation and differentiation. We initiated an unbiased global search for transcriptional changes occurring during endothelial cell vascular differentiation in vitro, focusing on genes not previously implicated in vascularization and angiogenesis.
Experimental design: cDNA and protein from human umbilical vein endothelial cells forming vascular tubes on the basement membrane surrogate, Matrigel, were collected and subjected to a global unbiased search for alterations in expression of genes not previously linked to angiogenesis.
Results: Transcriptional inhibitors blocked vascular tube formation only when present within the first hour of incubation (P < 0.05). cDNA array analysis yielded 31 differentially regulated transcripts (of 5100 queried; false positive rate, 0.4%) from gene classes representing transcription, translational regulation, cell structure, and cell adhesion. mRNA levels of caldesmon, a cytoskeleton-associated protein not previously linked to angiogenesis, were markedly reduced during early tube formation. Caldesmon protein quantity was also markedly decreased as demonstrated by laser capture microdissection of tubule cells followed by immunoblotting. Strikingly, no significant changes in transcription of genes previously demonstrated to contribute to angiogenesis, invasion, or signal transduction contained on the array were observed. To investigate the possibility that posttranslational rather than transcriptional changes were involved in facilitating tube formation, we evaluated the activation status of two dominant signal pathways, RAS/mitogen-activated protein kinase and phosphatidylinositol 3-kinase/AKT. A net 3-fold reduction in phospho-AKT and a 4-fold reduction in phospho-extracellular signal-regulated kinase-1/2 occurred in a transcription-independent fashion.
Conclusions: These data suggest that both changes in gene expression and transcription-independent activation of signal transduction pathways may be involved in vascular tube formation. A combination of transcriptional and proteomic analysis has the potential to identify novel transcription-dependent and -independent molecular targets of angiogenesis.
Similar articles
- Visfatin activates eNOS via Akt and MAP kinases and improves endothelial cell function and angiogenesis in vitro and in vivo: translational implications for atherosclerosis.
Lovren F, Pan Y, Shukla PC, Quan A, Teoh H, Szmitko PE, Peterson MD, Gupta M, Al-Omran M, Verma S. Lovren F, et al. Am J Physiol Endocrinol Metab. 2009 Jun;296(6):E1440-9. doi: 10.1152/ajpendo.90780.2008. Epub 2009 Apr 7. Am J Physiol Endocrinol Metab. 2009. PMID: 19351806 - Visfatin induces human endothelial VEGF and MMP-2/9 production via MAPK and PI3K/Akt signalling pathways: novel insights into visfatin-induced angiogenesis.
Adya R, Tan BK, Punn A, Chen J, Randeva HS. Adya R, et al. Cardiovasc Res. 2008 May 1;78(2):356-65. doi: 10.1093/cvr/cvm111. Epub 2007 Dec 18. Cardiovasc Res. 2008. PMID: 18093986 - Rit, a non-lipid-modified Ras-related protein, transforms NIH3T3 cells without activating the ERK, JNK, p38 MAPK or PI3K/Akt pathways.
Rusyn EV, Reynolds ER, Shao H, Grana TM, Chan TO, Andres DA, Cox AD. Rusyn EV, et al. Oncogene. 2000 Sep 28;19(41):4685-94. doi: 10.1038/sj.onc.1203836. Oncogene. 2000. PMID: 11032018 - Role of Akt signaling in vascular homeostasis and angiogenesis.
Shiojima I, Walsh K. Shiojima I, et al. Circ Res. 2002 Jun 28;90(12):1243-50. doi: 10.1161/01.res.0000022200.71892.9f. Circ Res. 2002. PMID: 12089061 Review.
Cited by
- Beneficial effect of KYP-2047, a propyl-oligopeptidase inhibitor, on oral squamous cell carcinoma.
Scuderi SA, Casili G, Filippone A, Lanza M, Basilotta R, Giuffrida R, Munaò S, Colarossi L, Capra AP, Esposito E, Paterniti I. Scuderi SA, et al. Oncotarget. 2021 Dec 7;12(25):2459-2473. doi: 10.18632/oncotarget.28147. eCollection 2021 Dec 7. Oncotarget. 2021. PMID: 34917264 Free PMC article. - Cell force-mediated matrix reorganization underlies multicellular network assembly.
Davidson CD, Wang WY, Zaimi I, Jayco DKP, Baker BM. Davidson CD, et al. Sci Rep. 2019 Jan 9;9(1):12. doi: 10.1038/s41598-018-37044-1. Sci Rep. 2019. PMID: 30626885 Free PMC article. - Differential expression of splicing variants of the human caldesmon gene (CALD1) in glioma neovascularization versus normal brain microvasculature.
Zheng PP, Sieuwerts AM, Luider TM, van der Weiden M, Sillevis-Smitt PA, Kros JM. Zheng PP, et al. Am J Pathol. 2004 Jun;164(6):2217-28. doi: 10.1016/S0002-9440(10)63778-9. Am J Pathol. 2004. PMID: 15161654 Free PMC article. - Isolating bronchial epithelial cell preparations from gross lung specimens.
Kwon YJ, Lee SJ, Koh JS, Kim YJ, Park JH. Kwon YJ, et al. In Vitro Cell Dev Biol Anim. 2009 Oct;45(9):496-9. doi: 10.1007/s11626-009-9229-y. Epub 2009 Jul 17. In Vitro Cell Dev Biol Anim. 2009. PMID: 19609830 - Activated thrombin-activatable fibrinolysis inhibitor attenuates the angiogenic potential of endothelial cells: potential relevance to the breast tumour microenvironment.
Bazzi ZA, Balun J, Cavallo-Medved D, Porter LA, Boffa MB. Bazzi ZA, et al. Clin Exp Metastasis. 2017 Feb;34(2):155-169. doi: 10.1007/s10585-017-9837-y. Epub 2017 Jan 25. Clin Exp Metastasis. 2017. PMID: 28124276
MeSH terms
Substances
LinkOut - more resources
Miscellaneous