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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

In vivo evidence of angiogenesis inhibition by beta(2)-glycoprotein I subfractions in the chorioallantoic membrane of chicken embryos

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Author(s):
Baldavira, C. M. [1] ; Gomes, L. F. [2] ; De La Cruz, L. T. [3] ; Maria, D. A. [4] ; Capelozzi, V. L. [1]
Total Authors: 5
Affiliation:
[1] Univ Sao Paulo, Fac Med, Dept Patol, Sao Paulo, SP - Brazil
[2] Univ Sao Paulo, Fac Ciencias Farmaceut, Dept Anal Clin & Toxicol, Sao Paulo, SP - Brazil
[3] Univ Sao Paulo, Inst Oceanog, Lab Sistemas Plancton, Sao Paulo, SP - Brazil
[4] Inst Butantan, Lab Biol Mol, Sao Paulo, SP - Brazil
Total Affiliations: 4
Document type: Journal article
Source: Brazilian Journal of Medical and Biological Research; v. 54, n. 3 2021.
Web of Science Citations: 0
Abstract

The vascular network expansion and functioning are important factors affecting normal intra-uterine fetal development. This study addressed the previously reported antiangiogenic potential of beta-2-glycoprotein I (beta(2)GPI) in vivo in the chick embryo model of angiogenesis. The effects of two naturally occurring beta(2)GPI forms on the development of the chorioallantoic membrane (CAM) vessels and the chicken embryo were investigated. beta(2)GPI monomers and dimers were obtained by fractioned purification and characterized using SDS-PAGE, immunoblot, and ELISA. The egg exposure was performed by injection of small volumes of 2.5 mu g/mL solutions of the beta(2)GPI subfractions. Angiogenesis was evaluated through quantitative measurements of vascular architecture parameters in the captured CAM images, using computational analysis of texture contrasts and computer vision techniques. Quantitative information was assigned to the CAM vasculature modifications. In vivo, the beta(2)GPI dimer completely halted the formation of CAM vessels and led to embryo death after 48 h of exposure. The beta(2)GPI monomer allowed the embryo to develop up to the 10th day, despite early changes of CAM vessels. The impaired normal vessel growth proceeded as a self-limited effect. The beta(2)GPI monomer-exposed eggs showed reduced vascularization on the 6th day of incubation, but embryos were viable on the 10th day of incubation, with ingurgitated CAM vessels implying sequelae of the angiogenesis inhibition. Both subfractions impaired CAM vasculature development. The beta(2)GPI dimer proved to be largely more harmful than the beta(2)GPI monomer. beta(2)GPI modification by cleavage or dimerization may play a role in angiogenesis control in vivo. (AU)

FAPESP's process: 18/20403-6 - Biomolecular markers of proliferation and remodeling in acute and chronic respiratory diseases: promising therapeutic targets
Grantee:Vera Luiza Capelozzi
Support Opportunities: Research Projects - Thematic Grants