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      Cytokines and Angiogenesis in the Corpus Luteum

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          Abstract

          In adults, physiological angiogenesis is a rare event, with few exceptions as the vasculogenesis needed for tissue growth and function in female reproductive organs. Particularly in the corpus luteum (CL), regulation of angiogenic process seems to be tightly controlled by opposite actions resultant from the balance between pro- and antiangiogenic factors. It is the extremely rapid sequence of events that determines the dramatic changes on vascular and nonvascular structures, qualifying the CL as a great model for angiogenesis studies. Using the mare CL as a model, reports on locally produced cytokines, such as tumor necrosis factor α (TNF), interferon gamma (IFNG), or Fas ligand (FASL), pointed out their role on angiogenic activity modulation throughout the luteal phase. Thus, the main purpose of this review is to highlight the interaction between immune, endothelial, and luteal steroidogenic cells, regarding vascular dynamics/changes during establishment and regression of the equine CL.

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          Most cited references111

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          Angiogenesis in life, disease and medicine.

          The growth of blood vessels (a process known as angiogenesis) is essential for organ growth and repair. An imbalance in this process contributes to numerous malignant, inflammatory, ischaemic, infectious and immune disorders. Recently, the first anti-angiogenic agents have been approved for the treatment of cancer and blindness. Angiogenesis research will probably change the face of medicine in the next decades, with more than 500 million people worldwide predicted to benefit from pro- or anti-angiogenesis treatments.
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            Angiogenesis in cancer, vascular, rheumatoid and other disease.

            J Folkman (1995)
            Recent discoveries of endogenous negative regulators of angiogenesis, thrombospondin, angiostatin and glioma-derived angiogenesis inhibitory factor, all associated with neovascularized tumours, suggest a new paradigm of tumorigenesis. It is now helpful to think of the switch to the angiogenic phenotype as a net balance of positive and negative regulators of blood vessel growth. The extent to which the negative regulators are decreased during this switch may dictate whether a primary tumour grows rapidly or slowly and whether metastases grow at all.
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              The TNF receptor 1-associated protein TRADD signals cell death and NF-κB activation

                Author and article information

                Journal
                Mediators Inflamm
                Mediators Inflamm
                MI
                Mediators of Inflammation
                Hindawi Publishing Corporation
                0962-9351
                1466-1861
                2013
                11 June 2013
                : 2013
                : 420186
                Affiliations
                1CIISA, Department of Morphology and Function, Faculty of Veterinary Medicine, Technical University of Lisbon, Avenida da Universidade Técnica, 1300-477 Lisboa, Portugal
                2Institute of Animal Reproduction and Food Research of PAS, Ulica Bydgoska 7, 10-243 Olsztyn, Poland
                Author notes
                *António M. Galvão: agalvao@ 123456fmv.utl.pt

                Academic Editor: Jeffrey H. Ruth

                Article
                10.1155/2013/420186
                3693155
                23840095
                08c29e86-8dea-482e-8b55-adb82850aeb8
                Copyright © 2013 António M. Galvão et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 March 2013
                : 22 May 2013
                : 22 May 2013
                Categories
                Review Article

                Immunology
                Immunology

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