4.3 Article

Molecular and Cellular Characterization of Space Flight Effects on Microvascular Endothelial Cell Function - PreparatoryWork for the SFEF Project

期刊

MICROGRAVITY SCIENCE AND TECHNOLOGY
卷 26, 期 6, 页码 351-363

出版社

SPRINGER
DOI: 10.1007/s12217-014-9399-4

关键词

Microvascular endothelial cells; HMEC-1; Microgravity; International Space Station; Cosmic radiation; Senescence; Prenosological medicine; Epigenetics; Transcriptomics; Immunofluorescence

资金

  1. European Space Agency
  2. Agenzia Spaziale Italiana [5681]
  3. Regione Toscana [POR FSE 2007-2013-FORTEC]
  4. Kayser Italia S.r.l.

向作者/读者索取更多资源

Exposure to microgravity during space flight (SF) of variable length induces suffering of the endothelium (the cells lining all blood vessels), mostly responsible for health problems found in astronauts and animals returning from space. Of interest to pre-nosological medicine, the effects of microgravity on astronauts are strikingly similar to the consequences of sedentary life, senescence and degenerative diseases on Earth, although SF effects are accelerated and reversible. Thus, microgravity is a significant novel model for better understanding of common pathologies. A comprehensive cell and molecular biology study is needed in order to explain pathophysiological findings after SFs. This project will study the effects of microgravity and cosmic radiation on endothelial cells (ECs) cultured on the International Space Station through analysis of 1) cell transcriptome, 2) DNA methylome, 3) DNA damage and cell senescence, 4) variations in cell cycle and cell morphology. This project has been selected by the European Space Agency and the Italian Space Agency and is presently in preparation. The ground study presented here was performed to determine the biological and engineering requirements that will allow us to retrieve suitable samples after culturing, fixing and storing ECs in space. We expect to identify molecular pathways activated by space microgravity in microvascular ECs, which may shed light on pathogenic molecular mechanisms responsible for endothelial suffering shared by astronauts and individuals affected with aging, degenerative and sedentary life-associated pathologies on Earth.

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