Rapid Homeostatic Turnover of Embryonic ECM during Tissue Morphogenesis
Authors: Matsubayashi, Y., Sánchez-Sánchez, B.J., Marcotti, S., Serna-Morales, E., Dragu, A., Díaz-de-la-Loza, M.D.C., Vizcay-Barrena, G., Fleck, R.A. and Stramer, B.M.
Journal: Developmental Cell
Volume: 54
Issue: 1
Pages: 33-42.e9
eISSN: 1878-1551
ISSN: 1534-5807
DOI: 10.1016/j.devcel.2020.06.005
Abstract:The extracellular matrix (ECM) is hypothesized to form a long-lived cellular scaffold. Using modeling and in vivo pulse-chase experiments, Matsubayashi, Sánchez-Sánchez et al. show that the embryonic fruit fly ECM has a surprisingly short half-life. This labile ECM network is likely necessary to maintain plasticity for growth and morphogenesis.
Source: Scopus
Rapid Homeostatic Turnover of Embryonic ECM during Tissue Morphogenesis.
Authors: Matsubayashi, Y., Sánchez-Sánchez, B.J., Marcotti, S., Serna-Morales, E., Dragu, A., Díaz-de-la-Loza, M.-D.-C., Vizcay-Barrena, G., Fleck, R.A. and Stramer, B.M.
Journal: Dev Cell
Volume: 54
Issue: 1
Pages: 33-42.e9
eISSN: 1878-1551
DOI: 10.1016/j.devcel.2020.06.005
Abstract:The extracellular matrix (ECM) is a polymer network hypothesized to form a stable cellular scaffold. While the ECM can undergo acute remodeling during embryogenesis, it is experimentally difficult to determine whether basal turnover is also important. Most studies of homeostatic turnover assume an initial steady-state balance of production and degradation and measure half-life by quantifying the rate of decay after experimental intervention (e.g., pulse labeling). Here, we present an intervention-free approach to mathematically model basal ECM turnover during embryogenesis by exploiting our ability to live image de novo ECM development in Drosophila to quantify production from initiation to homeostasis. This reveals rapid turnover (half-life ∼7-10 h), which we confirmed by in vivo pulse-chase experiments. Moreover, ECM turnover is partially dependent on proteolysis and network interactions, and slowing turnover affects tissue morphogenesis. These data demonstrate that embryonic ECM undergoes constant replacement, which is likely necessary to maintain network plasticity to accommodate growth and morphogenesis.
Source: PubMed
Rapid Homeostatic Turnover of Embryonic ECM during Tissue Morphogenesis
Authors: Matsubayashi, Y., Sanchez-Sanchez, B.J., Marcotti, S., Serna-Morales, E., Dragu, A., Diaz-de-la-Loza, M.-D.-C., Vizcay-Barrena, G., Fleck, R.A. and Stramer, B.M.
Journal: DEVELOPMENTAL CELL
Volume: 54
Issue: 1
Pages: 33-+
eISSN: 1878-1551
ISSN: 1534-5807
DOI: 10.1016/j.devcel.2020.06.005
Source: Web of Science (Lite)
Rapid Homeostatic Turnover of Embryonic ECM during Tissue Morphogenesis.
Authors: Matsubayashi, Y., Sánchez-Sánchez, B.J., Marcotti, S., Serna-Morales, E., Dragu, A., Díaz-de-la-Loza, M.-D.-C., Vizcay-Barrena, G., Fleck, R.A. and Stramer, B.M.
Journal: Developmental cell
Volume: 54
Issue: 1
Pages: 33-42.e9
eISSN: 1878-1551
ISSN: 1534-5807
DOI: 10.1016/j.devcel.2020.06.005
Abstract:The extracellular matrix (ECM) is a polymer network hypothesized to form a stable cellular scaffold. While the ECM can undergo acute remodeling during embryogenesis, it is experimentally difficult to determine whether basal turnover is also important. Most studies of homeostatic turnover assume an initial steady-state balance of production and degradation and measure half-life by quantifying the rate of decay after experimental intervention (e.g., pulse labeling). Here, we present an intervention-free approach to mathematically model basal ECM turnover during embryogenesis by exploiting our ability to live image de novo ECM development in Drosophila to quantify production from initiation to homeostasis. This reveals rapid turnover (half-life ∼7-10 h), which we confirmed by in vivo pulse-chase experiments. Moreover, ECM turnover is partially dependent on proteolysis and network interactions, and slowing turnover affects tissue morphogenesis. These data demonstrate that embryonic ECM undergoes constant replacement, which is likely necessary to maintain network plasticity to accommodate growth and morphogenesis.
Source: Europe PubMed Central