Behavior of sea urchin primary mesenchyme cells in artificial extracellular matrices |
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Authors: | Hideki Katow |
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Affiliation: | 1. Instituto de Nanociencia de Aragón (INA), Universidad de Zaragoza, C/Mariano Esquillor S/N, CP 50018, Zaragoza, Spain;2. Departamento de Física de la Materia Condensada, Facultad de Ciencias, C/ Pedro Cerbuna 12, 50009, Zaragoza, Spain;3. Laboratorio de Microscopias Avanzadas (LMA), Universidad de Zaragoza, C/Mariano Esquillor S/N, CP 50018, Zaragoza, Spain;4. Grupo de Nanomedicina-IDIVAL, Universidad de Cantabria, Herrera Oria s/n, CP 39011 Santander, Spain;1. Marine-Integrated Bionics Research Center, Pukyong National University, Busan 48513, South Korea;2. Interdisciplinary Program of Biomedical Mechanical & Electrical Engineering, Pukyong National University, Busan 48513, South Korea;3. Department of Biomedical Engineering and Center for Marine-Integrated Biomedical Technology (BK21 Plus), Pukyong National University, Busan 48513, South Korea |
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Abstract: | The primary mesenchyme cells (PMCs) were separated from the mesenchyme blastulae of Pseudocentrotus depressus using differential adhesiveness of these cells to plastic Petri dishes. These cells were incubated in various artificial extracellular matrices (ECMs) including horse serum plasma fibronectin, mouse EHS sarcoma laminin, mouse EHS sarcoma type IV collagen, and porcine skin dermatan sulfate. The cell behavior was monitored by a time-lapse videomicrograph and analysed with a microcomputer. The ultrastructure of the artificial ECM was examined by transmission electron microscopy (TEM), while the ultrastructure of the PMCs was examined by scanning electron microscopy (SEM). The PMCs did not migrate in type IV collagen gel, laminin or dermatan sulfate matrix either with or without collagen gel, whereas PMCs in the matrix which was composed of fibronectin and collagen gel migrated considerably. However, the most active and extensive PMC migration was seen in the matrix which contained dermatan sulfate in addition to fibronectin and collagen gel. This PMC migration involved an increase not only of migration speed but also of proportion of migration-promoted cells. These results support the hypothesis that the mechanism of PMC migration involves fibronectin, collagen and sulfated proteoglycans which contain dermatan sulfate. |
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