Dataset Information

Schwann Cells Migration on Patterned Polydimethylsiloxane Microgrooved Surface.

ABSTRACT: Schwann cells (SCs) aid in nerve repair in the peripheral nervous system, and their ability to migrate into the injury site is critical for nerve regeneration after injury. The majority of studies on SC behavior have focused on SC alignment through contact guidance, rather than migration. The few studies on SC migration primarily investigated the migration of individual cells over several hours with time-lapse microscopy. However, during neural tissue repair, SCs do not migrate as single cells but as a population of cells over physiologically relevant time and length scales. Thus from a practical perspective, there is a need to understand the migration of large populations of SC and the collective guidance cues from the surrounding environment in designing optimal transplantable scaffolds. This study investigates a large population of migrating SCs over a period of 2 weeks on patterned polydimethylsiloxane (PDMS) microgrooved channels of different sizes. Two methods were used to quantify the migration velocity of a large cell population that minimized the confounding effect due to cell proliferation: one based on a leading edge velocity and a second based on a binary velocity. Both approaches showed that the SC population migrated the fastest on the smallest sized microgrooved channels. The insights provided in this study could inform on future designs of transplantable scaffolds for peripheral nerve regeneration.

SUBMITTER: Liu C

PROVIDER: S-EPMC4943468 | biostudies-literature | 2016 Jul

REPOSITORIES: biostudies-literature

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Schwann Cells Migration on Patterned Polydimethylsiloxane Microgrooved Surface.

Liu Chun C Kray Jeremy J Toomajian Victoria V Chan Christina C

Tissue engineering. Part C, Methods 20160622 7

Schwann cells (SCs) aid in nerve repair in the peripheral nervous system, and their ability to migrate into the injury site is critical for nerve regeneration after injury. The majority of studies on SC behavior have focused on SC alignment through contact guidance, rather than migration. The few studies on SC migration primarily investigated the migration of individual cells over several hours with time-lapse microscopy. However, during neural tissue repair, SCs do not migrate as single cells b ...[more]

PMID: 27216726

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Project description:Mesenchymal stem cells' (MSCs) fate is largely determined by the various topographical features and a range of extracellular matrix (ECM) components present in their niches. Apart from maintaining structural stability, they regulate cell morphology, division, proliferation, migration and differentiation among others. Traditional MSC cultures, which are mainly based on two-dimensional smooth surfaces of culture dishes and plates, do not provide topographical cues similar to in vivo three-dimensional niches, impacting various cellular processes. Therefore, we culture the mouse bone marrow-derived MSCs on microgrooved bearing surface, partially mimicking in vivo reticulated niche, to study its effect on morphology, pluripotency factor-associated stemness, cell division and rate of proliferation. Following culture, morphological features, and MSC-specific marker gene expression, such as CD29, CD44, Sca-1 along with HSC (Haematopoietic stem cell)-specific markers like CD34, CD45, CD11b were evaluated by microscopy and immunophenotyping, respectively. HSC is another type of bone marrow stem cell population, which concertedly interacts with MSC during various functions, including haematopoiesis. In addition, mesenchymal stem cells were further analyzed for gene expression of pluripotency-associated transcription factors such as Oct3/4, Sox-2, Nanog and Myc, as well as differentiated into adipocytes, osteocytes and chondrocytes. Our results show that microgrooved surface-cultured mesenchymal stem cells (MMSCs) expressed higher levels of expected cell surface and pluripotency-associated markers and proliferated more rapidly (2-3×fold) with higher percentage of cells in S/G2-M-phase, consequently giving rise to higher cell yield compared to standard culture flask-grown cells (MSCs), taken as control. Furthermore, both MSCs and MMSCs showed considerable accumulation of intracellular lipid-droplets, higher alkaline phosphatase activity and secretion of extracellular matrix that are characteristics of adipogenesis, osteogenesis and chondrogenesis, respectively.

Dataset Information

Schwann Cells Migration on Patterned Polydimethylsiloxane Microgrooved Surface.

Publications

Schwann Cells Migration on Patterned Polydimethylsiloxane Microgrooved Surface.

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