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Adam S Curtis

Publications and source records attributed to Adam S Curtis.

2 recordsLinked to original sources

Topographical guidance of intervertebral disc cell growth in vitro: towards the development of tissue repair strategies for the anulus fibrosus.

The anulus fibrosus (AF) of the intervertebral disc consists of concentric sheets of collagenous matrix that is synthesised during embryogenesis by aligned disc cells. This highly organised structure may be severely disrupted during disc degeneration and/or herniation. Cell scaffolds that incorporate topographical cues as contact guidance have been used successfully to promote the healing of injured tendons. Therefore, we have investigated the effects of topography on disc cell growth. We show that disc cells from the AF and nucleus pulposus (NP) behaved differently in monolayer culture on micro-grooved membranes of polycaprolactone (PCL). Both cell types aligned to and migrated along the membrane's micro-grooves and ridges, but AF cells were smaller (or less spread), more bipolar and better aligned to the micro-grooves than NP cells. In addition, AF cells were markedly more immunopositive for type I collagen, but less immunopositive for chondroitin-6-sulphated proteoglycans than NP cells. There was no evidence of extracellular matrix (ECM) deposition. Disc cells cultured on non-grooved PCL did not show any preferential alignment at sub-confluence and did not differ in their pattern of immunopositivity to those on grooved PCL. We conclude that substratum topography is effective in aligning disc cell growth and may be useful in tissue engineering for the AF. However, there is a need to optimise cell sources and/or environmental conditions (e.g. mechanical influences) to promote the synthesis of an aligned ECM.

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Chondrocyte aggregation on micrometric surface topography: a time-lapse study.

Cellular aggregation or mesenchymal "condensation" is a prerequisite in the process of chondrogenesis. It has been observed that during in vitro engineering of cartilage, chondrocytes form aggregates in the initial cell seeding process of polymer scaffolds. However, the exact mechanism behind this aggregation has yet to be elucidated, although cell collision has been implicated. As all polymers have a surface topography, we hypothesized that topography may play a role in chondrocyte aggregation. 1(st) and 2(nd) passage chondrocytes were seeded on micrometric topography ranging from 0.75 to 8 microm in depth and 5 to 12.5 microm in width. Both 1(st) and 2(nd) passage cells formed aggregates as cells collided, and larger aggregates formed as aggregates collided with each other on the grooves. Furthermore, aggregates migrated parallel to the direction of the groove long axis. F-actin organization was altered only in the cellular layer in direct contact with the surface; stress fibers oriented in the direction of the groove long axis. Chondrocytes maintained type II collagen expression on all groove depths. This study shows that micrometric grooves could be an effective means for studying chondrocyte aggregation, and could additionally be utilized in the regeneration of cartilage.

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