Outcomes obtained in patients with two-tendon rotator cuff tear submitted to repair reinforced with porcine small intestinal submucosa (SIS) have not been as encouraging as those observed in animal models. We verify the capacity of SIS to be used as a physical support for a culture of cuff cells. During arthroscopic repairs of large rotator cuff tears, we removed a fragment of supraspinatus tendon. Samples were treated for obtaining a cuff cell culture. Daily microscopic analysis, to observe adhesion to substrate, replication and cell shape was performed. A confluent monolayer was obtained in 1 week. Cells at the second passage were collected and seeded onto scaffold and cultured for 7-30 days. A morphological and immunohistochemical evaluation was performed. After 1 week, a monolayer of tendinous-like cells lay along the surface of the SIS. Within two weeks, a multicellular layer was observable in many foci of the scaffold. After a month, the cells completely invaded the numerous splits of the SIS and were positive to monoclonal anti-type I collagen antibody. Our experimental study has proved that a cuff cell culture can be performed using SIS as substrate. The culture covers the SIS surface, therefore it may reduce immune or non-specific inflammatory reactions.

Culture of rotator cuff cells on orthobiologic support (porcine small intestinal submucosa) / Gumina, Stefano; A., Patti; A., Vulcano; DELLA ROCCA, Carlo; Postacchini, Franco. - STAMPA. - (2005), pp. 77-77. (Intervento presentato al convegno 19th SECEC congress tenutosi a Rome nel 21-24 September, 2005).

Culture of rotator cuff cells on orthobiologic support (porcine small intestinal submucosa)

GUMINA, STEFANO;DELLA ROCCA, Carlo;POSTACCHINI, Franco
2005

Abstract

Outcomes obtained in patients with two-tendon rotator cuff tear submitted to repair reinforced with porcine small intestinal submucosa (SIS) have not been as encouraging as those observed in animal models. We verify the capacity of SIS to be used as a physical support for a culture of cuff cells. During arthroscopic repairs of large rotator cuff tears, we removed a fragment of supraspinatus tendon. Samples were treated for obtaining a cuff cell culture. Daily microscopic analysis, to observe adhesion to substrate, replication and cell shape was performed. A confluent monolayer was obtained in 1 week. Cells at the second passage were collected and seeded onto scaffold and cultured for 7-30 days. A morphological and immunohistochemical evaluation was performed. After 1 week, a monolayer of tendinous-like cells lay along the surface of the SIS. Within two weeks, a multicellular layer was observable in many foci of the scaffold. After a month, the cells completely invaded the numerous splits of the SIS and were positive to monoclonal anti-type I collagen antibody. Our experimental study has proved that a cuff cell culture can be performed using SIS as substrate. The culture covers the SIS surface, therefore it may reduce immune or non-specific inflammatory reactions.
2005
19th SECEC congress
rotator cuff healing
04 Pubblicazione in atti di convegno::04b Atto di convegno in volume
Culture of rotator cuff cells on orthobiologic support (porcine small intestinal submucosa) / Gumina, Stefano; A., Patti; A., Vulcano; DELLA ROCCA, Carlo; Postacchini, Franco. - STAMPA. - (2005), pp. 77-77. (Intervento presentato al convegno 19th SECEC congress tenutosi a Rome nel 21-24 September, 2005).
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/489371
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