Cultured circular smooth muscle from the rabbit colon

• Published in: In vitro cellular & developmental biology Vol. 24; no. 8; p. 787
• Main Authors: Kao, H W, Finn, S E, Gown, A M, Lechago, J, Lachant, N, Snape, Jr, W J
• Format: Journal Article
• Language: English
• Published: United States 01.08.1988
• Subjects: Animals; Cell Division; Cells, Cultured; Colon - cytology; Fluorescent Antibody Technique; Microscopy, Electron; Muscle, Smooth - cytology; Rabbits
• ISSN: 0883-8364
• DOI: 10.1007/BF02623649

Although cultured vascular smooth muscle cells have been extensively characterized and investigated, there are very few studies of cultured intestinal smooth muscle cells. The aim of this study was to culture colonic smooth muscle (CSM) cells from the rabbit colon. Freshly isolated CSM cells from the circular muscle layer of the distal colon were prepared by collagenase digestion. In primary culture, CSM cells attached to the culture vessels by 48 to 72 h, proliferated by 3 to 7 d, and reached confluency by 14 to 17 d with a "hill-and-valley" pattern. Spontaneous contractions were not observed at any time at 21 degrees or 37 degrees C. Confluent primary cultures were greater than 95% CSM cells, as identified by intensely positive immunofluorescent staining to smooth muscle actin-specific CGA7 and muscle-specific HHF-35 monoclonal antibodies. Transmission electron microscopy of freshly isolated and proliferating CSM cells revealed ultrastructural features consistent with smooth muscle cells. We successfully cultured CSM cells of the rabbit from freshly isolated cells and validated these CSM cells by electron microscopy and immunocytochemical staining. These highly pure primary cultures may be used to investigate numerous aspects of CSM cell metabolism and physiology.