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Sarco(endo)plasmic Reticulum Ca²⁺ ATPases (SERCA1 and -2) in Human Extraocular Muscles

¹From the Departments of Clinical Science, Section of Ophthalmology, and ³Integrative Medical Biology, Section of Anatomy, University of Umeå, Umeå, Sweden; the ²Department of Biology, National University of Ireland, Maynooth, Ireland; and the ⁴Department of Musculoskeletal Research, University of Gävle, Gävle, Sweden.

PURPOSE. To investigate the composition of the fibers in human extraocular muscles (EOMs) with respect to the sarco(endo)plasmic reticulum Ca²⁺ATPases (SERCA)-1 and -2 and to investigate possible correlations between SERCA and myosin heavy chain (MyHC) composition.

METHODS. EOM samples were processed for immunocytochemistry with monoclonal antibodies specific against SERCA1 (fast isoform), SERCA2 (slow isoform), or different MyHCs. A total of 1571 fibers were analyzed. Microsomal EOM fractions were analyzed with SDS-PAGE and immunoblots.

RESULTS. The fast fibers, containing MyHCIIa, accounted for 79% of the fibers in the orbital layer (OL) and 74% in the global layer (GL). More than 99% of these fibers contained SERCA1, and 86% of them coexpressed SERCA1 and -2. Almost all slow fibers stained with SERCA2; 54% of those in the GL and all in the OL coexpressed SERCA1 and -2. Fifteen percent of the fibers in the GL and less than 1% in the OL were MyHCeom^pos/MyHCIIa^neg fibers. All these contained SERCA1 and in the OL also stained strongly with anti-SERCA2. Biochemically SERCA2 was more abundant than SERCA1.

CONCLUSIONS. The human EOMs had a very complex pattern of expression of the major protein regulating fiber relaxation rate. The coexistence of SERCA1 and -2, together with complex mixtures of MyHCs in most of the fibers provide the human EOMs with a unique molecular portfolio that allows a highly specific fine-tuning regimen of contraction and relaxation.

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