Biomedical subjects

W J Nelson

Publications and source records attributed to W J Nelson.

164 records · Page 10Linked to original sources

PubMedDate not supplied

Switching of subunit composition of muscle spectrin during myogenesis in vitro.

Spectrin comprises a family of polypeptides thought to be involved in mediating linkage of actin filaments to the plasma membrane in a wide variety of cell types (for reviews see refs 1-3). Spectrin is present as a tetramer composed of two non-identical subunits. Most cells express a common subunit with a molecular weight (Mr) of 240,000 (240 K; termed alpha-spectrin) in association with a polymorphic cell type-specific subunit: Mr 260 K in the intestinal terminal web (termed TW260), Mr 235 K in nervous tissue., liver, lymphocytes and fibroblasts (termed gamma-spectrin; also referred to as fodrin), and Mr 225/220 K in erythrocytes and adult cardiac and skeletal muscle (termed beta'- and beta-spectrin, respectively). We show here that primary chicken myoblasts express predominantly alpha gamma-spectrin, but on terminal differentiation in vitro the cells gradually switch to alpha beta-spectrin as a result of the onset of beta- and beta'-spectrin synthesis and by the subsequent differential stabilization of beta- and gamma-spectrin. This switching correlates with known changes in the biophysical properties and function of the developing muscle sarcolemma and cytoskeleton.

Animals↗

PubMedDate not supplied

Ankyrin binding to (Na+ + K+)ATPase and implications for the organization of membrane domains in polarized cells.

The interaction between membrane proteins and cytoplasmic structural proteins is thought to be one mechanism for maintaining the spatial order of proteins within functional domains on the plasma membrane. Such interactions have been characterized extensively in the human erythrocyte, where a dense, cytoplasmic matrix of proteins comprised mainly of spectrin and actin, is attached through a linker protein, ankyrin, to the anion transporter (Band 3). In several nonerythroid cell types, including neurons, exocrine cells and polarized epithelial cells homologues of ankyrin and spectrin (fodrin) are localized in specific membrane domains. Although these results suggest a functional linkage between ankyrin and fodrin and integral membrane proteins in the maintenance of membrane domains in nonerythroid cells, there has been little direct evidence of specific molecular interactions. Using a direct biological and chemical approach, we show here that ankyrin binds to the ubiquitous (Na+ + K+)ATPase, which has an asymmetrical distribution in polarized cells.

Animals↗