TY - JOUR
T1 - Mammalian myosin Iα is concentrated near the plasma membrane in nerve growth cones
AU - Lewis, A. K.
AU - Bridgman, P. C.
PY - 1996
Y1 - 1996
N2 - To determine if unconventional myosins play a role in nerve outgrowth, antibodies specific for rat brain derived mammalian myosin Iα (MMIα) were used to label cultured rat superior cervical ganglion nerve cells. Observations were made at both the light and electron microscopic level of resolution using preparative procedures designed to enhance the ability to precisely determine the relationship between antibody label and cellular structures in order to map the distribution and structural association of this myosin. Immunofluorescence showed that MMIα has a punctate distribution throughout the nerve cell body, neurites, and growth cones. In growth cones, MMIα staining is sometimes elevated in thin peripheral regions of high actin content at the leading edge. Immunoelectron microscopy using colloidal gold conjugated antibodies showed that in growth cones MMIα is absent from membranous organelles and is concentrated primarily in the cell cortex adjacent to the cell membrane. The cortical label is equally distributed between upper and lower membranes. The plasma membrane association of the MMIα label persists under conditions in which the actin cytoskeleton is perturbed or removed, suggesting a direct association between a fraction of MMIα and the plasma membrane. MMIα label is also associated with the non- cortical actin cytoskeleton. Partial disruption of the actin cytoskeleton using cytochalasin B causes redistribution of only a subset of MMIα label. These data suggest a complex relationship between MMIα, the actin cytoskeleton, and the plasma membrane in the growth cone. In contrast to its localization in the growth cone, in neuronal cell bodies MMIα is also associated with tubulovesicular structures. This suggests that at this location MMIα may either act as an organelle motor or is passively transported to the plasma membrane on vesicles.
AB - To determine if unconventional myosins play a role in nerve outgrowth, antibodies specific for rat brain derived mammalian myosin Iα (MMIα) were used to label cultured rat superior cervical ganglion nerve cells. Observations were made at both the light and electron microscopic level of resolution using preparative procedures designed to enhance the ability to precisely determine the relationship between antibody label and cellular structures in order to map the distribution and structural association of this myosin. Immunofluorescence showed that MMIα has a punctate distribution throughout the nerve cell body, neurites, and growth cones. In growth cones, MMIα staining is sometimes elevated in thin peripheral regions of high actin content at the leading edge. Immunoelectron microscopy using colloidal gold conjugated antibodies showed that in growth cones MMIα is absent from membranous organelles and is concentrated primarily in the cell cortex adjacent to the cell membrane. The cortical label is equally distributed between upper and lower membranes. The plasma membrane association of the MMIα label persists under conditions in which the actin cytoskeleton is perturbed or removed, suggesting a direct association between a fraction of MMIα and the plasma membrane. MMIα label is also associated with the non- cortical actin cytoskeleton. Partial disruption of the actin cytoskeleton using cytochalasin B causes redistribution of only a subset of MMIα label. These data suggest a complex relationship between MMIα, the actin cytoskeleton, and the plasma membrane in the growth cone. In contrast to its localization in the growth cone, in neuronal cell bodies MMIα is also associated with tubulovesicular structures. This suggests that at this location MMIα may either act as an organelle motor or is passively transported to the plasma membrane on vesicles.
KW - actin cytoskeleton
KW - cell motility
KW - immunoelectron microscopy
KW - immunofluorescence
KW - nerve outgrowth
UR - http://www.scopus.com/inward/record.url?scp=0030063433&partnerID=8YFLogxK
U2 - 10.1002/(SICI)1097-0169(1996)33:2<130::AID-CM5>3.0.CO;2-G
DO - 10.1002/(SICI)1097-0169(1996)33:2<130::AID-CM5>3.0.CO;2-G
M3 - Article
C2 - 8635202
AN - SCOPUS:0030063433
SN - 0886-1544
VL - 33
SP - 130
EP - 150
JO - Cell Motility and the Cytoskeleton
JF - Cell Motility and the Cytoskeleton
IS - 2
ER -