Stress fibers in cells in situ: immunofluorescence visualization with antiactin, antimyosin, and anti-alpha-actinin
نویسندگان
چکیده
Stress fiber-like patterns are visualized by indirect immunofluorescence in scleroblasts (fibroblasts) in situ on the scale of the common goldfish, Carassius auratus, using an affinity-purified antiactin, antimyosin, and anti-alpha-actinin. These fibers demonstrate the classical convergent and parallel patterns exhibited by stress fibers in tissue culture cells. Because the dimensions, the composition, and the pattern of distribution of these cytoplasmic fibers correspond well with those of stress fibers in cultured cells, we will call these fibers stress fibers also. The staining patterns with anti-alpha-actinin and antimyosin along the stress fibers often reveal a periodicity of 1-2 microM, identical to that found in cells in vitro. The majority of scleroblasts do not exhibit stress fiber staining and they are specifically located in the central regions of the scale. Stress fibers are present in scleroblasts residing on or near the edges or radical ridges of the scale. They are consistently orientated perpendicular to these structures; however, unlike microtubules, stress fibers show no co-alignment with collagen fibers of the scale. The finding that stress fibers are located in regions of the scale more subject to shearing forces may indicate their role in increased cellular adhesion to the substratum.
منابع مشابه
Improved fixation for immunofluorescence microscopy using light- activated 1,3,5-triazido-2,4,6-trinitrobenzene (TTB)
A new fixation method has been developed for immunofluorescent microscopy using the photosensitive compound 1,3,5-triazido-2,4,6-trinitrobenzene (TTB). Our results show that TTB-fixed cells are well preserved morphologically and that the cellular antigens are better preserved than conventionally fixed cells. By altering one condition at a time in the TTB fixation procedure and analyzing resulti...
متن کاملDifferences in the stress fibers between fibroblasts and epithelial cells
In the stress fibers of two types of nonmuscle cells, epithelia (PtK2, bovine lens) and fibroblasts (Gerbil fibroma, WI-38, primary human) the spacing between sites of alpha-actinin localization differs by a factor of about 1.6 as determined by indirect immunofluorescence and ultrastructural localization with peroxidase-labeled antibody. Both methods reveal striations along the stress fibers wi...
متن کاملUltrastructural localization of alpha-actinin and filamin in cultured cells with the immunogold staining (IGS) method
Monospecific antibodies to chicken gizzard actin, alpha-actinin, and filamin have been used to localize these proteins at the ultrastructural level: secondary cultures of 14-d-old chicken embryo lung epithelial cells and chicken heart fibroblasts were briefly lysed with either a 0.5% Triton X-100/0.25% glutaraldehyde mixture, or 0.1% Triton X-100, fixed with 0.5% glutaraldehyde, and further per...
متن کاملNerve fibers in culture and their interactions with non-neural cells visualized by immunofluorescence
Cultures of embryonic mouse spinal cord explants, alone or in combination with rat myotubes, were stained by indirect immunofluorescence using antibodies against three structural proteins to: (a) reveal the distribution of these proteins among different cell types, and (b) test the usefulness of antibody staining to reveal the gross morphology of the neurite network in complex cultures. Affinit...
متن کاملCultured megakaryocytes: changes in the cytoskeleton after ADP-induced spreading
Megakaryocytes from guinea pig bone marrow were isolated and maintained in liquid culture and were treated with ADP, thrombin, arachidonic acid, or collagen. Megakaryocytes spread with an active ruffled membrane in response to ADP (1-100 microM), thrombin (1.0 U/ml), and arachidonic acid (50 microM) but responded to collagen surfaces only if fibronectin was added to the cultures. Spreading coul...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Journal of Cell Biology
دوره 93 شماره
صفحات -
تاریخ انتشار 1982