Lasek Raymond J.

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Lasek
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Raymond J.
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  • Book
    A guide to laboratory use of the squid Loligo pealei
    (Marine Biological Laboratory, 1974) Arnold, John M. ; Summers, William C. ; Gilbert, Daniel L. ; Manalis, Richard S. ; Daw, Nigel W. ; Lasek, Raymond J.
    From the Preface: Unfortunately, a guide like this one does not happen simply. It is the product of polite requests (at first polite, anyway) from colleagues, of mutual nagging, and of wives with persistant memories. What we are attempting to achieve with this contribution is a consolidation of many years of personal experience with squid into a source of practical information hopefully useful to the increasing number of people working with the squid. One does not undertake the task of preparing such a guide for a limited audience with unreserved enthusiasm. It always seems the same amount of work could produce something for a larger audience and therefore, hopefully, of greater significance. On the other hand when the hours and days spent on developing handling procedures, techniques, and "tricks of the squid trade" are considered it seems untenable not to pass this otherwise unpublishable data on in hope of saving others like pain and time. Therefore, what we have attempted to do is informally put together information that should prove useful to people interested in all aspects of squid biology. In this way we hope to make the laboratory utilization of the squid more efficient not only from the standpoint of the investigator and the collector but also for the future of the species Loligo pealei.
  • Article
    Axonal maintenance, glia, exosomes, and heat shock proteins
    (F1000 Research, 2016-02-22) Tytell, Michael ; Lasek, Raymond J. ; Gainer, Harold
    Of all cellular specializations, the axon is especially distinctive because it is a narrow cylinder of specialized cytoplasm called axoplasm with a length that may be orders of magnitude greater than the diameter of the cell body from which it originates. Thus, the volume of axoplasm can be much greater than the cytoplasm in the cell body. This fact raises a logistical problem with regard to axonal maintenance. Many of the components of axoplasm, such as soluble proteins and cytoskeleton, are slowly transported, taking weeks to months to travel the length of axons longer than a few millimeters after being synthesized in the cell body. Furthermore, this slow rate of supply suggests that the axon itself might not have the capacity to respond fast enough to compensate for damage to transported macromolecules. Such damage is likely in view of the mechanical fragility of an axon, especially those innervating the limbs, as rapid limb motion with high impact, like running, subjects the axons in the limbs to considerable mechanical force. Some researchers have suggested that local, intra-axonal protein synthesis is the answer to this problem. However, the translational state of axonal RNAs remains controversial. We suggest that glial cells, which envelop all axons, whether myelinated or not, are the local sources of replacement and repair macromolecules for long axons. The plausibility of this hypothesis is reinforced by reviewing several decades of work on glia-axon macromolecular transfer, together with recent investigations of exosomes and other extracellular vesicles, as vehicles for the transmission of membrane and cytoplasmic components from one cell to another.