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1. |
THE DEVELOPMENT OF THE PERIPHERAL NERVE FIBRE |
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Biological Reviews,
Volume 35,
Issue 3,
1960,
Page 283-323
ARTHUR HUGHES,
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摘要:
SUMMARY1Theodore Schwann, in hisstudy on the cellular nature of animal tissues (1839), was the first to describe the development of peripheral nerves. He believed, however, that the nerve fibre was formed by fusion of a row of the cells, which have since borne his name, but which are now known to form only the sheath around the nerve fibre. The latter has a wholly separate origin.2The developing peripheral nerves of the tail of amphibian larvae have been studied by a series of authors, the first of which was Schwann himself. Hensen (1864) realized that in their earliest stage the nerves of the tail fin were devoid of nuclei. In the 1870?s, several authors described the apparent origin of nuclei there inde now. In 1886, however, Kölliker followed the multiplication by mitotic division of Schwann cells, to which, as he realized, belong all the nuclei associated with the developing nerve fibre.3Balfour (1876) maintained that the whole of the peripheral nervous system in elasmobranchs was formed from cells which migrated outwards from the spinal cord. Hensen (1876) believed that nerves were formed along the tracks of protoplasmic strands which ran the whole distance between centre and periphery, and which originated in the incomplete cleavage of cells in the ectodermal layer of the early embryo. These theories were opposed to the views of Bidder&Kupffer (1857), His (1879), and Ramon y Cajal(1890) all of whom described the development of peripheral nerves in terms of the outgrowth of fibres from cells within the spinal cord and ganglia.4Ramon y Cajal was the first to study the developing nervous system by metallic impregnation methods. He concluded that no fusion occurs at points where the processes of neighbouring cells come into contact. The concept of cellular individuality in the nervous system was the basis of the Neurone Theory of Waldeyer (1891).5The first attack on this theory came with the work of Apathy (1889) who claimed to be able to follow stainable fibrillar constituents of the nerve fibre, the ‘neurofibrilla’, through the junction of one nerve cell with the next. Apathy stated that they were the actual conducting elements of the nervous system. The study of neurofibrillae in the developing nervous system by various workers has led to no uniform concepts. Paton (1907) believed that they can enter the nerve cell from outside; Held (1909) claimed that a pre‐existing network served as a guide from the growing nerve fibre. In this respect Held's views approximate to those of Hensen.6Fresh support to the neurone theory was gained in the pioneer experiments of Ross Harrison (1907) in the cultivation of tissuesin vitro, in which he observed the outgrowth of living nerve fibres from amphibian neuroblasts into a medium of clotted fibrin. In the course of their growth such fibres received no support or any contribution from adjacent cells. Harrison described the detailed behaviour of the terminal growth cone, which had already been discovered by Ramon y Cajal.7Research on the outgrowth of nerve fibres has so far been largely confined to vertebrate embryos, though the ingrowth of axons from epidermal sensory cells in insects has been studied in recent years (Wigglesworth, 1953). In some invertebrates axons undergo an apparent secondary fusion to form giant fibres (Young, 1936), though the development of this condition has not yet been followed.8The outgrowth theory by itself leaves unexplained the forces which direct the nerve fibres during their growth. His (1887) believed that the fibre grows straight outwards until deflected by some structure lying across its path. Ramon y Cajal (1893) suggested that the outgrowing tips of nerve fibres were attracted towards their end organs by a chemotropic stimulus. Weiss, on the basis of experimental study on tissue cultures (1934), has elaborated a theory whereby a growing organ orientates intercellular material around itself, and so provides a pre‐formed pathway along which a growing fibre, with its accompanying Schwann cells, can reach its destination. Contact with surfaces is certainly an important factor in nerve outgrowth.9The mutual interactions of Schwann cells and nerve fibres in the living state have been extensively studied by Speidel(1932 onwards) in the tail fin of amphibian larvae. The progress of myelination is now being followed by means of the electron microscope (Geren, 1954).10Whatever the forces which direct growing nerve fibres, it is clear that there is no complete and detailed plan set before the unfolding peripheral nervous system from the outset, for some individual fibres choose random and aberrant paths. Ramon y Cajal (1908) was the first to point out the significance of these ‘fibres égarées’.11Although no direct experimental proof of chemotropic attraction of nerve fibres has been obtained, chemical forces are invoked in the adjustments which follow when a nerve has approached its end organ. On the motor side Weiss (1936) found that inAmblystomagrafted supernumerary limbs move in unison with an adjacent normal member. Corresponding muscles contract synchronously even though the anatomical pattern of their regenerated nerves may be aberrant. Weiss explained this ‘resonance effect’ by postulating that when a regenerating motor nerve reaches a muscle at random, a chemical stimulus is transmitted centripetally, which leads to rearrangement of central synaptic junctions. Similar readjustments are inferred in the experiments of Sperry (1951) in which areas of skin on the body surface of a tadpole are interchanged. A grafted patch continues to transmit to the centre information concerning location of the body surface which refers to its original site even though in its new position it is innervated by surroundin
ISSN:1464-7931
DOI:10.1111/j.1469-185X.1960.tb01326.x
出版商:Blackwell Publishing Ltd
年代:1960
数据来源: WILEY
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2. |
COMPENSATORY GROWTH AFTER UNDERNUTRITION IN MAMMALS AND BIRDS |
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Biological Reviews,
Volume 35,
Issue 3,
1960,
Page 324-361
P. N. WILSON,
D. F. OSBOURN,
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ISSN:1464-7931
DOI:10.1111/j.1469-185X.1960.tb01327.x
出版商:Blackwell Publishing Ltd
年代:1960
数据来源: WILEY
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3. |
ADDENDUM |
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Biological Reviews,
Volume 35,
Issue 3,
1960,
Page 361-363
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ISSN:1464-7931
DOI:10.1111/j.1469-185X.1960.tb01328.x
出版商:Blackwell Publishing Ltd
年代:1960
数据来源: WILEY
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4. |
THE CYTOLOGY OF WOUND HEALING OF BODY SURFACES IN MAMMALS |
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Biological Reviews,
Volume 35,
Issue 3,
1960,
Page 364-410
F. R. JOHNSON,
R. M. H. McMINN,
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摘要:
SUMMARY1The cytological aspects of the repair of wounds with loss of substance in the skin, cornea and a number of mucous, serous and synovial membranes in mammals (laboratory animals and man) have been reviewed.2It is emphasized that, as in the last century, the majority of studies of wound healing continue to be carried out on skin, and the need for examining repair processes in other organs is stressed.3While most of the evidence indicates that epithelium regenerates from old epithelium at the wound margin, the surfaces of serous and synovial membranes are probably repaired by metaplasia of underlying connective tissue cells, assisted by the implantation of islands of surface cells that have desquamated from adjacent surfaces.4The epithelia of the gall‐bladder and urinary bladder (in the cat) display abundant evidence of mitosis in migrating cells. Mitosis in spreading cells has also been observed in ileal and rectal epithelium.5While migration remains a primary factor in epithelial repair, the role of mitosis has possibly been underestimated in the past.6The origin of the connective tissue cells of granulation tissue remains an enigma. There is evidence suggesting that the fibrocytes of the dermis do not proliferate, and that new connective tissue cells are haematogenous in origin.7The endothelial (vascular and lymphatic) elements of granulation tissue originate by budding from pre‐existing vessels. There is doubt whether mitosis occurs in such endothelial cells.8In the repair of mucous membranes in the alimentary tract, new gland formation is observed regularly in the stomach, duodenum and ileum in all the species that have been investigated, including man. The colon and rectum appear to exhibit less regenerative capacity than higher levels of the alimentary tract, for there is no consistent evidence for new gland formation in these viscera.9No universally applicable explanation is yet forthcoming for the accumulation of glycogen that can be detected histochemically in many, but not all, of the regenerating epithelia that have so far been studied.10Among the urgent items on which cytological research might be prosecuted in the future are: the possible role of metaplasia of connective tissue cells in the production of new epithelium, mitosis in migrating epithelium, the factors regulating the initiation and cessation of mitosis, the problem of the origin of new connective tissue cells, and the causes of contraction. Compared with the number of purely morphological studies, histochemistry and autoradiography have not often been wedded to the problems of repair, while the whole field of wound healing at the cellular level awaits study with the electron microsc
ISSN:1464-7931
DOI:10.1111/j.1469-185X.1960.tb01329.x
出版商:Blackwell Publishing Ltd
年代:1960
数据来源: WILEY
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5. |
ADDENDUM |
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Biological Reviews,
Volume 35,
Issue 3,
1960,
Page 410-412
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PDF (185KB)
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ISSN:1464-7931
DOI:10.1111/j.1469-185X.1960.tb01330.x
出版商:Blackwell Publishing Ltd
年代:1960
数据来源: WILEY
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