Morphometric study of the development of Purkinje cell dendritic trees in the mouse using vertex analysis

Vertices are the points in an arborescence which interconnect segments and comprise terminal or pendant vertices (Vp), nodal or branching points and the root point. Branching points may be dichotomous (Vd) or trichomtomous (Vt), etc., and are subdivided into distinct two‐dimensional topological entities according to the number of terminal vertices they drain, i.e. Vds comprise primary vertices (Va), connecting two Vps; secondary vertices (Vb), connecting one Vp and one Vd or one Vt; and tertiary vertices (Vc), connecting either two Vds, two Vts or one Vt and one Vd. The four types of Vt (Va‘, Vb’, Vc‘, Vd’) similarly connect three, two, one and zero Vps respectively. Each Vt may be transformed into two Vds thus, Va' = Va + Vb; Vb’ = Va/3 + 4Vb/3 + Vc/3; Vc' = Vb + Vc and Vd’ = 2Vc. Analysis proceeds by transforming mixed trees containing varying proportions of Vds and Vts into entirely dichotomous branching structures. The topology is then defined by the Va Vb ratio which has a unique value according to the mode of growth and the frequency of Vts.

[1]  Sholl Da Dendritic organization in the neurons of the visual and motor cortices of the cat. , 1953 .

[2]  J. Changeux,et al.  Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks , 1976, Nature.

[3]  G. Lynch,et al.  Neuroplasticity in the hippocampal formation. , 1978, Progress in brain research.

[4]  J. Legrand Morphogenetic actions of thyroid hormones , 1979, Trends in Neurosciences.

[5]  A. Riesen,et al.  Evironmental effects on cortical dendritic fields. I. Rearing in the dark. , 1968, Journal of anatomy.

[6]  Gary M. Weiss,et al.  Evidence for loss of Purkinje cell dendrites during late development: A morphometric Golgi analysis in the mouse , 1978, Brain Research.

[7]  M. Berry,et al.  Environmental and genetic determinants of connectivity in the central nervous system--an approach through dendritic field analysis. , 1978, Progress in brain research.

[8]  M. Berry,et al.  Adaption of the cerebellum to deafferentation. , 1980, Progress in brain research.

[9]  M. Berry,et al.  Network analysis of dendritic fields of pyramidal cells in neocortex and Purkinje cells in the cerebellum of the rat. , 1975, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[10]  G. J. Smit,et al.  Quantitative analysis of the cerebral cortex. I. Aselectivity of the Golgi-Cox staining technique. , 1969, Brain research.

[11]  Dendritic field analysis--a reappraisal. , 1972, T.-I.-T. journal of life sciences.

[12]  M. Berry,et al.  The growth of the dendritic trees of Purkinje cells in the cerebellum of the rat , 1976, Brain Research.

[13]  Martin Berry,et al.  ANALYSIS OF NEURAL NETWORKS , 1981 .

[14]  E. Bierman,et al.  The complex‐shaped ‘perforated’ synapse, a problem in quantitative stereology of the brain , 1983, Journal of microscopy.

[15]  M. Shimada,et al.  H3‐Thymidine autoradiographic studies on the cell proliferation and differentiation in the external and the internal granular layers of the mouse cerebellum , 1966, The Journal of comparative neurology.

[16]  F. Goldby,et al.  The Organisation of the Cerebral Cortex , 1957 .

[17]  M. Berry,et al.  Dendritic growth and the control of neuronal form. , 1980, Current topics in developmental biology.

[18]  M. Berry,et al.  The application of network analysis to the study of branching patterns of large dendritic fields , 1976, Brain Research.

[19]  L. Uzman,et al.  The histogenesis of the mouse cerebellum as studied by its tritiated thymidine uptake , 1960, The Journal of comparative neurology.

[20]  R. Sidman,et al.  An autoradiographic analysis of histogenesis in the mouse cerebellum. , 1961, Experimental neurology.