scholarly journals A Generative Growth Model for Thalamocortical Axonal Branching in Primary Visual Cortex

2018 ◽  
Author(s):  
Pegah Kassraian Fard ◽  
Michael Pfeiffer ◽  
Roman Bauer

AbstractAxonal morphology displays large variability and complexity, yet the canonical regularities of the cortex suggest that such wiring is based on the repeated initiation of a small set of genetically encoded rules. Extracting underlying developmental principles can hence shed light on what genetically encoded instructions must be available during cortical development. Within a generative model, we investigate growth rules for axonal branching patterns in cat area 17, originating from the lateral geniculate nucleus of the thalamus. This target area of synaptic connections is characterized by extensive ramifications and a high bouton density, characteristics thought to preserve the spatial resolution of receptive fields and to enable connections for the ocular dominance columns. We compare individual and global statistics, such as a newly introduced asymmetry index and the global segment-length distribution, of generated and real branching patterns as the benchmark for growth rules. We show that the proposed model surpasses the statistical accuracy of the Galton-Watson model, which is the most commonly employed model for biological growth processes. In contrast to the Galton-Watson model, our model can recreate the log-normal segment-length distribution of the experimental dataset and is considerably more accurate in recreating individual axonal morphologies. To provide a biophysical interpretation for statistical quantifications of the axonal branching patterns, the generative model is ported into the physically accurate simulation framework of Cx3D. In this simulation environment we demonstrate how the proposed growth process can be formulated as an interactive process between genetic growth rules and chemical cues in the local environment.

Genetics ◽  
2000 ◽  
Vol 154 (1) ◽  
pp. 323-332
Author(s):  
David Waddington ◽  
Anthea J Springbett ◽  
David W Burt

Abstract Comparative genetic maps of two species allow insights into the rearrangements of their genomes since divergence from a common ancestor. When the map details the positions of genes (or any set of orthologous DNA sequences) on chromosomes, syntenic blocks of one or more genes may be identified and used, with appropriate models, to estimate the number of chromosomal segments with conserved content conserved between species. We propose a model for the distribution of the lengths of unobserved segments on each chromosome that allows for widely differing chromosome lengths. The model uses as data either the counts of genes in a syntenic block or the distance between extreme members of a block, or both. The parameters of the proposed segment length distribution, estimated by maximum likelihood, give predictions of the number of conserved segments per chromosome. The model is applied to data from two comparative maps for the chicken, one with human and one with mouse.


2010 ◽  
Vol 518 (22) ◽  
pp. 4649-4673 ◽  
Author(s):  
Anushree Tripathi ◽  
Lucía Prensa ◽  
Carolina Cebrián ◽  
Elisa Mengual

2011 ◽  
Vol 31 (8) ◽  
pp. 3016-3031 ◽  
Author(s):  
S. Karino ◽  
P. H. Smith ◽  
T. C. T. Yin ◽  
P. X. Joris

1985 ◽  
Vol 18 (1) ◽  
pp. 32-44 ◽  
Author(s):  
John A. Miller ◽  
Shaow B. Lin ◽  
Kirk K. S. Hwang ◽  
K. S. Wu ◽  
P. E. Gibson ◽  
...  

2020 ◽  
Vol 21 (10) ◽  
Author(s):  
David Eldred-Evans ◽  
Henry Tam ◽  
Andrew P. T. Smith ◽  
Mathias Winkler ◽  
Hashim U. Ahmed

Abstract Purpose of Review Rapid advances in imaging of the prostate have facilitated the development of focal therapy and provided a non-invasive method of estimating tumour volume. Focal therapy relies on an accurate estimate of tumour volume for patient selection and treatment planning so that the optimal energy dose can be delivered to the target area(s) of the prostate while minimising toxicity to surrounding structures. This review provides an overview of different imaging modalities which may be used to optimise tumour volume assessment and critically evaluates the published evidence for each modality. Recent Findings Multi-parametric MRI (mp-MRI) has become the standard tool for patient selection and guiding focal therapy treatment. The current evidence suggests that mp-MRI may underestimate tumour volume, although there is a large variability in results. There remain significant methodological challenges associated with pathological processing and accurate co-registration of histopathological data with mp-MRI. Advances in different ultrasound modalities are showing promise but there has been limited research into tumour volume estimation. The role of PSMA PET/CT is still evolving and further investigation is needed to establish if this is a viable technique for prostate tumour volumetric assessment. Summary mp-MRI provides the necessary tumour volume information required for selecting patients and guiding focal therapy treatment. The potential for underestimation of tumour volume should be taken into account and an additional margin applied to ensure adequate treatment coverage. At present, there are no other viable image-based alternatives although advances in new technologies may refine volume estimations in the future.


1985 ◽  
Vol 53 (3) ◽  
pp. 759-772 ◽  
Author(s):  
S. F. Morrison ◽  
G. L. Gebber

We studied axonal branching patterns and funicular trajectories of cat medullary raphespinal neurons with spontaneous activity related to inferior cardiac postganglionic sympathetic nerve discharge (as demonstrated with spike-triggered averaging). These neurons were excited by raising carotid sinus pressure. We have classified these neurons as sympathoinhibitory in function and refer to them here as RS neurons. Microstimulation of the second thoracic spinal segment (T2) antidromically activated RS neurons (as determined with time-controlled collision of spontaneous and evoked action potentials). The longest-latency antidromic responses were elicited with the lowest-threshold current from sites in the intermediolateral nucleus (IML). This observation suggests that RS neurons innervated IML. Most RS neurons activated from T2 were also antidromically activated by stimulation of a more caudal thoracic spinal segment (T6 or T12). Time-controlled collision of action potentials evoked by stimulation at two thoracic levels allowed us to distinguish activation of an axonal branch in T2 from that of the main axon coursing through T2 to the more caudal thoracic level. Of those RS axons that branched in T2, 78% descended at least as far caudal as T6, whereas 65% reached T12. The axonal projections of other RS neurons that innervated T2 were restricted to no more than two consecutive thoracic spinal segments (as determined by stimulation in T3). Antidromic mapping of T2 further revealed that the axons of RS neurons coursed through the dorsolateral, ventral, or ventrolateral funiculus to innervate the ipsilateral and/or contralateral IML. The conduction velocities of dorsolateral and ventral RS axons indicated that they were finely myelinated. The data demonstrate the existence of RS neurons with restricted and widespread axonal branching patterns, thereby supporting the view that the medullary raphe complex is capable of regional as well as global inhibitory control over spinal sympathetic outflow.


2014 ◽  
Vol 86 (9) ◽  
pp. 1532-1532
Author(s):  
S. G. Maerten ◽  
M. A. Liauw ◽  
K. Böhm ◽  
A. M. Subhani ◽  
T. E. Müller

2012 ◽  
Vol 218 (5) ◽  
pp. 1133-1157 ◽  
Author(s):  
Anushree Tripathi ◽  
Lucía Prensa ◽  
Elisa Mengual

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