Literature DB >> 2912747

Differentiation of substantia gelatinosa-like regions in intraspinal and intracerebral transplants of embryonic spinal cord tissue in the rat.

L B Jakeman1, P J Reier, B S Bregman, E B Wade, M Dailey, R J Kastner, B T Himes, A Tessler.   

Abstract

The differentiation of intracerebral and intraspinal transplants of fetal (E14-E15) rat spinal cord was studied to determine the extent to which myelin-free zones in these embryonic grafts exhibit cytological features and immunocytochemical characteristics of the substantia gelatinosa (SG) of the normal spinal cord. Immunocytochemical staining with antiserum to myelin basic protein (MBP) revealed myelin-free areas of varying proportions within fetal spinal cord grafts. These regions were identified in both newborn and adult recipients regardless of whether donor tissue was grafted to heterotopic (intracerebral) or homotopic (intraspinal) sites. As in the SG of the intact spinal cord, the myelin-free regions consisted mainly of small (7-15 microns) diameter neurons. At the ultrastructural level, these cells were surrounded by a neuropil composed of numerous small caliber, unmyelinated axons and intermediate-sized dendrites. Synaptic terminals in these areas were primarily characterized by the presence of clear, round vesicles, although granular vesicles were occasionally found within these terminals. Immunocytochemical staining demonstrated met- and leu-enkephalin-, neurotensin-, substance P-, and somatostatin-like immunoreactive elements within these myelin-free areas. Thus, regions within embryonic spinal cord grafts undergo some topographical differentiation which parallels that of the normal superficial dorsal horn. The presence of SG-like regions illustrates the potential capacity of fetal spinal cord transplants for replacing some intraspinal neuronal populations at the site of a spinal cord injury in neonatal and adult animals. These graft regions may serve as a source of intersegmental projection neurons or establish an extensive intrinsic circuitry similar to that seen in the normal SG. In addition, the definition of these areas provides a useful model to study the innervation patterns of host axons that typically project to the substantia gelatinosa of the normal spinal cord.

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Year:  1989        PMID: 2912747     DOI: 10.1016/0014-4886(89)90181-7

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  13 in total

1.  Neuronal progenitor transplantation and respiratory outcomes following upper cervical spinal cord injury in adult rats.

Authors:  Todd E White; Michael A Lane; Milapjit S Sandhu; Barbara E O'Steen; David D Fuller; Paul J Reier
Journal:  Exp Neurol       Date:  2010-06-18       Impact factor: 5.330

2.  The Therapeutic Effectiveness of Delayed Fetal Spinal Cord Tissue Transplantation on Respiratory Function Following Mid-Cervical Spinal Cord Injury.

Authors:  Chia-Ching Lin; Sih-Rong Lai; Yu-Han Shao; Chun-Lin Chen; Kun-Ze Lee
Journal:  Neurotherapeutics       Date:  2017-07       Impact factor: 7.620

3.  Integration of Transplanted Neural Precursors with the Injured Cervical Spinal Cord.

Authors:  Victoria M Spruance; Lyandysha V Zholudeva; Kristiina M Hormigo; Margo L Randelman; Tatiana Bezdudnaya; Vitaliy Marchenko; Michael A Lane
Journal:  J Neurotrauma       Date:  2018-04-24       Impact factor: 5.269

4.  Transplantation of Neural Progenitors and V2a Interneurons after Spinal Cord Injury.

Authors:  Lyandysha V Zholudeva; Nisha Iyer; Liang Qiang; Victoria M Spruance; Margo L Randelman; Nicholas W White; Tatiana Bezdudnaya; Itzhak Fischer; Shelly E Sakiyama-Elbert; Michael A Lane
Journal:  J Neurotrauma       Date:  2018-08-10       Impact factor: 5.269

Review 5.  Repair of spinal cord injury with neuronal relays: From fetal grafts to neural stem cells.

Authors:  Joseph F Bonner; Oswald Steward
Journal:  Brain Res       Date:  2015-01-12       Impact factor: 3.252

6.  Fetal spinal cord transplants support growth of supraspinal and segmental projections after cervical spinal cord hemisection in the neonatal rat.

Authors:  P S Diener; B S Bregman
Journal:  J Neurosci       Date:  1998-01-15       Impact factor: 6.167

7.  Intraspinal transplantation and modulation of donor neuron electrophysiological activity.

Authors:  Kun-Ze Lee; Michael A Lane; Brendan J Dougherty; Lynne M Mercier; Milapjit S Sandhu; Justin C Sanchez; Paul J Reier; David D Fuller
Journal:  Exp Neurol       Date:  2013-11-02       Impact factor: 5.330

Review 8.  The Neuroplastic and Therapeutic Potential of Spinal Interneurons in the Injured Spinal Cord.

Authors:  Lyandysha V Zholudeva; Liang Qiang; Vitaliy Marchenko; Kimberly J Dougherty; Shelly E Sakiyama-Elbert; Michael A Lane
Journal:  Trends Neurosci       Date:  2018-07-17       Impact factor: 13.837

9.  Choosing the right cell for spinal cord repair.

Authors:  Lyandysha V Zholudeva; Michael A Lane
Journal:  J Neurosci Res       Date:  2018-11-01       Impact factor: 4.164

10.  Preparation of Neural Stem Cells and Progenitors: Neuronal Production and Grafting Applications.

Authors:  Lyandysha V Zholudeva; Ying Jin; Liang Qiang; Michael A Lane; Itzhak Fischer
Journal:  Methods Mol Biol       Date:  2021
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