Neonatal Subarachnoid Hemorrhage Disrupts Multiple Aspects of Cerebellar Development

Over the past decade, survival rates for extremely low gestational age neonates (ELGANs; <28 weeks gestation) has markedly improved. Unfortunately, a significant proportion of ELGANs will suffer from neurodevelopmental dysfunction. Cerebellar hemorrhagic injury (CHI) has been increasingly recognized in the ELGANs population and may contribute to neurologic dysfunction; however, the underlying mechanisms are poorly understood. To address this gap in knowledge, we developed a novel model of early isolated posterior fossa subarachnoid hemorrhage (SAH) in neonatal mice and investigated both acute and long-term effects. Following SAH on postnatal day 6 (P6), we found significant decreased levels of proliferation with the external granular layer (EGL), thinning of the EGL, decreased Purkinje cell (PC) density, and increased Bergmann glial (BG) fiber crossings at P8. At P42, CHI resulted in decreased PC density, decreased molecular layer interneuron (MLI) density, and increased BG fiber crossings. Results from both Rotarod and inverted screen assays did not demonstrate significant effects on motor strength or learning at P35-38. Treatment with the anti-inflammatory drug Ketoprofen did not significantly alter our findings after CHI, suggesting that treatment of neuro-inflammation does not provide significant neuroprotection post CHI. Further studies are required to fully elucidate the mechanisms through which CHI disrupts cerebellar developmental programming in order to develop therapeutic strategies for neuroprotection in ELGANs.

[1]  V. Chizhikov,et al.  Cerebellar development after preterm birth , 2022, Frontiers in Cell and Developmental Biology.

[2]  A. Righini,et al.  Prenatal Diagnosis and Neurodevelopmental Outcome in Isolated Cerebellar Hypoplasia of Suspected Hemorrhagic Etiology: a Retrospective Cohort Study , 2021, The Cerebellum.

[3]  C. Limperopoulos,et al.  Cerebellar injury in premature neonates: Imaging findings and relationship with outcome. , 2021, Seminars in perinatology.

[4]  L. Vetri,et al.  Cerebellum and Prematurity: A Complex Interplay Between Disruptive and Dysmaturational Events , 2021, Frontiers in Systems Neuroscience.

[5]  R. Sillitoe,et al.  Abnormal Cerebellar Development in Autism Spectrum Disorders , 2021, Developmental Neuroscience.

[6]  V. Chizhikov,et al.  Intrauterine growth restriction compromises cerebellar development by affecting radial migration of granule cells via the JamC/Pard3a molecular pathway , 2020, Experimental Neurology.

[7]  R. Sillitoe,et al.  Interactions Between Purkinje Cells and Granule Cells Coordinate the Development of Functional Cerebellar Circuits , 2020, Neuroscience.

[8]  Qin Zhang,et al.  Control of , 2021, Agriculture Automation and Control.

[9]  R. Hawkes,et al.  Origins, Development, and Compartmentation of the Granule Cells of the Cerebellum , 2021, Frontiers in Neural Circuits.

[10]  R. Buddington,et al.  Effects of Phosphatidylserine Source of Docosahexaenoic Acid on Cerebellar Development in Preterm Pigs , 2020, Brain sciences.

[11]  J. Kim,et al.  Preterm Birth Impedes Structural and Functional Development of Cerebellar Purkinje Cells in the Developing Baboon Cerebellum , 2020, bioRxiv.

[12]  M. Benders,et al.  Preterm infants with isolated cerebellar hemorrhage show bilateral cortical alterations at term equivalent age , 2020, Scientific Reports.

[13]  J. Ramirez,et al.  Presynaptic Mechanisms and KCNQ Potassium Channels Modulate Opioid Depression of Respiratory Drive , 2019, Front. Physiol..

[14]  I. Krantz,et al.  Redefining the Etiologic Landscape of Cerebellar Malformations. , 2019, American journal of human genetics.

[15]  L. D. de Vries,et al.  The CHOPIn Study: a Multicenter Study on Cerebellar Hemorrhage and Outcome in Preterm Infants , 2019, The Cerebellum.

[16]  F. Mosca,et al.  Cerebellar Hemorrhage in Preterm Infants: A Meta-Analysis on Risk Factors and Neurodevelopmental Outcome , 2019, Front. Physiol..

[17]  A. Barkovich,et al.  Cerebellar hypoplasia of prematurity: Causes and consequences. , 2019, Handbook of clinical neurology.

[18]  V. Gallo,et al.  Neonatal brain injury causes cerebellar learning deficits and Purkinje cell dysfunction , 2018, Nature Communications.

[19]  V. Gallo,et al.  Neonatal brain injury causes cerebellar learning deficits and Purkinje cell dysfunction , 2018, Nature Communications.

[20]  C. Chiang,et al.  Bergmann glial Sonic hedgehog signaling activity is required for proper cerebellar cortical expansion and architecture. , 2018, Developmental biology.

[21]  V. Chizhikov,et al.  Preterm birth disrupts cerebellar development by affecting granule cell proliferation program and Bergmann glia , 2018, Experimental Neurology.

[22]  V. Chizhikov,et al.  A Phosphatidylserine Source of Docosahexanoic Acid Improves Neurodevelopment and Survival of Preterm Pigs , 2018, Nutrients.

[23]  A. Joyner,et al.  Age-dependent dormant resident progenitors are stimulated by injury to regenerate Purkinje neurons , 2018, bioRxiv.

[24]  J. Lerch,et al.  Systemic inflammation combined with neonatal cerebellar haemorrhage aggravates long-term structural and functional outcomes in a mouse model , 2017, Brain, Behavior, and Immunity.

[25]  S. Takashima,et al.  Neuroimaging and neuropathological characteristics of cerebellar injury in extremely low birth weight infants , 2017, Brain and Development.

[26]  J. Delgado-García,et al.  Compromised Survival of Cerebellar Molecular Layer Interneurons Lacking GDNF Receptors GFRα1 or RET Impairs Normal Cerebellar Motor Learning , 2017, Cell reports.

[27]  H. Vaudry,et al.  Postnatal Migration of Cerebellar Interneurons , 2017, Brain sciences.

[28]  Catherine Limperopoulos,et al.  Structure-function relationships in the developing cerebellum: Evidence from early-life cerebellar injury and neurodevelopmental disorders. , 2016, Seminars in fetal & neonatal medicine.

[29]  Catherine J. Stoodley,et al.  Cerebro-cerebellar circuits in autism spectrum disorder , 2015, Front. Neurosci..

[30]  C. Chiang,et al.  The Purkinje neuron: A central orchestrator of cerebellar neurogenesis , 2015, Neurogenesis.

[31]  E. Fucà,et al.  Sonic hedgehog patterning during cerebellar development , 2015, Cellular and Molecular Life Sciences.

[32]  Aleksandra Badura,et al.  The Cerebellum, Sensitive Periods, and Autism , 2014, Neuron.

[33]  Nicolas Guizard,et al.  Injury to the premature cerebellum: outcome is related to remote cortical development. , 2014, Cerebral cortex.

[34]  Vijay N. Tiwari,et al.  In vivo detection of reduced Purkinje cell fibers with diffusion MRI tractography in children with autistic spectrum disorders , 2014, Front. Hum. Neurosci..

[35]  T. Kemper,et al.  Regional Alterations in Purkinje Cell Density in Patients with Autism , 2014, PloS one.

[36]  D. Goldowitz,et al.  The effect of hemorrhage on the development of the postnatal mouse cerebellum , 2014, Experimental Neurology.

[37]  C. Studholme,et al.  Systemic glycerol decreases neonatal rabbit brain and cerebellar growth independent of intraventricular hemorrhage , 2013, Pediatric Research.

[38]  Chuanming Hao,et al.  The Purkinje neuron acts as a central regulator of spatially and functionally distinct cerebellar precursors. , 2013, Developmental cell.

[39]  C. Pierson,et al.  Cerebellar hemorrhagic injury in premature infants occurs during a vulnerable developmental period and is associated with wider neuropathology , 2013, Acta neuropathologica communications.

[40]  John L.R. Rubenstein,et al.  Patterning and Cell Type Specification in the Developing CNS and PNS , 2013 .

[41]  N. Ohno,et al.  Chapter 11 – Cerebellar Patterning , 2013 .

[42]  A. Schmidt,et al.  Indicators for acute hypoxia--an immunohistochemical investigation in cerebellar Purkinje-cells. , 2012, Forensic science international.

[43]  P. Stanton,et al.  Novel organotypic in vitro slice culture model for intraventricular hemorrhage of premature infants , 2012, Journal of neuroscience research.

[44]  C. Lal,et al.  Cerebellar hemorrhage: a major morbidity in extremely preterm infants , 2012, Journal of Perinatology.

[45]  Y. Yung,et al.  Lysophosphatidic Acid Signaling May Initiate Fetal Hydrocephalus , 2011, Science Translational Medicine.

[46]  Pierre Gressens,et al.  Preterm Delivery Disrupts the Developmental Program of the Cerebellum , 2011, PloS one.

[47]  Nicolas Guizard,et al.  Cerebellar Injury in the Premature Infant Is Associated With Impaired Growth of Specific Cerebral Regions , 2010, Pediatric Research.

[48]  L. Papile Cerebellar Injury in Preterm Infants: Incidence and Findings on US and MR Images , 2010 .

[49]  J. Volpe Cerebellum of the Premature Infant: Rapidly Developing, Vulnerable, Clinically Important , 2009, Journal of child neurology.

[50]  F. Walther,et al.  Cerebellar injury in preterm infants: incidence and findings on US and MR images. , 2009, Radiology.

[51]  A. Dunaevsky,et al.  Morphogenesis and regulation of Bergmann glial processes during Purkinje cell dendritic spine ensheathment and synaptogenesis , 2008, Glia.

[52]  F. Cowan,et al.  Cerebellar cleft: a form of prenatal cerebellar disruption. , 2008, Neuropediatrics.

[53]  Catherine Limperopoulos,et al.  Does Cerebellar Injury in Premature Infants Contribute to the High Prevalence of Long-term Cognitive, Learning, and Behavioral Disability in Survivors? , 2007, Pediatrics.

[54]  Chiara Nosarti,et al.  Impaired executive functioning in young adults born very preterm , 2007, Journal of the International Neuropsychological Society.

[55]  C. Schmitz,et al.  Moderate loss of cerebellar Purkinje cells after chronic bilateral common carotid artery occlusion in rats , 2007, Acta Neuropathologica.

[56]  R. Hausmann,et al.  Hypoxic changes in Purkinje cells of the human cerebellum , 2007, International Journal of Legal Medicine.

[57]  J. Bodensteiner,et al.  Frequency and Nature of Cerebellar Injury in the Extremely Premature Survivor with Cerebral Palsy , 2005, Journal of child neurology.

[58]  Andrew P McMahon,et al.  Sonic hedgehog signaling is required for expansion of granule neuron precursors and patterning of the mouse cerebellum. , 2004, Developmental biology.

[59]  P. Thuras,et al.  Purkinje Cell Size Is Reduced in Cerebellum of Patients with Autism , 2002, Cellular and Molecular Neurobiology.

[60]  R. Buist,et al.  Periventricular/Intraventricular Hemorrhage in Neonatal Mouse Cerebrum , 2003, Journal of neuropathology and experimental neurology.

[61]  J. Strahlendorf,et al.  Hypoxia induces an excitotoxic-type of dark cell degeneration in cerebellar Purkinje neurons , 2001, Neuroscience Research.

[62]  L. Seress,et al.  Cell formation in the cortical layers of the developing human cerebellum , 2001, International Journal of Developmental Neuroscience.

[63]  Masahiko Watanabe,et al.  Dynamic transformation of Bergmann glial fibers proceeds in correlation with dendritic outgrowth and synapse formation of cerebellar Purkinje cells , 2000, The Journal of comparative neurology.

[64]  A. Ruiz i Altaba,et al.  Sonic hedgehog regulates the growth and patterning of the cerebellum. , 1999, Development.

[65]  M. Scott,et al.  Control of Neuronal Precursor Proliferation in the Cerebellum by Sonic Hedgehog , 1999, Neuron.

[66]  M. Berciano,et al.  Reactive gliosis of immature Bergmann glia and microglial cell activation in response to cell death of granule cell precursors induced by methylazoxymethanol treatment in developing rat cerebellum , 1998, Anatomy and Embryology.

[67]  J. Goldman,et al.  Developmental fates and migratory pathways of dividing progenitors in the postnatal rat cerebellum , 1996, The Journal of comparative neurology.

[68]  Richard J Smeyne,et al.  Local Control of Granule Cell Generation by Cerebellar Purkinje Cells , 1995, Molecular and Cellular Neuroscience.

[69]  P. Rakić,et al.  Neuron‐glia relationship during granule cell migration in developing cerebellar cortex. A Golgi and electonmicroscopic study in Macacus rhesus , 1971, The Journal of comparative neurology.

[70]  W. Kondziella [A NEW METHOD FOR THE MEASUREMENT OF MUSCLE RELAXATION IN WHITE MICE]. , 1964, Archives internationales de pharmacodynamie et de therapie.