Analysis of neural progenitor cells in premature infant CSF (v1)

  • Research type

    Research Study

  • Full title

    Analysis of neural progenitor cells in premature infant cerebrospinal fluid

  • IRAS ID

    178943

  • Contact name

    Axel Heep

  • Contact email

    axel.heep@bristol.ac.uk

  • Sponsor organisation

    Research and Innovation, North Bristol NHS Trust

  • Duration of Study in the UK

    0 years, 11 months, 30 days

  • Research summary

    Background:
    Bleeding into the brain followed by progressive enlargement of the fluid space (ventricles) is one of the most serious complications of preterm birth. Described as intraventricular haemorrhage, this affects approximately one in five infants born under 32 weeks gestation, however there are currently no active therapies we can offer.

    40% of premature infants who develop severe intraventricular haemorrhage will progress to have problems with cerebrospinal fluid (CSF) resorption leading to post-haemorrhagic ventricular dilatation (PHVD). This requires repeated external drainage of CSF via a reservoir inserted into the lateral ventricles. Currently this CSF is discarded. Previous research has demonstrated that this CSF contains significant numbers of neural progenitor cells.

    Neural progenitor cells isolated at this stage of development provide a unique opportunity to augment the endogenous repair mechanisms in these preterm infants and for treatment of diverse neurodegenerative diseases.

    Aims:
    The aim of this project is to isolate and further characterise neural progenitor cells from the CSF of premature infants (24-35 weeks gestation) undergoing drainage for PHVD.

    Project:
    Within this initial study we would aim to: analyse the CSF of 5-10 infants; isolate, quantify and characterise neural progenitor cells from the CSF by immunocytochemistry for stem cell markers; expand and differentiate these cells in vitro to investigate their cell fate (e.g. neurons, glia or oligodendrocytes) using immunohistochemical methods and quantitative PCR for specific genes.

  • REC name

    Yorkshire & The Humber - Bradford Leeds Research Ethics Committee

  • REC reference

    15/YH/0251

  • Date of REC Opinion

    22 May 2015

  • REC opinion

    Favourable Opinion