Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989;75(2):317-26.
doi: 10.1007/BF00247937.

Human fetal spinal cord xenografts survive in the eye of athymic nude rat hosts

Affiliations

Human fetal spinal cord xenografts survive in the eye of athymic nude rat hosts

A F Henschen et al. Exp Brain Res. 1989.

Abstract

Human fetal spinal cord tissue was recovered from elective abortions and grafted to the anterior chamber of the eye of adult athymic nude rats. The transplants slowly became vascularized from the host iris during the first months. There was a clear cut stage-dependent survival and growth along a more "human" time-table. Fetal spinal cord tissue from embryos younger than gestational week 8 showed a much better survival and growth than tissue from older stages. Using laminin immunohistochemistry blood vessels could be visualized in the grafts. The pattern of vascularization was, however, clearly abnormal; there were fewer vessels which had abnormally thick walls as compared to those in the normal spinal cord. Similar to rat spinal cord allografts the human spinal cord xenografts displayed a relative gliosis and were surrounded by a glial layer visualized with antibodies against glial fibrillary acidic protein. Neurofilament-immunoreactive fibres were found inside the glial layer. A variety of neurons were found including large polygonal motoneuron-shaped cells, albeit with CGRP and AChE negative cell bodies. Both Substance P and enkephalin-immunoreactive cells and fibres were found. It is concluded that xenografted fetal human spinal cord survives, grows and may provide a useful model for experimental studies of human spinal cord development and connectivity.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Gen Cytochem Methods. 1958;1:399-422 - PubMed
    1. Neuroscience. 1988 Jul;26(1):193-213 - PubMed
    1. Exp Brain Res. 1985;60(1):38-47 - PubMed
    1. Brain Res. 1986 Jul;393(1):75-84 - PubMed
    1. Proc Natl Acad Sci U S A. 1987 Aug;84(16):5957-61 - PubMed

Publication types

Substances

LinkOut - more resources