Luxol fast blue stain

From Wikipedia, the free encyclopedia
  (Redirected from LFB stain)
Jump to: navigation, search
Micrograph of the pons using a hematoxylin & eosin-luxol fast blue stain.
Coronal section of a mouse brain stained with Hematoxylin & LFB

Luxol fast blue stain, abbreviated LFB stain or simply LFB, is a commonly used stain to observe myelin under light microscopy, created by Heinrich Klüver and Barrera in 1953.[1] LFB is commonly used to detect demyelination in the central nervous system (CNS), but cannot discern myelination in the peripheral nervous system.[2]

Procedure[edit]

Luxol fast blue is a copper phthalocyanine dye that is soluble in alcohol and is attracted to bases found in the lipoproteins of the myelin sheath.[3][4]

Under the stain, myelin fibers appear blue, neuropil appears pink, and nerve cells appear purple. Tissues sections are treated over an extended period of time (usually overnight) and then differentiated with a lithium carbonate solution.[4]

Combination methods[edit]

The combination of LFB with a variety of common staining methods provides the most useful and reliable method for the demonstration of pathological processes in the CNS.[2] It is often combined with hematoxylin and eosin, which is abbreviated H-E-LFB, H&E-LFB. Other common staining methods include the periodic acid-Schiff, Oil Red O, phosphotungstic acid, and Holmes silver nitrate method.[2]

Disease states[edit]

Studies have demonstrated that in both, human and mice, traumatic brain injury is associated with ongoing white matter degeneration with survival > 1 year post-injury.[5] [6]


See also[edit]

References[edit]

  1. ^ Kluver, H., and Barrera, E. A method for the combined staining of cells and fibers in the Nervous system. J. Neuropath. Exp. Neurol. 12:400-403, 1953.
  2. ^ a b c Shin J. Oh (2002). Color Atlas of Nerve Biopsy Pathology. CRC Press. pp. 191–. ISBN 978-0-8493-1676-0. Retrieved 1 January 2013. 
  3. ^ Bruce-Gregorios, Jocelyn. Histophatologic Techniques. Goodwill Trading Co., Inc. pp. 241–. ISBN 978-971-12-0270-5. Retrieved 1 January 2013. 
  4. ^ a b Peter A. Humphrey; Louis P. Dehner; John D. Pfeifer (2008). The Washington Manual of Surgical Pathology: Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri. Lippincott Williams & Wilkins. pp. 681–. ISBN 978-0-7817-6527-5. Retrieved 1 January 2013. 
  5. ^ Jonhson, VE; Stewart, JE (January 2013). "Inflammation and white matter degeneration persist for years after a single traumatic brain injury.". Brain. 136 (1): 28–42. doi:10.1002/ana.24064. PMID 23365092. 
  6. ^ Mouzon, B; Bachmeier, C (February 2014). "Chronic neuropathological and neurobehavioral changes in a repetitive mild traumatic brain injury model.". Ann Neurol. 75 (2): 241–254. doi:10.1002/ana.24064. PMID 24243523. 
  • Sheehan D, Hrapchak B, Theory and practice of Histotechnology, 2nd ed,1980, pp. 262–264, Battelle Press, Ohio.