The University of Southampton
University of Southampton Institutional Repository

Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole-body energy expenditure

Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole-body energy expenditure
Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole-body energy expenditure

The epidermis is the outermost layer of skin that acts as a barrier to protect the body from the external environment and to control water and heat loss. This barrier function is established through the multistage differentiation of keratinocytes and the presence of bioactive sphingolipids such as ceramides, the levels of which are tightly regulated by a balance of ceramide synthase and ceramidase activities. Here we reveal the essential role of alkaline ceramidase 1 (Acer1) in the skin. Acer1-deficient (Acer1(-/-) ) mice showed elevated levels of ceramide in the skin, aberrant hair shaft cuticle formation and cyclic alopecia. We demonstrate that Acer1 is specifically expressed in differentiated interfollicular epidermis, infundibulum and sebaceous glands and consequently Acer1(-/-) mice have significant alterations in infundibulum and sebaceous gland architecture. Acer1(-/-) skin also shows perturbed hair follicle stem cell compartments. These alterations result in Acer1(-/-) mice showing increased transepidermal water loss and a hypermetabolism phenotype with associated reduction of fat content with age. We conclude that Acer1 is indispensable for mammalian skin homeostasis and whole-body energy homeostasis. © 2016 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Alkaline Ceramidase/genetics, Alopecia/enzymology, Animals, Cell Differentiation, Ceramides/metabolism, Energy Metabolism, Epidermis/abnormalities, Female, Hair Follicle/abnormalities, Homeostasis, Humans, Keratinocytes/enzymology, Male, Mice, Mice, Inbred C57BL, Pituitary Gland/abnormalities, Sebaceous Glands/abnormalities, Skin/enzymology, Skin Abnormalities, Sphingolipids/metabolism
1096-9896
374-383
Liakath-Ali, Kifayathullah
8d5a020c-e976-4901-9195-68f4bc0de74e
Vancollie, Valerie E.
f5178931-9739-4c6d-80d7-eb5945d7226b
Lelliott, Christopher J.
af26504c-561c-4afc-9e0e-26de86f3db8c
Speak, Anneliese O.
543d783f-b1c3-4240-b81e-e1a391a84646
Lafont, David
80166eb0-6926-44d6-b70d-e2ff13212d91
Protheroe, Hayley J.
373b472a-d4d7-482e-9ee9-a8579f4767ef
Ingvorsen, Camilla
3ff71918-e41c-470c-905c-b90e69cbe01b
Galli, Antonella
22d064da-2612-4629-9ac3-28cbbe93fba1
Green, Angela
f216a1c1-1f1f-4761-928d-20db76a9c4b9
Gleeson, Diane
bfa4ca50-7310-4f07-a453-ec676719191d
Ryder, Ed
2b4c8c74-eac4-47c7-84b0-13163050ec6a
Glover, Leanne
e87aed09-6c13-4188-b68c-ec37c0f7e4b7
Vizcay-Barrena, Gema
22067f58-0d83-4aad-9857-79f5ad2ebab5
Karp, Natasha A.
db44a20e-44b2-4ae0-9691-45d81bfec9b3
Arends, Mark J.
b4ecb1b5-d0c7-4c5f-ba0c-621137cc7734
Brenn, Thomas
8afc6860-8377-4481-9869-97e9cee8c112
Spiegel, Sarah
9f7f55a2-efff-41c6-8678-aa0af5cc4353
Adams, David J.
d235aadc-722e-471b-805d-c5bda9c0f95e
Watt, Fiona M.
24fff937-94b0-4127-8cbb-e8bd6e01fa29
van der Weyden, Louise
cc645f0d-3773-48c6-9d90-b26a9f8fea06
Liakath-Ali, Kifayathullah
8d5a020c-e976-4901-9195-68f4bc0de74e
Vancollie, Valerie E.
f5178931-9739-4c6d-80d7-eb5945d7226b
Lelliott, Christopher J.
af26504c-561c-4afc-9e0e-26de86f3db8c
Speak, Anneliese O.
543d783f-b1c3-4240-b81e-e1a391a84646
Lafont, David
80166eb0-6926-44d6-b70d-e2ff13212d91
Protheroe, Hayley J.
373b472a-d4d7-482e-9ee9-a8579f4767ef
Ingvorsen, Camilla
3ff71918-e41c-470c-905c-b90e69cbe01b
Galli, Antonella
22d064da-2612-4629-9ac3-28cbbe93fba1
Green, Angela
f216a1c1-1f1f-4761-928d-20db76a9c4b9
Gleeson, Diane
bfa4ca50-7310-4f07-a453-ec676719191d
Ryder, Ed
2b4c8c74-eac4-47c7-84b0-13163050ec6a
Glover, Leanne
e87aed09-6c13-4188-b68c-ec37c0f7e4b7
Vizcay-Barrena, Gema
22067f58-0d83-4aad-9857-79f5ad2ebab5
Karp, Natasha A.
db44a20e-44b2-4ae0-9691-45d81bfec9b3
Arends, Mark J.
b4ecb1b5-d0c7-4c5f-ba0c-621137cc7734
Brenn, Thomas
8afc6860-8377-4481-9869-97e9cee8c112
Spiegel, Sarah
9f7f55a2-efff-41c6-8678-aa0af5cc4353
Adams, David J.
d235aadc-722e-471b-805d-c5bda9c0f95e
Watt, Fiona M.
24fff937-94b0-4127-8cbb-e8bd6e01fa29
van der Weyden, Louise
cc645f0d-3773-48c6-9d90-b26a9f8fea06

Liakath-Ali, Kifayathullah, Vancollie, Valerie E., Lelliott, Christopher J., Speak, Anneliese O., Lafont, David, Protheroe, Hayley J., Ingvorsen, Camilla, Galli, Antonella, Green, Angela, Gleeson, Diane, Ryder, Ed, Glover, Leanne, Vizcay-Barrena, Gema, Karp, Natasha A., Arends, Mark J., Brenn, Thomas, Spiegel, Sarah, Adams, David J., Watt, Fiona M. and van der Weyden, Louise (2016) Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole-body energy expenditure. The Journal of Pathology, 239 (3), 374-383. (doi:10.1002/path.4737).

Record type: Article

Abstract

The epidermis is the outermost layer of skin that acts as a barrier to protect the body from the external environment and to control water and heat loss. This barrier function is established through the multistage differentiation of keratinocytes and the presence of bioactive sphingolipids such as ceramides, the levels of which are tightly regulated by a balance of ceramide synthase and ceramidase activities. Here we reveal the essential role of alkaline ceramidase 1 (Acer1) in the skin. Acer1-deficient (Acer1(-/-) ) mice showed elevated levels of ceramide in the skin, aberrant hair shaft cuticle formation and cyclic alopecia. We demonstrate that Acer1 is specifically expressed in differentiated interfollicular epidermis, infundibulum and sebaceous glands and consequently Acer1(-/-) mice have significant alterations in infundibulum and sebaceous gland architecture. Acer1(-/-) skin also shows perturbed hair follicle stem cell compartments. These alterations result in Acer1(-/-) mice showing increased transepidermal water loss and a hypermetabolism phenotype with associated reduction of fat content with age. We conclude that Acer1 is indispensable for mammalian skin homeostasis and whole-body energy homeostasis. © 2016 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Text
The Journal of Pathology - 2016 - Liakath‐Ali - Alkaline ceramidase 1 is essential for mammalian skin homeostasis and - Version of Record
Available under License Creative Commons Attribution.
Download (4MB)

More information

e-pub ahead of print date: 30 May 2016
Published date: July 2016
Keywords: Alkaline Ceramidase/genetics, Alopecia/enzymology, Animals, Cell Differentiation, Ceramides/metabolism, Energy Metabolism, Epidermis/abnormalities, Female, Hair Follicle/abnormalities, Homeostasis, Humans, Keratinocytes/enzymology, Male, Mice, Mice, Inbred C57BL, Pituitary Gland/abnormalities, Sebaceous Glands/abnormalities, Skin/enzymology, Skin Abnormalities, Sphingolipids/metabolism

Identifiers

Local EPrints ID: 491542
URI: http://eprints.soton.ac.uk/id/eprint/491542
ISSN: 1096-9896
PURE UUID: 8139072b-9a63-4d35-b47b-6a4472bb4cc9
ORCID for Kifayathullah Liakath-Ali: ORCID iD orcid.org/0000-0001-9047-7424

Catalogue record

Date deposited: 25 Jun 2024 17:09
Last modified: 26 Jun 2024 02:11

Export record

Altmetrics

Contributors

Author: Kifayathullah Liakath-Ali ORCID iD
Author: Valerie E. Vancollie
Author: Christopher J. Lelliott
Author: Anneliese O. Speak
Author: David Lafont
Author: Hayley J. Protheroe
Author: Camilla Ingvorsen
Author: Antonella Galli
Author: Angela Green
Author: Diane Gleeson
Author: Ed Ryder
Author: Leanne Glover
Author: Gema Vizcay-Barrena
Author: Natasha A. Karp
Author: Mark J. Arends
Author: Thomas Brenn
Author: Sarah Spiegel
Author: David J. Adams
Author: Fiona M. Watt
Author: Louise van der Weyden

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×