Skip to main content Accessibility help
×
Hostname: page-component-74656f9884-w5jd6 Total loading time: 0 Render date: 2026-11-04T00:54:47.837Z Has data issue: false hasContentIssue false

5 - Bartonella signaling and endothelial cell proliferation

Published online by Cambridge University Press:  15 September 2009

Garret Ihler
Affiliation:
Department of Medical Biochemistry and Genetics, Texas A&M College of Medicine
Anita Verma
Affiliation:
Laboratory of Respiratory and Special Pathogens, DBPAP/CBER, Food and Drug Administration
Javier Arevalo
Affiliation:
Proctor and Gamble America Latina
Alistair J. Lax
Affiliation:
King's College London
Get access

Summary

Bartonella bacilliformis is the causative agent of Carrion's disease (for a recent medical review, see Maguina and Gotuzzo, 2000). B. bacilliformis was in a genus by itself until recent taxonomic revisions associated it with other bacteria. Now there are sixteen known species of Bartonella, of which seven are associated with human disease. B. bacilliformis enters the bloodstream of humans through the bite of an insect vector and targets primarily erythrocytes and endothelial cells.

For many years, it seemed as though important and interesting conclusions about the mechanism of angiogenesis might result from the study of B. bacilliformis, which can initiate and perpetuate lesions formed of proliferating endothelial cells and newly formed capillaries. Since then, the Science juggernaut has moved on, more rapidly for angiogenesis than for Bartonella, and so it now appears that we can best understand B. bacilliformis (and the closely related Bartonella henselae) by reference to the known biology of angiogenesis. However, study of B. bacilliformis has made at least one useful contribution to our knowledge of angiogenesis. Entry of B. bacilliformis by vacuole formation and macropinocytosis was shown to be accomplished by activation of Rho, Rac, and Cdc42 GTPases. This process appeared to be analogous to the angiogenic process by which endothelial cells take in large volumes of extracellular fluids to form large central vacuoles, which perhaps fuse between cells to form the nascent capillary.

Information

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Book purchase

Temporarily unavailable

Save book to Kindle

To save this book to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×